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Publication numberUS20090093526 A1
Publication typeApplication
Application numberUS 11/932,397
Publication dateApr 9, 2009
Filing dateOct 31, 2007
Priority dateDec 22, 1997
Also published asUS7517880, US20040102636, US20120270878
Publication number11932397, 932397, US 2009/0093526 A1, US 2009/093526 A1, US 20090093526 A1, US 20090093526A1, US 2009093526 A1, US 2009093526A1, US-A1-20090093526, US-A1-2009093526, US2009/0093526A1, US2009/093526A1, US20090093526 A1, US20090093526A1, US2009093526 A1, US2009093526A1
InventorsScott Miller, Martin Osterhout, Jacques Dumas, Uday Khire, Timothy B. Lowinger, William J. Scott, Roger A. Smith, Jill E. Wood, David E. Gunn, Holia Hatoum-Mokdad, Marell Rodriguez, Robert Sibley, Ming Wang, Tiffany Turner, Catherine Brennan
Original AssigneeScott Miller, Martin Osterhout, Jacques Dumas, Uday Khire, Lowinger Timothy B, Scott William J, Smith Roger A, Wood Jill E, Gunn David E, Holia Hatoum-Mokdad, Marell Rodriguez, Robert Sibley, Ming Wang, Tiffany Turner, Catherine Brennan
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Inhibition of p38 kinase using symmetrical and unsymmetrical diphenyl ureas
US 20090093526 A1
Abstract
This invention relates to the use of a group of aryl ureas in treating cytokine mediated diseases and proteolytic enzyme mediated diseases, and pharmaceutical compositions for use in such therapy.
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Claims(22)
1. A method of treating a disease, other than cancer, mediated by p-38, comprising administering a compound of formula I
wherein
A is
B is a substituted or unsubstituted, up to tricyclic aryl or heteroaryl moiety of up to 30 carbon atoms with at least one 6-member aromatic structure containing 0-4 members of the group consisting of nitrogen, oxygen and sulfur, wherein if B is substituted, it is substituted by one or more substituents selected from the group consisting of halogen, up to per-halo, and Wn, wherein n is 0-3 and each W is independently selected from the group consisting of —CN, —CO2R7, —C(O)NR7R7, —C(O)—R7, —NO2, —OR7, —SR7, —NR7R7, —NR7C(O)OR7, —NR7C(O)R7, C1-C10 alkyl, C1-10-alkenyl, C1-C10-alkoxy, C3-C10 cycloalkyl, C6-C14 aryl, C7-C24 alkaryl, C3-C13 heteroaryl, C4-C23 alkheteroaryl, substituted C1-C10 alkyl, substituted C2-10-alkenyl, substituted C1-10-alkoxy, substituted C3-C10 cycloalkyl, substituted C4-C23 alkheteroaryl and Q-Ar;
wherein if W is a substituted group, it is substituted by one or more substituents independently selected from the group consisting of —CN, —CO2R7, —C(O)R7, —C(O)NR7R7, —OR7, —SR7, —NR7R7, NO2, —NR7C(O)R7, —NR7C(O)OR7 and halogen up to per-halo;
wherein each R7 is independently selected from H, C1-C10 alkyl, C2-10-alkenyl, C3-C10 cycloalkyl, C6-C14 aryl, C3-C13 hetaryl, C7-C24 alkaryl, C4-C23 alkheteroaryl, up to per-halosubstituted C1-C10 alkyl, up to per-halosubstituted C2-10-alkenyl, up to per-halosubstituted C3-C10 cycloalkyl, up to per-halosubstituted C6-C14 aryl and up to per-halosubstituted C3-C13 hetaryl,
wherein Q is —O—, —S—, —N(R7)—, —(CH2)—m, —C(O)—, —CH(OH)—, —(CH2)mO—, —NR7C(O)NR7R7′—, —NR7C(O)—, —C(O)NR7—, —(CH2)mS—, —(CH2)mN(R7)—, —O(CH2)m—, —CHXa, —CXa 2—, —S—(CH2)m— and —N(R7)(CH2)m—,
m=1-3, and Xa is halogen; and
Ar is a 5-10 member aromatic structure containing 0-2 members of the group consisting of nitrogen, oxygen and sulfur, which is unsubstituted or substituted by halogen up to per-halo and optionally substituted by Zn1, wherein n1 is 0 to 3 and each Z is independently selected from the group consisting of —CN, —CO2R7, —C(O)NR7R7, —C(O)—NR7, —COR7, —NO2, —OR7, —SR7, —NR7R7, —NR7C(O)OR7, —NR7C(O)R7, C1-C10 alkyl, C3-C10 cycloalkyl, C6-C14 aryl, C3-C13 hetaryl, C7-C24 alkaryl, C4-C23 alkheteroaryl, substituted C1-C10 alkyl, substituted C3-C10 cycloalkyl, substituted C7-C24 alkaryl and substituted C4-C23 alkheteroaryl; wherein the one or more substituents of Z is selected from the group consisting of —CN, —CO2R7, —C(O)NR7R7, —OR7, —SR7, —NO2, —NR7R7, —NR7C(O)R7, —NR7C(O)OR7,
R3′, R4′, R5′ are each independently H, C1-10-alkyl, optionally substituted by halogen, up to perhalo, C1-10 alkoxy, optionally substituted by halogen, up to perhaloalkoxy, halogen; NO2 or NH2;
R6′ is H, C1-10-alkyl, C1-10 alkoxy, —NHCOR1; —NR1COR1; NO2;
one of R4′, R5′ or R6′ can be —X—Y,
or 2 adjacent R4′-R6′ can together be an aryl or hetaryl ring with 5-12 atoms, optionally substituted by C1-10-alkyl, C1-10 alkoxy, C3-10 cycloalkyl C2-10 alkenyl, C1-10 alkanoyl, C6-12 aryl, C5-12 hetaryl or C6-12 aralkyl;
R1 is C1-10-alkyl optionally substituted by halogen, up to perhalo;
X is —CH2—, —S—, —N(CH3)—, —NHC(O)—, —CH2—S—, —S—CH2—, —C(O)—, or —O—; and
X is additionally a single bond where Y is pyridyl;
Y is phenyl, pyridyl, naphthyl, pyridone, pyrazine, benzodioxane, benzopyridine, pyrimidine or benzothiazole, each optionally substituted by
C1-10-alkyl, C1-10-alkoxy, halogen, OH, —SCH3 or NO2 or, where Y is phenyl, by
or a pharmaceutically acceptable salt thereof.
2. A method according to claim 1, comprising administering a compound of formula Ia
wherein
R3, R4, R5, and R6 are each independently H; halogen; C1-10-alkyl optionally substituted by halogen up to perhalo; C1-10-alkoxy optionally substituted by at least one hydroxy group or halogen up to perhalo, C6-12 aryl, optionally substituted by C1-10 alkoxy or halogen, C5-12 hetaryl, optionally substitued by C1-10 alkyl, C1-100 alkoxy or halogen; NO2; SO2F; —SO2CHpX3-p; —COOR1; —OR1CONHR1; —NHCOR1; —SR1; NH2; —N(SO2R1)2; furyloxy;
2 adjacent R3-R6 can together form an aryl or hetaryl ring with 5-12 atoms, optionally substituted by C1-10-alkyl, C1-10-alkoxy, C3-10-cycloalkyl, C2-10-alkenyl, C1-10-alkanoyl, C6-12-aryl, C5-12-hetaryl, C6-12-aralkyl, C6-12-alkaryl, halogen; —NR1; —NO2; —CF3; —COOR1; —NHCOR1; —CN; —CONR1R1; —SO2R2; —SOR2; —SR2; in which R1 is H or C1-10-alkyl and R2 is C1-10-alkyl optionally substituted by halogen, up to perhalo, with —SO2-optionally incorporated in the aryl or hetaryl ring;
p is 0 or 1;
one of R3, R4, R5 or R6 can be —X—Y,
with the proviso that if R3 and R6 are both H, one of R4 or R5 is not H, and R3′-R6′ are as defined in claim 1.
3. A method according to claim 2, wherein
R3 is H; halogen; C1-10-alkyl optionally substituted by halogen, up to perhalo, NO2, —SO2F or —SO2CF3;
R4 is H, C1-10-alkyl, C1-10-alkoxy, halogen or NO2;
R5 is H, C1-100-alkyl optionally substituted by halogen, up to perhalo;
R6 is H, hydroxy, C1-10-alkoxy optionally substituted by at least one hydroxy group;
—COOR1; —OR1CONHR1; —NHCOR1; —SR1; phenyl optionally substituted by halo
or C1-10-alkoxy; NH2; —N(SO2R1)2, furyloxy, thiophene, pyrole or methyl substituted pyrole,
4. A method according to claim 2, wherein R3 is Cl, F, C4-5-branched alkyl, —SO2F or —SO2CF3; and R6 is hydroxy; C1-10-alkoxy optionally substituted by at least one hydroxy group; —COOR1; —OR1CONHR1; —NHCOR1; —SR1; phenyl optionally substituted by halo or C1-10-alkoxy; NH2; —N(SO2R1)2, furyloxy,
5. A compound according to claim 2, wherein R4′ is C1-10-alkyl or halogen; R5′ is H, C1-10-alkyl, halogen, CF3, halogen, NO2 or NH2; and R6′ is H, C1-10-alkyl, halogen, —NHCOCH3, —N(CH3)COCH3, NO2,
6. A method according to claim 2, wherein R5′ is C1-10-alkyl, halogen, CF3, halogen, NO2 or NH2.
7. A method according to claim 2, wherein R6′ is C1-10-alkyl, halogen, —NHCOCH3, —N(CH3)COCH3, NO2,
8. A method according to claim 4, wherein R3 is t-butyl or CF3 and R6 is —OCH3.
9. A method according to claim 2, wherein the disease is mediated by a cytokine or protease regulated by p38.
10. A method according to claim 2, wherein the disease is mediated by TNFα, MMP-1, MMP-3, IL-1, IL-6 or IL-8.
11. A method according to claim 2, wherein the disease is an inflammatory or immunomodulatory disease.
12. A method according to claim 2, wherein the disease is osteoarthritis, rheumatoid arthritis, osteoporosis, asthma, septic shock, inflammatory bowel disease, or the result of host-versus-graft reactions.
13. A method according to claim 1, wherein the compound of formula I is
N-(5-tert-Butyl-2-methoxyphenyl)-N′-(4-phenyloxphenyl)urea;
N-(5-tert-Butyl-2-methoxyphenyl)-N′-(4-(4-pyridinyloxy)phenyl)urea;
N-(5-Tert-Butyl-2-methoxyphenyl)-N′-(4-(4-pyridinylmethyl)phenyl)urea;
N-(5-tert-Butyl-2-methoxyphenyl)-N′-(4-(4-(4,7-methano-1H-isoindole-1,3(2H)-dionyl)methyl)phenyl)urea;
N-(5-tert-Butyl-2-phenylphenyl)-N′-(2,3-dichlorophenyl)urea;
N-(5-tert-Butyl-2-(3-thienyl)phenyl)-N′-(2,3-dichlorophenyl)urea;
N-(5-tert-Butyl-2-(N-methylaminocarbonyl)methoxyphenyl)-N′-(2,3-dichlorophenyl)urea;
N-(5-tert-Butyl-2-(N-methylaminocarbonyl)methoxyphenyl)-N′-(1-naphthyl)urea;
N-(5-tert-Butyl-2-(N-morpholinocarbonyl)methoxyphenyl)-N′-(2,3-dichlorophenyl)urea;
N-(5-tert-Butyl-2-(N-morpholinocarbonyl)methoxyphenyl)-N′-(1-naphthyl)urea;
N-(5-tert-Butyl-2-methoxyphenyl)-N′-(4-(3-pyridinyl)methylphenyl)urea;
N-(5-tert-Butyl-2-(3-tetrahydrofuranyloxy)phenyl)-N′-(2,3-dichlorophenyl)urea;
N-(5-Trifluoromethyl-2-methoxyphenyl)-N′-(4-methylphenyl)urea;
N-(5-Trifluoromethyl-2-methoxyphenyl)-N′-(4-methyl-2-fluorophenyl)urea;
N-(5-Trifluoromethyl-2-methoxyphenyl)-N′-(4-fluoro-3-chlorophenyl)urea;
N-(5-Trifluoromethyl-2-methoxyphenyl)-N′-(4-methyl-3-chlorophenyl)urea;
N-(5-Trifluoromethyl-2-methoxyphenyl)-N′-(4-methyl-3-fluorophenyl)urea;
N-(5-Trifluoromethyl-2-methoxyphenyl)-N′-(2,4-difluorophenyl)urea;
N-(5-Trifluoromethyl-2-methoxyphenyl)-N′-(4-phenyloxy-3,5-dichlorophenyl)urea;
N-(5-Trifluoromethyl-2-methoxyphenyl)-N′-(4-(4-pyridinylthio)phenyl)urea;
N-(5-Trifluoromethyl-2-methoxyphenyl)-N′-(4-(4-pyridinyloxy)phenyl)urea;
N-(5-Trifluoromethyl-2-methoxyphenyl)-N′-(3-(4-pyridinylthio)phenyl)urea;
N-(5-Trifluoromethyl-2-methoxyphenyl)-N′-(4-(3-(N-methylaminocarbonyl)-phenyloxy)phenyl)-urea;
N-(5-Fluorosulfonyl)-2-methoxyphenyl)-N′-(4-methylphenyl)urea;
N-(5-(Difluoromethanesulfonyl)-2-methoxyphenyl)-N′-(4-methylphenyl)urea;
N-(5-(Difluoromethanesulfonyl)-2-methoxyphenyl)-N′-(4-fluorophenyl)urea;
N-(5-(Difluoromethanesulfonyl)-2-methoxyphenyl)-N′-(4-methyl-2-fluorophenyl)urea;
N-(5-(Difluoromethanesulfonyl)-2-methoxyphenyl)-N′-(4-methyl-3-fluorophenyl)urea;
N-(5-(Difluoromethanesulfonyl)-2-methoxyphenyl)-N′-(4-methyl-3-chlorophenyl)urea;
N-(5-(Difluoromethanesulfonyl)-2-methoxyphenyl)-N′-(4-fluoro-3-chlorophenyl)urea;
N-(5-(Difluoromethanesulfonyl)-2-methoxyphenyl)-N′-(4-fluoro-3-methylphenyl)urea;
N-(5-(Difluoromethanesulfonyl)-2-methoxyphenyl)-N′-(2,3-dimethylphenyl)urea;
N-(5-(Trifluoromethanesulfonyl)-2-methoxphenyl)-N′-(4-methylphenyl)urea;
N-(3-methoxy-2-naphthyl)-N′-(2-fluorophenyl)urea);
N-(3-Methoxy-2-naphthyl)-N′-(4-methylphenyl)urea;
N-(3-Methoxy-2-naphthyl)-N′-(3-fluorophenyl)urea;
N-(3-Methoxy-2-naphthyl)-N′-(4-methyl-3-fluorophenyl)urea;
N-(3-Methoxy-2-naphthyl)-N′-(2,3-dimethylphenyl)urea;
N-(3-Methoxy-2-naphthyl)-N′-(1-naphthyl)urea;
N-(3-Methoxy-2-naphthyl)-N′-(4-(4-pyridinylmethyl)phenyl)urea;
N-(3-Methoxy-2-naphthyl)-N′-(4-(4-pyridinylthio)phenyl)urea;
N-(3-Methoxy-2-naphthyl)-N′-(4-(4-methoxyphenyloxy)phenyl)urea; and
N-(3-Methoxy-2-naphthyl)-N′-(4-(4-(4,7-methano-1H-isoindole-1,3(2H)-dionyl)methyl)phenyl)urea.
N-(2-Hydroxy-4-nitro-5-chlorophenyl)-N′-(phenyl)urea; or
N-(2-Hydroxy-4-nitro-5-chlorophenyl)-N′-(4-(4-pyridinylmethly)phenyl)urea.
14. A compound of formula I
wherein
R3, R4 and R6 are each independently H; halogen; C1-10-alkyl optionally substituted by halogen to perhalo; C1-10-alkoxy optionally substituted by at least one hydroxy group; NO2; SO2F; —SO2CHnX3-n; —COOR1; —OR1CONHR1; —NHCOR1; —SR1; C6-12 aryl, optionally substituted by C1-10-alkyl, C1-10 alkoxy or halogen, C5-12 hetaryl, optionally substitued by C1-10 alkyl, C1-10 alkoxy or halogen; NH2; —N(SO2R1)2; furyloxy;
2 adjacent R3-R6 can together form an aryl or hetaryl ring with 5-12 atoms, optionally substituted by C1-10-alkyl, C1-10-alkoxy, C3-10-cycloalkyl, C2-10-alkenyl, C1-10-alkanoyl, C6-12-aryl, C5-12-hetaryl, C6-12-aralkyl, C6-12-alkaryl, halogen; NR1R1, NO2; —CF3; —COOR1; —NHCOR1; —CN; —CONR1R2; —SO2R2; —SOR2; —SR2; in which R1 is H or C1-10-alkyl and R2 is C1-10-alkyl; C1-10-alkoxy, optionally substituted by halogen up to perhaloalkoxy,
R3′, R4′ and R5′ are each independently H, C1-10-alkyl, optionally substituted by halogen, up to perhalo; halogen; NO2 or NH2;
R6′ is H, C1-10-alkyl, halogen, —NHCOR1; —NR1COR1; NO2;
or 2 adjacent R4′-R6′ can together be an aryl or hetaryl ring with 5-12 atoms;
R1 is C1-10-alkyl;
n is 0 or 1;
X is —CH2—, —S—, N(CH3)—, —NHC(O), CH2—S—, —S—CH2—, —C(O)—, or —O—; and
Y is phenyl, pyridyl, naphthyl, pyridone, pyrazine, benzodixane, benzopyridine, pyrimidine or benzothiazole, each optionally substituted by
C1-10-alkyl, C1-10-alkoxy, halogen or NO2 or, where Y is phenyl, by
or a pharmaceutically acceptable salt thereof,
with the provisos that
(a) if R3 and R6 are both H, one of R4 or R5 is not H,
(c) R6 is phenyl substituted by halogen, alkoxy substituted by hydroxy, —SO2CF2H, —OR1CONHR1,
furyloxy or —N(SO2R1)2; or R6′ is
(c) the compounds have a pKa greater than 10.
15. A compound according to claim 14, wherein
R3 is H, halogen or C1-10-alkyl optionally substituted by halogen, up to perhalo, NO2, —SO2F or —SO2CF3;
R4 is H, C1-10-alkyl, C1-10-alkoxy, halogen or NO2;
R5 is H, C1-10-alkyl optionally substituted by halogen, up to perhalo;
R6 is H, hydroxy, C1-10-alkoxy optionally substituted by at least one hydroxy group;
—COOR1; —OR1CONHR1; —NHCOR1; —SR1; phenyl optionally substituted by halo
or C1-10-alkoxy; NH2; —N(SO2R1)2, furyloxy,
16. A compound according to claim 14, wherein R3 is Cl, F, C4-5-branched alkyl, —SO2F or —SO2CF3; and R6 is hydroxy; C1-10-alkoxy optionally substituted by at least one hydroxy group; —COOR1; —OR1CONHR1; —NHCOR1; —SR1; phenyl optionally substituted by halo or C1-10-alkoxy; NH2; —N(SO2R1)2, furyloxy,
17. A compound according to claim 14, wherein R4′ is C1-10-alkyl or halogen; R5′ is H, C1-10-alkyl, halogen, CF3, halogen, NO2 or NH2; and R6′ is H, C1-10-alkyl, halogen, —NHCOCH3, —N(CH3)COCH3, NO2,
18. A compound according to claim 14, wherein R3 is t-butyl or CF3 and R6 is —OCH3.
19. A compound according to claim 14, which is
N-(5-tert-Butyl-2-(N-methylaminocarbonyl)methoxyphenyl)-N′-(2,3-dichlorophenyl)urea;
N-(5-tert-Butyl-2-(N-methylaminocarbonyl)methoxyphenyl)-N′-(1-naphthyl)urea;
N-(5-tert-Butyl-2-(N-morpholinocarbonyl)methoxyphenyl)-N′-(2,3-dichlorophenyl)urea;
N-(5-tert-Butyl-2-(N-morpholinocarbonyl)methoxyphenyl)-N′-(1-naphthyl)urea;
N-(5-tert-Butyl-2-(3-tetrahydrofuranyloxy)phenyl)-N′-(2,3-dichlorophenyl)urea;
N-(5-Difluoromethanesulfonyl)-2-methoxyphenyl)-N′-(4-methylphenyl)urea;
N-(5-(Difluoromethanesulfonyl)-2-methoxyphenyl)-N′-(4-fluorophenyl)urea;
N-(5-(Difluoromethanesulfonyl)-2-methoxyphenyl)-N′-(4-methyl-2-fluorophenyl)urea;
N-(5-(Difluoromethanesulfonyl)-2-methoxyphenyl)-N′-(4-methyl-3-fluorophenyl)urea;
N-(5-(Difluoromethanesulfonyl)-2-methoxyphenyl)-N′-(4-methyl-3-chlorophenyl)urea;
N-(5-(Difluoromethanesulfonyl)-2-methoxyphenyl)-N′-4-fluoro-3-chlorophenyl)urea;
N-(5-(Difluoromethanesulfonyl)-2-methoxyphenyl)-N′-(4-fluoro-3-methylphenyl)urea;
N-(5-(Difluoromethanesulfonyl)-2-methoxyphenyl)-N′-(2,3-dimethylphenyl)urea; or
N-(5-(Trifluoromethanesulfonyl)-2-methoxphenyl)-N′-(4-methylphenyl)urea.
20. A compound of formula II
wherein
R3, R4, R5, and R6 are each independently H; halogen; C1-10-alkyl optionally substituted by halogen up to perhalo; C1-10-alkoxy optionally substituted by at least one hydroxy group; NO2; SO2F; —SO2CHnX3-n; —COOR1; —OR1CONHR1; —NHCOR1; —SR1; phenyl optionally substituted by halogen or C1-10-alkoxy; NH2; —N(SO2R1)2; furyloxy;
2 adjacent R3-R6 can together form an aryl or hetaryl ring with 5-12 atoms, optionally substituted by C1-10-alkyl, C1-10-alkoxy, C3-10-cycloalkyl, C2-10-alkenyl, C1-10-alkanoyl, C6-12-aryl, C5-12-hetaryl, C6-12-aralkyl, C6-12-alkaryl, halogen; —NR1; —NO2; —CF3; —COOR1; —NHCOR1; —CN; —CONR1R1; —SO2R2; —SOR2; —SR2; in which R1 is H or C1-10-alkyl and R2 is C1-10-alkyl;
R3′, R4′ and R5′ are each independently H, C1-10-alkyl optionally substituted by halogen, up to perhalo; halogen; NO2 or NH2;
R6′ is H, C1-10-alkyl, halogen, —NHCOR1; —NR1COR1; NO2;
R1 is C1-10-alkyl;
n is 0 or 1;
X is —CH2—, —S— or —O—; and
Y is phenyl, pyridyl, naphthyl or benzothiazole, each optionally substituted by C1-10-alkyl, C1-10-alkoxy, halogen or NO2 or, where Y is phenyl, by
or a pharmaceutically acceptable salt thereof
with the provisos that
(a) if R3 and R6 are both H, one of R4 or R5 is not H, and
(b) R6 is alkoxy substituted by hydroxy, —SO2CF2H, —OR1CONHR1,
furyloxy or —N(SO2R1)2; or R6 is
21. A pharmaceutical composition comprising a compound of claim 14, and a physiologically acceptable carrier.
22. A pharmaceutical composition comprising a compound of claim 20, and a physiologically acceptable carrier.
Description
  • [0001]
    This application is a continuation of U.S. Ser. No. 10/060,396, filed Feb. 1, 2002, which is a continuation of U.S. Ser. No. 09/458,015, filed Dec. 10, 1999 (now abandoned), which is a Continuation in Part of U.S. Ser. No. 09/285,522, filed Dec. 22, 1998 (now abandoned), which claimed priority of Provisional Application 60/126,439, filed Dec. 22, 1997, all of which are incorporated by reference herein.
  • FIELD OF THE INVENTION
  • [0002]
    This invention relates to the use of a group of aryl ureas in treating cytokine mediated diseases and proteolytic enzyme mediated diseases, and pharmaceutical compositions for use in such therapy.
  • BACKGROUND OF THE INVENTION
  • [0003]
    Two classes of effector molecules which are critical for the progression of rheumatoid arthritis are pro-inflammatory cytokines and tissue degrading proteases. Recently, a family of kinases was described which is instrumental in controlling the transcription and translation of the structural genes coding for these effector molecules.
  • [0004]
    The mitogen-activated protein (MAP) kinase family is made up of a series of structurally related proline-directed serine/threonine kinases which are activated either by growth factors (such as EGF) and phorbol esters (ERK), or by IL-1, TNFα or stress (p38, JNK). The MAP kinases are responsible for the activation of a wide variety of transcription factors and proteins involved in transcriptional control of cytokine production. A pair of novel protein kinases involved in the regulation of cytokine synthesis was recently described by a group from SmithKline Beecham (Lee et al. Nature 1994, 372, 739). These enzymes were isolated based on their affinity to bond to a class of compounds, named CSAIDSs (cytokine suppressive anti-inflammatory drugs) by SKB. The CSAIDs, bicyclic pyridinyl imidazoles, have been shown to have cytokine inhibitory activity both in vitro and in vivo. The isolated enzymes, CSBP-1 and -2 (CSAID binding protein 1 and 2) have been cloned and expressed. A murine homologue for CSBP-2, p38, has also been reported (Han et al. Science 1994, 265, 808).
  • [0005]
    Early studies suggested that CSAIDs function by interfering with m-RNA translational events during cytokine biosynthesis. Inhibition of p38 has been shown to inhibit both cytokine production (eg., TNFα, IL-1, IL-6, IL-8) and proteolytic enzyme production (eg., MMP-1, MMP-3) in vitro and/or in vivo.
  • [0006]
    Clinical studies have linked TNFα production and/or signaling to a number of diseases including rheumatoid arthritis (Maini. J. Royal Coil. Physicians London 1996, 30, 344). In addition, excessive levels of TNFα have been implicated in a wide variety of inflammatory and/or immunomodulatory diseases, including acute rheumatic fever (Yegin et al. Lancet 1997, 349, 170), bone resorption (Pacifici et al. J. Clin. Endocrinol. Metabol. 1997, 82, 29), postmenopausal osteoperosis (Pacifici et al. J. Bone Mineral Res. 1996, 11, 1043), sepsis (Blackwell et al. Br. J. Anaesth. 1996, 77, 110), gram negative sepsis (Debets et al. Prog. Clin. Biol. Res. 1989, 308, 463), septic shock (Tracey et al. Nature 1987, 330, 662; Girardin et al. New England J. Med. 1988, 319, 397), endotoxic shock (Beutler et al. Science 1985, 229, 869; Ashkenasi et al. Proc. Nat'l. Acad. Sci. USA 1991, 88, 10535), toxic shock syndrome, (Saha et al. J. Immunol. 1996, 157, 3869; Lina et al. FEMS Immunol. Med. Microbiol. 1996, 13, 81), systemic inflammatory response syndrome (Anon. Crit. Care Med. 1992, 20, 864), inflammatory bowel diseases (Stokkers et al. J. Inflamm. 1995-6, 47, 97) including Crohn's disease (van Deventer et al. Aliment. Pharmacol. Therapeu. 1996, 10 (Suppl. 2), 107; van Dullemen et al. Gastroenterology 1995, 109, 129) and ulcerative colitis (Masuda et al. J. Clin. Lab. Immunol. 1995, 46, 111), Jarisch-Herxheimer reactions (Fekade et al. New England J. Med. 1996, 335, 311), asthma (Amrani et al. Rev. Malad. Respir. 1996, 13, 539), adult respiratory distress syndrome (Roten et al. Am. Rev. Respir. Dis. 1991, 143, 590; Suter et al. Am. Rev. Respir. Dis. 1992, 145, 1016), acute pulmonary fibrotic diseases (Pan et al. Pathol. Int. 1996, 46, 91), pulmonary sarcoidosis (Ishioka et al. Sarcoidosis Vasculitis Diffuse Lung Dis. 1996, 13, 139), allergic respiratory diseases (Casale et al. Am. J. Respir. Cell Mol. Biol. 1996, 15, 35), silicosis (Gossart et al. J. Immunol. 1996, 156, 1540; Vanhee et al. Eur. Respir. J. 1995, 8, 834), coal worker's pneumoconiosis (Borm et al. Am. Rev. Respir. Dis. 1988, 138, 1589), alveolar injury (Horinouchi et al. Am. J. Respir. Cell Mol. Biol. 1996, 14, 1044), hepatic failure (Gantner et al. J. Pharmacol. Exp. Therap. 1997, 280, 53), liver disease during acute inflammation (Kim et al. J. Biol. Chem. 1997, 272, 1402), severe alcoholic hepatitis (Bird et al. Ann. Intern. Med. 1990, 112, 917), malaria (Grau et al. Immunol. Rev. 1989, 112, 49; Taverne et al. Parasitol. Today 1996, 12, 290) including Plasmodium falciparum malaria (Perlmann et al. Infect. Immunit. 1997, 65, 116) and cerebral malaria (Rudin et al. Am. J. Pathol. 1997, 150, 257), non-insulin-dependent diabetes mellitus (NIDDM; Stephens et al. J. Biol. Chem. 1997, 272, 971; Ofei et al. Diabetes 1996, 45, 881), congestive heart failure (Doyama et al. Int. J. Cardiol. 1996, 54, 217; McMurray et al. Br. Heart J. 1991, 66, 356), damage following heart disease (Malkiel et al. Mol. Med. Today 1996, 2, 336), atherosclerosis (Parums et al. J. Pathol. 1996, 179, A46), Alzheimer's disease (Fagarasan et al. Brain Res. 1996, 723, 231; Aisen et al. Gerontology 1997, 43, 143), acute encephalitis (Ichiyama et al. J. Neurol. 1996, 243, 457), brain injury (Cannon et al. Crit. Care Med. 1992, 20, 1414; Hansbrough et al. Surg. Clin. N. Am. 1987, 67, 69; Marano et al. Surg. Gynecol. Obstetr. 1990, 170, 32), multiple sclerosis (M. S.; Coyle. Adv. Neuroimmunol. 1996, 6, 143; Matusevicius et al. J. Neuroimmunol. 1996, 66, 115) including demyelation and oligiodendrocyte loss in multiple sclerosis (Brosnan et al. Brain Pathol. 1996, 6, 243), advanced cancer (MucWierzgon et al. J. Biol. Regulators Homeostatic Agents 1996, 10, 25), lymphoid malignancies (Levy et al. Crit. Rev. Immunol. 1996, 16, 31), pancreatitis (Exley et al. Gut 1992, 33, 1126) including systemic complications in acute pancreatitis (McKay et al. Br. J. Surg. 1996, 83, 919), impaired wound healing in infection inflammation and cancer (Buck et al. Am. J. Pathol. 1996, 149, 195), myelodysplastic syndromes (Raza et al. Int. J. Hematol. 1996, 63, 265), systemic lupus erythematosus (Maury et al. Arthritis Rheum. 1989, 32, 146), biliary cirrhosis (Miller et al. Am. J. Gasteroenterolog. 1992, 87, 465), bowel necrosis (Sun et al. J. Clin. Invest. 1988, 81, 1328), psoriasis (Christophers. Austr. J. Dermatol. 1996, 37, 54), radiation injury (Redlich et al. J. Immunol. 1996, 157, 1705), and toxicity following administration of monoclonal antibodies such as OKT3 (Brod et al. Neurology 1996, 46, 1633). TNFα levels have also been related to host-versus-graft reactions (Piguet et al. Immunol. Ser. 1992, 56, 409) including ischemia reperfusion injury (Colletti et al. J. Clin. Invest. 1989, 85, 1333) and allograft rejections including those of the kidney (Maury et al. J. Exp. Med. 1987, 166, 1132), liver (Imagawa et al. Transplantation 1990, 50, 219), heart (Bolling et al. Transplantation 1992, 53, 283), and skin (Stevens et al. Transplant. Proc. 1990, 22, 1924), lung allograft rejection (Grossman et al. Immunol. Allergy Clin. N. Am. 1989, 9, 153) including chronic lung allograft rejection (obliterative bronchitis; LoCicero et al. J. Thorac. Cardiovasc. Surg. 1990, 99, 1059), as well as complications due to total hip replacement (Cirino et al. Life Sci. 1996, 59, 86). TNFα has also been linked to infectious diseases (review: Beutler et al. Crit. Care Med. 1993, 21, 5423; Degre. Biotherapy 1996, 8, 219) including tuberculosis (Rook et al. Med. Malad. Infect. 1996, 26, 904), Helicobacter pylori infection during peptic ulcer disease (Beales et al. Gastroenterology 1997, 112, 136), Chaga's disease resulting from Trypanosoma cruzi infection (Chandrasekar et al. Biochem. Biophys. Res. Commun. 1996, 223, 365), effects of Shiga-like toxin resulting from E. coli infection (Harel et al. J. Clin. Invest. 1992, 56, 40), the effects of enterotoxin A resulting from Staphylococcus infection (Fischer et al. J. Immunol. 1990, 144, 4663), meningococcal infection (Waage et al. Lancet 1987, 355; Ossege et al. J. Neurolog. Sci. 1996, 144, 1), and infections from Borrelia burgdorferi (Brandt et al. Infect. Immunol. 1990, 58, 983), Treponema pallidum (Chamberlin et al. Infect. Immunol. 1989, 57, 2872), cytomegalovirus (CMV; Geist et al. Am. J. Respir. Cell Mol. Biol. 1997, 16, 31), influenza virus (Beutler et al. Clin. Res. 1986, 34, 491a), Sendai virus (Goldfield et al. Proc. Nat'l. Acad. Sci. USA 1989, 87, 1490), Theiler's encephalomyelitis virus (Sierra et al. Immunology 1993, 78, 399), and the human immunodeficiency virus (HIV; Poli. Proc. Nat'l. Acad. Sci. USA 1990, 87, 782; Vyakaram et al. AIDS 1990, 4, 21; Badley et al. J. Exp. Med. 1997, 185, 55).
  • [0007]
    Because inhibition of p38 leads to inhibition of TNFα production, p38 inhibitors will be useful in treatment of the above listed diseases.
  • [0008]
    A number of diseases are thought to be mediated by excess or undesired matrix-destroying metalloprotease (MM) activity or by an imbalance in the ratio of the MMPs to the tissue inhibitors of metalloproteinases (TIMPs). These include osteoarthritis (Woessner et al. J. Biol. Chem. 1984, 259, 3633), rheumatoid arthritis (Mullins et al. Biochim. Biophys. Acta 1983, 695, 117; Woolley et al. Arthritis Rheum. 1977, 20, 1231; Gravallese et al. Arthritis Rheum. 1991, 34, 1076), septic arthritis (Williams et al. Arthritis Rheum. 1990, 33, 533), tumor metastasis (Reich et al. Cancer Res. 1988, 48, 3307; Matrisian et al. Proc. Nat'l. Acad. Sci., USA 1986, 83, 9413), periodontal diseases (Overall et al. J. Periodontal Res. 1987, 22, 81), corneal ulceration (Burns et al. Invest. Opthalmol. Vis. Sci. 1989, 30, 1569), proteinuria (Baricos et al. Biochem. J. 1988, 254, 609), coronary thrombosis from atherosclerotic plaque rupture (Henney et al. Proc. Nat'l. Acad. Sci., USA 1991, 88, 8154), aneurysmal aortic disease (Vine et al. Clin. Sci. 1991, 81, 233), birth control (Woessner et al. Steroids 1989, 54, 491), dystrophobic epidermolysis bullosa (Kronberger et al. J. Invest. Dermatol. 1982, 79, 208), degenerative cartilage loss following traumatic joint injury, osteopenias mediated by MMP activity, tempero mandibular joint disease, and demyelating diseases of the nervous system (Chantry et al. J. Neurochem. 1988, 50, 688).
  • [0009]
    Because inhibition of p38 leads to inhibition of MMP production, p38 inhibitors will be useful in treatment of the above listed diseases.
  • [0010]
    Inhibitors of p38 are active in animal models of TNFα production, including a murine lipopolysaccharide (LPS) model of TNFα production. Inhibitors of p38 are active in a number of standard animal models of inflammatory diseases, including carrageenan-induced edema in the rat paw, arachadonic acid-induced edema in the rat paw, arachadonic acid-induced peritonitis in the mouse, fetal rat long bone resorption, murine type II collagen-induced arthritis, and Fruend's adjuvant-induced arthritis in the rat. Thus, inhibitors of p38 will be useful in treating diseases mediated by one or more of the above-mentioned cytokines and/or proteolytic enzymes.
  • [0011]
    The need for new therapies is especially important in the case of arthritic diseases. The primary disabling effect of osteoarthritis, rheumatoid arthritis and septic arthritis is the progressive loss of articular cartilage and thereby normal joint function. No marketed pharmaceutical agent is able to prevent or slow this cartilage loss, although nonsteroidal antiinflammatory drugs (NSAIDs) have been given to control pain and swelling. The end result of these diseases is total loss of joint function which is only treatable by joint replacement surgery. P38 inhibitors will halt or reverse the progression of cartilage loss and obviate or delay surgical intervention.
  • [0012]
    Several patents have appeared claiming polyarylimidazoles and/or compounds containing polyarylimidazoles as inhibitors of p38 (for example, Lee et al. WO 95/07922; Adams et al. WO 95/02591; Adams et al. WO 95/13067; Adams et al. WO 95/31451). It has been reported that arylimidazoles complex to the ferric form of cytochrome P450cam (Harris et al. Mol. Eng. 1995, 5, 143, and references therein), causing concern that these compounds may display structure-related toxicity (Howard-Martin et al. Toxicol. Pathol. 1987, 15, 369). Therefore, there remains a need for improved p38 inhibitors.
  • SUMMARY OF THE INVENTION
  • [0013]
    This invention provides compounds, generally described as aryl ureas, including both aryl and heteroaryl analogues, which inhibit p38 mediated events and thus inhibit the production of cytokines (such as TNFα, IL-1 and IL-8) and proteolytic enzymes (such as MMP-1 and MMP-3). The invention also provides a method of treating a cytokine mediated disease state in humans or mammals, wherein the cytokine is one whose production is affected by p38. Examples of such cytokines include, but are not limited to TNFα, IL-1 and IL-8. The invention also provides a method of treating a protease mediated disease state in humans or mammals, wherein the protease is one whose production is affected by p38. Examples of such proteases include, but are not limited to collagenase (MMP-1) and stromelysin (MMP-3).
  • [0014]
    Accordingly, these compounds are useful therapeutic agents for such acute and chronic inflammatory and/or immunomodulatory diseases as rheumatoid arthritis, osteoarthritis, septic arthritis, rheumatic fever, bone resorption, postmenopausal osteoperosis, sepsis, grain negative sepsis, septic shock, endotoxic shock, toxic shock syndrome, systemic inflammatory response syndrome, inflammatory bowel diseases including Crohn's disease and ulcerative colitis, Jarisch-Herxheimer reactions, asthma, adult respiratory distress syndrome, acute pulmonary fibrotic diseases, pulmonary sarcoidosis, allergic respiratory diseases, silicosis, coal worker's pneumoconiosis, alveolar injury, hepatic failure, liver disease during acute inflammation, severe alcoholic hepatitis, malaria including Plasmodium falciparum malaria and cerebral malaria, non-insulin-dependent diabetes mellitus (NIDDM), congestive heart failure, damage following heart disease, atherosclerosis, Alzheimer's disease, acute encephalitis, brain injury, multiple sclerosis including demyelation and oligiodendrocyte loss in multiple sclerosis, advanced cancer, lymphoid malignancies, tumor metastasis, pancreatitis, including systemic complications in acute pancreatitis, impaired wound healing in infection, inflammation and cancer, periodontal diseases, corneal ulceration, proteinuria, myelodysplastic syndromes, systemic lupus erythematosus, biliary cirrhosis, bowel necrosis, psoriasis, radiation injury, toxicity following administration of monoclonal antibodies such as OKT3, host-versus-graft reactions including ischemia reperfusion injury and allograft rejections including kidney, liver, heart, and skin allograft rejections, lung allogaft rejection including chronic lung allograft rejection (obliterative bronchitis) as well as complications due to total hip replacement, and infectious diseases including tuberculosis, Helicobacter pylori infection during peptic ulcer disease, Chaga's disease resulting from Trypanosoma cruzi infection, effects of Shiga-like toxin resulting from E. coli infection, effects of enterotoxin A resulting from Staphylococcus infection, meningococcal infection, and infections from Borrelia burgdorferi, Treponema pallidum, cytomegalovirus, influenza virus, Theiler's encephalomyelitis virus, and the human immunodeficiency virus (HIV).
  • [0015]
    The present invention, therefore, provides compounds generally described as aryl ureas, including both aryl and heteroaryl analogues, which inhibit the p38 pathway. The invention also provides a method for treatment of p38-mediated disease states in humans or mammals, e.g., disease states mediated by one or more cytokines or proteolytic enzymes produced and/or activated by a p38 mediated process. Thus, the invention is directed to compounds and methods for the treatment of diseases mediated by p38 kinase comprising administering a compound of Formula I
  • [0000]
  • [0000]
    wherein
      • A is
  • [0000]
  • [0017]
    B is a substituted or unsubstituted, up to tricyclic aryl or heteroaryl moiety of up to 30 carbon atoms with at least one 6-member aromatic structure containing 0-4 members of the group consisting of nitrogen, oxygen and sulfur, wherein if B is substituted, it is substituted by one or more substituents selected from the group consisting of halogen, up to per-halo, and Wn, wherein n is 0-3 and each W is independently selected from the group consisting of —CN, —CO2R7, —C(O)NR7R7, —C(O)—R7, —NO2, —OR7, —SR7, —NR7R7, —NR7C(O)OR7, —NR7C(O)R7, C1-C10 alkyl, C2-10-alkenyl, C1-10-alkoxy, C3-C10 cycloalkyl, C6-C14 aryl, C7-C24 alkaryl, C3-C13 heteroaryl, C4-C23 alkheteroaryl, substituted C1-C10 alkyl, substituted C2-10-alkenyl, substituted C1-10-alkoxy, substituted C3-C10 cycloalkyl, substituted C4-C23 alkheteroaryl and Q-Ar;
      • wherein if W is a substituted group, it is substituted by one or more substituents independently selected from the group consisting of —CN, —CO2R7, —C(O)R7, —C(O)NR7R7, —OR7, —SR7, —NR7R7, NO2, —NR7C(O)R7, —NR7C(O)OR7 and halogen up to per-halo;
      • wherein each R7 is independently selected from H, C1-C10 alkyl, C2-10-alkenyl, C3-C10 cycloalkyl, C6-C14 aryl, C3-C13 hetaryl, C7-C24 alkaryl, C4-C23 alkheteroaryl, up to per-halosubstituted C1-C10 alkyl, up to per-halosubstituted C2-10-alkenyl, up to per-halosubstituted C3-C10 cycloalkyl, up to per-halosubstituted C6-C14 aryl and up to per-halosubstituted C3-C13 hetaryl,
      • wherein Q is —O—, —S—, —N(R7)—, —(CH2)—m, —C(O)—, —CH(OH)—, —(CH2)mO—, —NR7C(O)NR7R7′—, —NR7C(O)—, —C(O)NR7, —(CH2)mS—, —(CH2)mN(R7)—, —O(CH2)m—, —CHXa, —CXa 2, —S—(CH2)m— and —N(R7)(CH2)m—,
      • m=1-3, and Xa is halogen; and
  • [0022]
    Ar is a 5-10 member aromatic structure containing 0-2 members of the group consisting of nitrogen, oxygen and sulfur, which is unsubstituted or substituted by halogen up to per-halo and optionally substituted by Zn1 wherein n1 is 0 to 3 and each Z is independently selected from the group consisting of —CN, —CO2R7, —C(O)NR7R7, —C(O)—NR7, —C(O)R7, —NO2, —OR7, —SR7, —NR7R7, —NR7C(O)OR7, —NR7C(O)R7, C1-C10 alkyl, C3-C10 cycloalkyl, C6-C14 aryl, C3-C13 hetaryl, C7-C24 alkaryl, C4-C23 alkheteroaryl, substituted C1-C10 alkyl, substituted C3-C10 cycloalkyl, substituted C7-C24 alkaryl and substituted C4-C23 alkheteroaryl; wherein the one or more substituents of Z is selected from the group consisting of —CN, —CO2R7, —C(O)NR7R7, —OR7, —SR7, —NO2, —NR7R7, —NR7C(O)R7, —NR7C(O)OR7,
    • R3′, R4′, R5′ are each independently H, C1-10-alkyl, optionally substituted by halogen, up to perhalo, C1-10 alkoxy, optionally substituted by halogen, up to perhaloalkoxy, halogen; NO2 or NH2;
    • R6 is H, C1-10-alkyl, C1-10 alkoxy, —NHCOR1; —NR1COR1; NO2;
  • [0000]
      • one of R4′, R5′ or R6′ can be —X—Y,
      • or 2 adjacent R4′-R6′ can together be an aryl or hetaryl ring with 5-12 atoms, optionally substituted by C1-10-alkyl, C1-10 alkoxy, C3-10 cycloalkyl, C2-10 alkenyl C1-10 alkanoyl, C6-12 aryl, C5-12 hetaryl or C6-12 aralkyl;
    • R1 is C1-10-alkyl optionally substituted by halogen, up to perhalo;
    • X is —CH2—, —S—, —N(CH3)—, —NHC(O)—, —CH2—S—, —S—CH2—, —C(O)—, or —O—; and
    • X is additionally a single bond where Y is pyridyl;
    • Y is phenyl, pyridyl, naphthyl, pyridone, pyrazine, benzodioxane, benzopyridine, pyrimidine or benzothiazole, each optionally substituted by C1-10-alkyl, C1-10-alkoxy, halogen, OH, —SCH3 or NO2 or, where Y is phenyl, by
  • [0000]
  • [0000]
    or a pharmaceutically acceptable salt thereof.
  • [0031]
    Preferably, the compounds of formula I are of formula Ia
  • [0000]
  • [0000]
    wherein
  • [0032]
    R3, R4, R5 and R6 are each independently H, halogen, C1-10-alkyl optionally substituted by halogen, up to perhalo, C1-10-alkoxy, optionally substituted by at least one hydroxy group or by halogen, up to perhalo; C6-12 aryl, optionally substituted by C1-10 alkoxy or halogen, C5-12 hetaryl, optionally substitued by C1-10 alkyl C1-10 alkoxy or halogen; NO2, SO2F or —SO2CHpX3-p; —COOR1; —OR1CONHR1; —NHCOR1; —SR1; phenyl optionally substituted by halo or C1-10-alkoxy; NH2; —N(SO2R1)2, furyloxy,
  • [0000]
      • 2 adjacent R3-R6 can together form an aryl or hetaryl ring with 5-12 atoms, optionally substituted by C1-10-alkyl, C1-10-alkoxy, C3-10-cycloalkyl, C2-10-alkenyl, C1-10-alkanoyl, C6-12-aryl, C5-12-hetaryl, C6-12-aralkyl, C6-12-alkaryl, halogen; —NR1; —NO2; —CF3; —COOR1; —NHCOR1; —CN; —CONR1R1; —SO2R2; —SOR2; —SR2; in which R1 is H or C1-10-alkyl and R2 is C1-10-alkyl; optionally substituted by halogen, up to perhalo, with —SO2-optionally incorporated in the aryl or hetaryl ring;
  • [0034]
    one of R4, R5 or R6 can be —X—Y,
    • R1 is C1-10-alkyl, optionally substituted by halogen, up to perhalo;
    • p is 0 or 1;
    • X is —CH2, —S—, N(CH3)—, —NHC(O), CH2—S—, —S—CH2—, —C(O)—, or —O—; and
    • Y is phenyl, pyridyl, naphthyl, pyridone, pyrazine, benzodixane, benzopyridine pyrimidine or benzothiazole, each optionally substituted by C1-10-alkyl, C1-10-alkoxy, halogen or NO2 or, where Y is phenyl, by
  • [0000]
  • [0000]
    with the proviso that if R3 and R6 are both H, one of R4 or R5 is not H.
  • [0039]
    In formula I, suitable hetaryl groups B include, but are not limited to, 5-12 carbon-atom aromatic rings or ring systems containing 1-3 rings, at least one of which is aromatic, in which one or more, e.g., 1-4 carbon atoms in one or more of the rings can be replaced by oxygen, nitrogen or sulfur atoms. Each ring typically has 3-7 atoms. For example, B can be 2- or 3-furyl, 2- or 3-thienyl, 2- or 4-triazinyl, 1-, 2- or 3-pyrrolyl, 1-, 2-, 4- or 5-imidazolyl, 1-, 3-, 4- or 5-pyrazolyl, 2-, 4- or 5-oxazolyl, 3-, 4- or 5-isoxazolyl, 2-, 4- or 5-thiazolyl, 3-, 4- or 5-isothiazolyl, 2-, 3- or 4-pyridyl, 2-, 4-, 5- or 6-pyrimidinyl, 1,2,3-triazol-1-, -4- or 5-yl, 1,2,4-triazol-1-, -3- or -5-yl, 1- or 5-tetrazolyl, 1,2,3-oxadiazol-4- or -5-yl, 1,2,4-oxadiazol-3- or -5-yl, 1,3,4-thiadiazol-2- or -5-yl, 1,2,4-oxadiazol-3- or -5-yl, 1,3,4-thiadiazol-2- or -5-yl, 1,3,4-thiadiazol-3- or -5-yl, 1,2,3-thiadiazol-4- or -5-yl, 2-, 3-, 4-, 5- or 6-2H-thiopyranyl, 2-, 3- or 4-4H-thiopyranyl, 3- or 4-pyridazinyl, pyrazinyl, 2-, 3-, 4-, 5-, 6- or 7-benzofuryl, 2-, 3-, 4-, 5-, 6- or 7-benzothienyl, 1-, 2-, 3-, 4-, 5-, 6- or 7-indolyl, 1-, 2-, 4- or 5-benzimidazolyl, 1-, 3-, 4-, 5-, 6- or 7-benzopyrazolyl, 2-, 4-, 5-, 6- or 7-benzoxazolyl, 3-, 4-, 5-6- or 7-benzisoxazolyl, 1-, 3-, 4-, 5-, 6- or 7-benzothiazolyl, 2-, 4-, 5-, 6- or 7-benzisothiazolyl, 2-, 4-, 5-, 6- or 7-benz-1,3-oxadiazolyl, 2-, 3-, 4-, 5-, 6-, 7- or 8-quinolinyl, 1-, 3-, 4-, 5-, 6-, 7-, 8-isoquinolinyl, 1-, 2-, 3-, 4- or 9-carbazolyl, 1-, 2-, 3-, 4-, 5-, 6-, 7-, 8- or 9-acridinyl, or 2-, 4-, 5-, 6-, 7- or 8-quinazolinyl, or additionally optionally substituted phenyl, 2- or 3-thienyl, 1,3,4-thiadiazolyl, 3-pyrryl, 3-pyrazolyl, 2-thiazolyl or 5-thiazolyl, etc. For example, B can be 4-methyl-phenyl, 5-methyl-2-thienyl, 4-methyl-2-thienyl, 1-methyl-3-pyrryl, 1-methyl-3-pyrazolyl, 5-methyl-2-thiazolyl or 5-methyl-1,2,4-thiadiazol-2-yl.
  • [0040]
    Suitable alkyl groups and alkyl portions of groups, e.g., alkoxy, etc. throughout include methyl, ethyl, propyl, butyl, etc., including all straight-chain and branched isomers such as isopropyl, isobutyl, sec-butyl, tert-butyl, etc.
  • [0041]
    Suitable aryl groups include, for example, phenyl and 1- and 2-naphthyl.
  • [0042]
    The term “cycloalkyl”, as used herein, refers to cyclic structures with or without alkyl substitutents such that, for example, “C4 cycloakyl” includes methyl substituted cyclopropyl groups as well as cyclobutyl groups. The term “cycloalkyl” also includes saturated heterocyclic groups.
  • [0043]
    Suitable halogen groups include F, Cl, Br, and/or I, from one to per-substitution (i.e. all H atoms on a group replaced by a halogen atom) being possible where an alkyl group is substituted by halogen, mixed substitution of halogen atom types also being possible on a given moiety.
  • [0044]
    Preferred compounds of formula I include those where R3 is H, halogen or C1-10-alkyl, optionally substituted by halogen, up to perhalo, NO2, —SO2F, —SO2CHF2; or —SO2CF3; R4 is H, C1-10-alkyl, C1-10-alkoxy, halogen or NO2; R5 is H, C1-10-alkyl optionally substituted by halogen, up to perhalo; R6 is H, hydroxy, C1-10-alkoxy, optionally substituted by at least one hydroxy group; —COOR1; —OR1CONHR1; —NHCOR1; —SR1; phenyl optionally substituted by halo or C1-10-alkoxy; NH2; —N(SO2R1)2, furyloxy,
      • Preferably, R3 is Cl, F, C4-5-branched alkyl, —SO2F or —SO2CF3; and R6 is hydroxy; C1-10-alkoxy optionally substituted by at least one hydroxy group; —COOR1; OR1CONHR1; —NHCOR1; —SR1; phenyl optionally substituted by halo or C1-10-alkoxy; NH2; —N(SO2R1)2, furyloxy,
  • [0046]
    More preferably, R6 is t-butyl or CF3 and R6 is —OCH3. Preferably, R4′ is C1-10-alkyl or halogen; R5′ is H, C1-10-alkyl, halogen, CF3, halogen, NO2 or NH2; and R6′ is H, C1-10-alkyl, halogen, —NHCOCH3, —N(CH3)COCH3, NO2,
  • [0000]
  • [0047]
    The invention also relates to compounds per se, of formula II
  • [0000]
  • [0000]
    wherein
  • [0048]
    R3, R4, R5 and R6 are each independently H, halogen, C1-10-alkyl optionally substituted by halogen up to perhalo, C1-10-alkoxy, optionally substituted by at least one hydroxy group or halogen, up to perhalo; NO2, SO2F or —SO2CHnX3-n, C1-10-alkoxy; —COOR1; —OR1CONHR1; —NHCOR1; —SR1; C6-12 aryl, optionally substituted by C1-10-alkyl, C1-10 alkoxy or halogen, C5-12 hetaryl, optionally substitued by C1-10 alkyl, C1-10 alkoxy or halogen; NH2; —N(SO2R1)2; furyloxy;
  • [0000]
      • 2 adjacent R3-R6 can together form an aryl or hetaryl ring with 5-12 atoms, optionally substituted by Cl1-10-alkyl, C1-10-alkoxy, C3-10-cycloakyl, C2-10-alkenyl, C1-10-alkanoyl, C6-12-aryl, C5-12-hetaryl, C6-12-aralkyl, C6-12-alkaryl, halogen; —NR1; —NO2; —CF3; —COOR1; —NHCOR1; —CN; —CONR1R1; —SO2R2; —SOR2; —SR2; in which R1 is H or C1-10-alkyl and R2 is C1-10-alkyl;
    • R3′, R4′ and R5′ are each independently H, C1-10-alkyl, optionally substituted by halogen, up to perhalo; NO2 or NH2;
    • R6 is H, C1-10-alkyl halogen, —NHCOR1; —NR1COR1; NO2;
  • [0000]
    • 2 adjacent R4′-R6′ can together be an aryl or hetaryl ring with 5-12 atoms;
    • R1 is C1-10-alkyl, optionally substituted by halogen, up to perhalo;
    • n is 0 or 1;
      with the provisos that
      • (a) if R3 and R6 are both H, one of R4 or R5 is not H, and
      • (b) that R6 is phenyl substituted by alkoxy or halogen, alkoxy substituted by hydroxy, —SO2CF2H, —OR1CONHR1,
  • [0000]
  • [0000]
    furyloxy or —N(SO2R1)2;
  • or R6′ is
  • [0057]
  • [0000]
    and (c) if R6 is phenyl substituted by alkoxy or halogen, the compounds have a pKa greater than 10, e.g., greater than 12, preferably greater than 15.
    Preferred 5-tert-butylphenyl ureas are:
    • N-(5-tert-Butyl-2-methoxyphenyl)-N′-(4-phenyloxphenyl)urea;
    • N-(5-tert-Butyl-2-methoxyphenyl)-N′-(4-(4-methoxyphenyloxy)phenyl)urea;
    • N-(5-tert-Butyl-2-methoxyphenyl)-N′-(4-(4-pyridinylmethyl)phenyl)urea;
    • N-(5-tert-Butyl-2-methoxyphenyl)-N′-(4-(4-pyridinylthio)phenyl)urea;
    • N-(5-tert-Butyl-2-methoxyphenyl)-N′-(4-(4-(4,7-methano-1H-isoindole-1,3(2H)-dionyl)methyl)phenyl)urea;
    • N-(5-tert-Butyl-2-phenylphenyl)-N′-(2,3-dichlorophenyl)urea;
    • N-(5-tert-Butyl-2-(3-thienyl)phenyl)-N′-(2,3-dichlorophenyl)urea;
    • N-(5-tert-Butyl-2-(N-methylaminocarbonyl)methoxyphenyl)-N′-(2,3-dichlorophenyl)urea;
    • N-(5-tert-Butyl-2-(N-methylaminocarbonyl)methoxyphenyl)-N′-(1-naphthyl)urea;
    • N-(5-tert-Butyl-2-(N-morpholinocarbonyl)methoxyphenyl)-N′-(2,3-dichlorophenyl)urea;
    • N-(5-tert-Butyl-2-(N-morpholinocarbonyl)methoxyphenyl)-N′-(1-naphthyl)urea;
    • N-(5-tert-Butyl-2-(3-tetrahydrofuranyloxy)phenyl)-N′-(2,3-dichlorophenyl)urea; and
    • N-(5-tert-Butyl-2-methoxyphenyl)-N′-(4-(3-pyridinyl)methylphenyl)urea.
      Preferred 5-trifluoromethylphenyl ureas are:
    • N-(5-Trifluoromethyl-2-methoxyphenyl)-N′-(4-methylphenyl)urea;
    • N-(5-Trifluoromethyl-2-methoxyphenyl)-N′-(4-methyl-2-fluorophenyl)urea;
    • N-(5-Trifluoromethyl-2-methoxyphenyl)-N′-(4-fluoro-3-chlorophenyl)urea;
    • N-(5-Trifluoromethyl-2-methoxyphenyl)-N′-(4-methyl-3-chlorophenyl)urea;
    • N-(5-Trifluoromethyl-2-methoxyphenyl)-N′-(4-methyl-3-fluorophenyl)urea;
    • N-(5-Trifluoromethyl-2-methoxyphenyl)-N′-(2,4-difluorophenyl)urea;
    • N-(5-Trifluoromethyl-2-methoxyphenyl)-N′-(4-phenyloxy-3,5-dichlorophenyl)urea;
    • N-(5-Trifluoromethyl-2-methoxyphenyl)-N′-(4-(4-pyridinylmethyl)phenyl)urea;
    • N-(5-Trifluoromethyl-2-methoxyphenyl)-N′-(4-(4-pyridinylthio)phenyl)urea;
    • N-(5-Trifluoromethyl-2-methoxyphenyl)-N′-(4-(4-pyridinyloxy)phenyl)urea;
    • N-(5-Trifluoromethyl-2-methoxyphenyl)-N′-(3-(4-pyridinylthio)phenyl)urea; and
    • N-(5-Trifluoromethyl-2-methoxyphenyl)-N′-(4-(3-(N-methylaminocarbonyl)-phenyloxy)phenyl)-urea.
      Preferred 5-sulfonylphenyl ureas are:
    • N-(5-Fluorosulfonyl)-2-methoxyphenyl)-N′-(4-methylphenyl)urea;
    • N-(5-(Difluoromethanesulfonyl)-2-methoxyphenyl)-N′-(4-methylphenyl)ureaN-(5-(Difluoromethanesulfonyl)-2-methoxyphenyl)-N′-(4-fluorophenyl)urea;
    • N-(5-(Difluoromethanesulfonyl)-2-methoxyphenyl)-N′-(4-methyl-2-fluorophenyl)urea;
    • N-(5-(Difluoromethanesulfonyl)-2-methoxyphenyl)-N′-(4-methyl-3-fluorophenyl)urea;
    • N-(5-(Difluoromethanesulfonyl)-2-methoxyphenyl)-N′-(4-methyl-3-chlorophenyl)urea;
    • N-(5-(Difluoromethanesulfonyl)-2-methoxyphenyl)-N′-(4-fluoro-3-chlorophenyl)urea;
    • N-(5-(Difluoromethanesulfonyl)-2-methoxyphenyl)-N′-(4-fluoro-3-methylphenyl)urea;
    • N-(5-(Difluoromethanesulfonyl)-2-methoxyphenyl)-N′-(2,3-dimethylphenyl)urea; and
    • N-(5-(Trifluoromethanesulfonyl)-2-methoxphenyl)-N′-(4-methylphenyl)urea.
      Preferred 2-naphthyl ureas are:
    • N-(3-Methoxy-2-naphthyl)-N′-(2-fluorophenyl)urea;
    • N-(3-Methoxy-2-naphthyl)-N′-(4-methylphenyl)urea;
    • N-(3-Methoxy-2-naphthyl)-N′-(3-fluorophenyl)urea;
    • N-(3-Methoxy-2-naphthyl)-N′-(4-methyl-3-fluorophenyl)urea;
    • N-(3-Methoxy-2-naphthyl)-N′-(2,3-dimethylphenyl)urea;
    • N-(3-Methoxy-2-naphthyl)-N′-(1-naphthyl)urea;
    • N-(3-Methoxy-2-naphthyl)-N′-(4-(4-pyridinylmethyl)phenyl)urea;
    • N-(3-Methoxy-2-naphthyl)-N′-(4-(4-pyridinylthio)phenyl)urea;
    • N-(3-Methoxy-2-naphthyl)-N′-(4-(4-methoxyphenyloxy)phenyl)urea; and
    • N-(3-Methoxy-2-naphthyl)-N′-(4-(4-(4,7-methano-1H-isoindole-1,3(2H)-dionyl)methyl)phenyl)urea.
      Other preferred ureas are:
    • N-(2-Hydroxy-4-nitro-5-chlorophenyl)-N′-(phenyl)urea; and
    • N-(2-Hydroxy-4-nitro-5-chlorophenyl)-N′-(4-(4-pyridinylmethly)phenyl)urea.
  • [0104]
    The present invention is also directed to pharmaceutically acceptable salts of formula I. Suitable pharmaceutically acceptable salts are well known to those skilled in the art and include basic salts of inorganic and organic acids, such as hydroebtoric acid, hydrobromic acid, sulphuric acid, phosphoric acid, methanesulphonic acid, sulphonic acid, acetic acid, trifluoroacetic acid, malic acid, tartaric acid, citric acid, lactic acid, oxalic acid, succinic acid, fumaric acid, maleic acid, benzoic acid, salicylic acid, phenylacetic acid, and mandelic acid. In addition, pharmaceutically acceptable salts include acid salts of inorganic bases, such as salts containing alkaline cations (e.g., Li+ Na+ or K+), alkaline earth cations (e.g., Mg+2, Ca+2 or Ba+2), the ammonium cation, as well as acid salts of organic bases, including aliphatic and aromatic substituted ammonium, and quaternary ammonium cations, such as those arising from protonation or peralkylation of triethylamine, N,N-diethylamine, N,N-dicyclohexylamine, pyridine, N,N-dimethylaminopyridine (DMAP), 1,4-diazabiclo[2.2.2]octane (DABCO), 1,5-diazabicyclo[4.3.0]non-5-ene (DBN) and 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU).
  • [0105]
    A number of the compounds of Formula I possess asymmetric carbons and can therefore exist in racemic and optically active forms. Methods of separation of enantiomeric and diastereomeric mixtures are well known to one skilled in the art. The present invention encompasses any isolated racemic or optically active form of compounds described in Formula I which possess p38 kinase inhibitory activity.
  • General Preparative Methods
  • [0106]
    The compounds of Formula I may be prepared by use of known chemical reactions and procedures, some from starting materials which are commercially available, Nevertheless, the following general preparative methods are presented to aid one of skill in the art in synthesizing these compounds, with more detailed particular examples being presented in the experimental section describing the working examples.
  • [0000]
  • [0107]
    Nitroaryls are commonly formed by electrophilic aromatic nitration using HNO3, or an alternative NO2 + source. Nitroaryls may be further elaborated prior to reduction. Thus, nitroaryls substituted with
  • [0000]
  • [0000]
    potential leaving groups (eg. F, Cl, Br, etc.) may undergo substitution reactions on treatment with nucleophiles, such as thiolate (exemplified in Scheme II) or phenoxide. Nitroaryls may also undergo Ullman-type coupling reactions (Scheme II).
  • [0000]
      • Nitroaryls may also undergo transition metal mediated cross coupling reactions. For example, nitroaryl electrophiles, such as nitroaryl bromides, iodides or triflates, undergo palladium mediated cross coupling reactions with aryl nucleophiles, such as arylboronic acids (Suzuki reactions, exemplified below), aryltins (Stille reactions) or arylzincs (Negishi reaction) to afford the biaryl (5).
  • [0000]
      • Either nitroaryls or anilines may be converted into the corresponding arenesulfonyl chloride (7) on treatment with chlorosulfonic acid. Reaction of the sualfonyl chloride with a fluoride source, such as KF then affords sulfonyl fluoride (8). Reaction of sulfonyl fluoride 8 with trimethylsilyl trifluoromethane in the presence of a fluoride source, such as tris(dimethylamino)sulfonium difluorotrimethylsiliconate (TASF) leads to the corresponding trifluoromethylsulfone (9). Alternatively, sulfonyl chloride 7 may be reduced to the arenethiol (10), for example with zinc amalgum. Reaction of thiol 10 with CHClF2 in the presence of base gives the difluoromethyl mercaptam (11), which may be oxidized to the sulfone (12) with any of a variety of oxidants, including CrO3-acetic anhydride (Sedova et al. Zh. Org. Khim. 1970, 6, 568).
  • [0000]
      • As shown in Scheme IV, non-symmetrical urea formation may involve reaction of an aryl isocyanate (14) with an aryl amine (13). The heteroaryl isocyanate may be synthesized from a heteroaryl amine by treatment with phosgene or a phosgene equivalent, such as trichloromethyl chloroformate (diphosgene), bis(trichloromethyl) carbonate (triphosgene), or NN′-carbonyldiimidazole (CDI). The isocyanate may also be derived from a heterocyclic carboxylic acid derivative, such as an ester, an acid halide or an anhydride by a Curtius-type rearrangement. Thus, reaction of acid derivative 16 with an azide source, followed by rearrangement affords the isocyanate. The corresponding carboxylic acid (17) may also be subjected to Curtius-type rearrangements using diphenylphosphoryl azide (DPPA) or a similar reagent.
  • [0000]
      • Finally, ureas may be further manipulated using methods familiar to those skilled in the art.
  • [0112]
    The invention also includes pharmaceutical compositions including a compound of Formula I, and a physiologically acceptable carrier.
  • [0113]
    The compounds may be administered orally, topically, parenterally, by inhalation or spray, vaginally, rectally or sublingually in dosage unit formulations. The term ‘administration by injection’ includes intravenous, intramuscular, subcutaneous and parenteral injections, as well as use of Infusion techniques. Dermal administration may include topical application or transdermal administration. One or more compounds may be present in association with one or more non-toxic pharmaceutically acceptable carriers and if desired other active ingredients.
  • [0114]
    Compositions intended for oral use may be prepared according to any suitable method known to the art for the manufacture of pharmaceutical compositions. Such compositions may contain one or more agents selected from the group consisting of diluents, sweetening agents, flavoring agents, coloring agents and preserving agents in order to provide palatable preparations. Tablets contain the active ingredient in admixture with non-toxic pharmaceutically acceptable excipients which are suitable for the manufacture of tablets. These excipients may be, for example, inert diluents, such as calcium carbonate, sodium carbonate, lactose, calcium phosphate or sodium phosphate; granulating and disintegrating agents, for example, corn starch, or alginic acid; and binding agents, for example magnesium stearate, stearic acid or talc. The tablets may be uncoated or they may be coated by known techniques to delay disintegration and adsorption in the gastrointestinal tract and thereby provide a sustained action over a longer period. For example, a time delay material such as glyceryl monostearate or glyceryl distearate may be employed. These compounds may also be prepared in solid, rapidly released form.
  • [0115]
    Formulations for oral use may also be presented as hard gelatin capsules wherein the active ingredient is mixed with an inert solid diluent, for example, calcium carbonate, calcium phosphate or kaolin, or as soft gelatin capsules wherein the active ingredient is mixed with water or an oil medium, for example peanut oil, liquid paraffin or olive oil.
  • [0116]
    Aqueous suspensions containing the active materials in admixture with excipients suitable for the manufacture of aqueous suspensions may also be used. Such excipients are suspending agents, for example sodium carboxymethylcellulose, methylcellulose, hydroxypropyl-methylcellulose, sodium alginate, polyvinylpyrrolidone, gum tragacanth and gum acacia; dispersing or wetting agents may be a naturally-occurring phosphatide, for example, lecithin, or condensation products of an alkylene oxide with fatty acids, for example polyoxyethylene stearate, or condensation products of ethylene oxide with long chain aliphatic alcohols, for example heptadecaethyleneoxycetanol, or condensation products of ethylene oxide with partial esters derived from fatty acids and hexitol such as polyoxyethylene sorbitol monooleate, or condensation products of ethylene oxide with partial esters derived from fatty acids and hexitol anhydrides, for example polyethylene sorbitan monooleate. The aqueous suspensions may also contain one or more preservatives, for example ethyl, or n-propyl, p-hydroxybenzoate, one or more coloring agents, one or more flavoring agents, and one or more sweetening agents, such as sucrose or saccharin.
  • [0117]
    Dispersible powders and granules suitable for preparation of an aqueous suspension by the addition of water provide the active ingredient in admixture with a dispersing or wetting agent, suspending agent and one or more preservatives. Suitable dispersing or wetting agents and suspending agents are exemplified by those already mentioned above. Additional excipients, for example, sweetening, flavoring and coloring agents, may also be present.
  • [0118]
    The compounds may also be in the form of non-aqueous liquid formulations, e.g., oily suspensions which may be formulated by suspending the active ingredients in a vegetable oil, for example arachis oil, olive oil, sesame oil or peanut oil, or in a mineral oil such as liquid paraffin. The oily suspensions may contain a thickening agent, for example beeswax, hard paraffin or cetyl alcohol. Sweetening agents such as those set forth above, and flavoring agents may be added to provide palatable oral preparations. These compositions may be preserved by the addition of an anti-oxidant such as ascorbic acid.
  • [0119]
    Compounds of the invention may also be administrated transdermally using methods known to those skilled in the art (see, for example: Chien; “Transdermal Controlled Systemic Medications”; Marcel Dekker, Inc.; 1987. Lipp et al. WO94/04157 3 Mar. 1994). For example, a solution or suspension of a compound of Formula I in a suitable volatile solvent optionally containing penetration enhancing agents can be combined with additional additives known to those skilled in the art, such as matrix materials and bacteriocides. After sterilization, the resulting mixture can be formulated following known procedures into dosage forms. In addition, on treatment with emulsifying agents and water, a solution or suspension of a compound of Formula I may be formulated into a lotion or salve.
  • [0120]
    Suitable solvents for processing transdermal delivery systems are known to those skilled in the art, and include lower alcohols such as ethanol or isopropyl alcohol, lower ketones such as acetone, lower carboxylic acid esters such as ethyl acetate, polar ethers such as tetrahydrofuran, lower hydrocarbons such as hexane, cyclohexane or benzene, or halogenated hydrocarbons such as dichloromethane, chloroform, trichlorotrifluoroethane, or trichlorofluoroethane. Suitable solvents may also include mixtures of one or more materials selected from lower alcohols, lower ketones, lower carboxylic acid esters, polar ethers, lower hydrocarbons, halogenated hydrocarbons.
  • [0121]
    Suitable penetration enhancing materials for transdermal delivery system are known to those skilled in the art, and include, for example, monohydroxy or polyhydroxy alcohols such as ethanol, propylene glycol or benzyl alcohol, saturated or unsaturated C8-C18 fatty alcohols such as lauryl alcohol or cetyl alcohol, saturated or unsaturated C8-C18 fatty acids such as stearic acid, saturated or unsaturated fatty esters with up to 24 carbons such as methyl, ethyl, propyl, isopropyl, n-butyl, sec-butyl isobutyl tertbutyl or monoglycerin esters of acetic acid, capronic acid, lauric acid, myristinic acid, stearic acid, or palmitic acid, or diesters of saturated or unsaturated dicarboxylic acids with a total of up to 24 carbons such as diisopropyl adipate, diisobutyl adipate, diisopropyl sebacate, diisopropyl maleate, or diisopropyl fumarate. Additional penetration enhancing materials include phosphatidyl derivatives such as lecithin or cephalin, terpenes, amides, ketones, ureas and their derivatives, and ethers such as dimethyl isosorbid and diethyleneglycol monoethyl ether. Suitable penetration enhancing formulations may also include mixtures of one or more materials selected from monohydroxy or polyhydroxy alcohols, saturated or unsaturated C1-C18 fatty alcohols, saturated or unsaturated C1-C18 fatty acids, saturated or unsaturated fatty esters with up to 24 carbons, diesters of saturated or unsaturated discarboxylic acids with a total of up to 24 carbons, phosphatidyl derivatives, terpenes, amides, ketones, ureas and their derivatives, and ethers.
  • [0122]
    Suitable binding materials for transdermal delivery systems are known to those skilled in the art and include polyacrylates, silicones, polyurethanes, block polymers, styrenebutadiene coploymers, and natural and synthetic rubbers. Cellulose ethers, derivatized polyethylenes, and silicates may also be used as matrix components. Additional additives, such as viscous resins or oils may be added to increase the viscosity of the matrix.
  • [0123]
    Phamaceutical compositions of the invention may also be in the form of oil-in-water emulsions. The oil phase may be a vegetable oil, for example olive oil or arachis oil, or a mineral oil, for example liquid paraffin or mixtures of these. Suitable emulsifying agents may be naturally-occurring gums, for example gum acacia or gum tragacanth, naturally-occurring phosphatides, for example soy bean, lecithin, and esters or partial esters derived from fatty acids and hexitol anhydrides, for example sorbitan monooleate, and condensation products of the said partial esters with ethylene oxide, for example polyoxyethylene sorbitan monooleate. The emulsions may also contain sweetening and flavoring agents.
  • [0124]
    Syrups and elixirs may be formulated with sweetening agents, for example glycerol, propylene glycol, sorbitol or sucrose. Such formulations may also contain a demulcent, a preservative and flavoring and coloring agents.
  • [0125]
    The compounds may also be administered in the form of suppositories for rectal administration of the drug. These compositions can be prepared by mixing the drug with a suitable non-irritating excipient which is solid at ordinary temperatures but liquid at the rectal or vaginal temperature and will therefore melt in the rectum or vagina to release the drug. Such materials include cocoa butter and polyethylene glycols.
  • [0126]
    For all regimens of use disclosed herein for compounds of Formula I, the daily oral dosage regimen will preferably be from 0.01 to 200 mg/Kg of total body weight. The daily dosage for administration by injection, including intravenous, intramuscular, subcutaneous and parenteral injections, and use of infusion techniques will preferably be from 0.01 to 200 mg/Kg of total body weight. The daily vaginal dosage regimen will preferably be from 0.01 to 200 mg/Kg of total body weight. The daily rectal dosage regimen will preferably be from 0.01 to 200 mg/Kg of total body weight. The transdermal concentration will preferably be that required to maintain a daily dose of from 0.01 to 200 mg/Kg. The daily topical dosage regimen will preferably be from 0.1 to 200 mg administered between one to four times daily. The daily inhalation dosage regimen will preferably be from 0.01 to 10 mg/Kg of total body weight.
  • [0127]
    It will be appreciated by those skilled in the art that the particular method of administration will depend on a variety of factors, all of which are considered routinely when administering therapeutics. It will also be understood, however, that the specific dose level for a given patient depends on a variety of factors, including specific activity of the compound administered, the age of the patient, the body weight of the patient, the general health of the patient, the gender of the patient, the diet of the patient, time of administration, route of administration, rate of excretion, drug combination, and the severity of the condition undergoing therapy, etc. It will be further appreciated by one skilled in the art that the optimal course of treatment, i.e., the mode of treatment and the daily number of doses of a compound of Formula I or a pharmaceutically acceptable salt thereof given for a defined number of days, can be ascertained by those skilled in the art using conventional course of treatment tests.
  • [0128]
    The compounds of FIG. I are producible from known compounds (or from starting materials which, in turn, are producible from known compounds), e.g., through the general preparative methods shown above, The activity of a given compound to inhibit raf kinase can be routinely assayed, e.g., according to procedures disclosed below. The following examples are for illustrative purposes only and are not intended, nor should they be construde to limit the invention in any way.
  • [0129]
    The entire disclosure of all applications, patents and publications cited above and below are hereby incorporated by reference, including provisional application serial number attorney docket number Bayer 10-V1, filed on Dec. 22, 1997 as Ser. No. 08/995,749, and converted on Dec. 22, 1998.
  • [0130]
    The following examples are for illustrative purposes only and are not intended, nor should they be construed to limit the invention in any way.
  • EXAMPLES
  • [0131]
    All reactions were performed in flame-dried or oven-dried glassware under a positive pressure of dry argon or dry nitrogen, and were stirred magnetically unless otherwise indicated. Sensitive liquids and solutions were transferred via syringe or cannula, and introduced into reaction vessels through rubber septa. Unless otherwise stated, the term ‘concentration under reduced pressure’ refers to use of a Buchi rotary evaporator at approximately 15 mmHg.
  • [0132]
    All temperatures are reported uncorrected in degrees Celsius (° C.). Unless otherwise indicated, all parts and percentages are by weight.
  • [0133]
    Commercial grade reagents and solvents were used without further purification. Thin-layer chromatography (TLC) was performed using WhatmanŽ pre-coated glass-backed silica gel 60A F-254 250 μm plates. Visualization of plates was effected by one or more of the following techniques: (a) ultraviolet illumination, (b) exposure to iodine vapor, (c) immersion of the plate in a 10% solution of phosphomolybdic acid in ethanol followed by heating, (d) immersion of the plate in a cerium sulfate solution followed by heating, and/or (e) immersion of the plate in an acidic ethanol solution of 2,4-dinitrophenylhydrazine followed by heating. Column chromatography (flash chromatography) was performed using 230-400 mesh EM ScienceŽ silica gel.
  • [0134]
    Melting points (mp) were determined using a Thomas-Hoover melting point apparatus or a Mettler FP66 automated melting point apparatus and are uncorrected. Fourier transform infrared sprectra were obtained using a Mattson 4020 Galaxy Series spectrophotometer. Proton (1H) nuclear magnetic resonance (NMR) spectra were measured with a General Electric GN-Omega 300 (300 MHz) spectrometer with either Me4Si (d 0.00) or residual protonated solvent (CHCl3 δ 7.26; MeOH δ 3.30; DMSO δ 2.49) as standard. Carbon (13C) NMR spectra were measured with a General Electric ON-Omega 300 (75 MHz) spectrometer with solvent (CDCl3 δ 77.0; MeOD-d3δ 49.0; DMSO-d6 δ 39.5) as standard. Low resolution mass spectra (MS) and high resolution mass spectra (HRMS) were either obtained as electron impact (EI) mass spectra or as fast atom bombardment (FAB) mass spectra. Electron impact mass spectra (EI-MS) were obtained with a Hewlett Packard 5989A mass spectrometer equipped with a Vacumetrics Desorption Chemical Ionization Probe for sample introduction. The ion source was maintained at 250° C. Electron impact ionization was performed with electron energy of 70 eV and a trap current of 300 μA. Liquid-cesium secondary ion mass spectra (FAB-MS), an updated version of fast atom bombardment were obtained using a Kratos Concept 1-H spectrometer. Chemical ionization mass spectra (CI-MS) were obtained using a Hewlett Packard MS-Engine (5989A) with methane or ammonia as the reagent gas (1×10−4 torr to 2.5×10−4 torr). The direct insertion desorption chemical ionization (DCI) probe (Vacuumetrics, Inc.) was ramped from 0-1.5 amps in 10 sec and held at 10 amps until all traces of the sample disappeared (˜1-2 min). Spectra were scanned from 50-800 amu at 2 sec per scan. HPLC-electrospray mass spectra (HPLC ES-MS) were obtained using a Hewlett-Packard 1100 HPLC equipped with a quaternary pump, a variable wavelength detector, a C-18 column, and a Finnigan LCQ ion trap mass spectrometer with electrospray ionization. Spectra were scanned from 120-800 amu using a variable ion time according to the number of ions in the source. Gas chromatography-ion selective mass spectra (GC-MS) were obtained with a Hewlett Packard 5890 gas chromatograph equipped with an HP-1 methyl silicone column (0.33 mM coating; 25 m×0.2 mm) and a Hewlett Packard 5971 Mass Selective Detector (ionization energy 70 eV). Elemental analyses are conducted by Robertson Microlit Labs, Madison N.J.
  • [0135]
    All compounds displayed NMR spectra, LRMS and either elemental analysis or HRMS consistant with assigned structures.
  • LIST OF ABBREVIATIONS AND ACRONYMS
  • [0136]
    AcOH acetic acid
    anh anhydrous
    BOC tert-butoxycarbonyl
    conc concentrated
    dec decomposition
    DMPU 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone
  • DMF N,N-dimethylformamide
  • [0137]
    DMSO dimethylsulfoxide
    DPPA diphenylphosphoryl azide
    EtOAc ethyl acetate
    EtOH ethanol (100%)
    Et2O diethyl ether
    Et3N triethylamine
    m-CPBA 3-chloroperoxybenzoic acid
    MeOH methanol
    pet. ether petroleum ether (boiling range 30-60° C.)
    THF tetrahydrofuran
    TFA trifluoroacetic acid
    Tf trifluoromethanesulfonyl
  • A. General Methods for Synthesis of Substituted Anilines A1. Synthesis of 2,5-Dioxopyrrolidinylanilines
  • [0138]
  • [0139]
    Step 1. 4-tert-Butyl-1-(2,5-dioxo-1-pyrrolidinyl)-2-nitrobenzene: To a solution of 4-tert-butyl-2-nitroaniline (1.04 g, 5.35 mmol) in xylene (25 mL) was added succinic anhydride (0.0535 g, 5.35 mmol) and triethylamine (0.75 mL, 5.35 mmol). The reaction mixture was heated at the reflux temp. for 24 h, cooled to room temp. and diluted with Et2O (25 mL). The resulting mixture was sequentially washed with a 10% HCl solution (50 mL), a saturated NH4Cl solution (50 mL) and a saturated NaCl solution (50 mL), dried (MgSO4), and concentrated under reduced pressure. The residue was purified by flash chromatography (60% EtOAc/40% hexane) to yield the succinimide as a yellow solid (1.2 g, 86%): mp 135-138° C.; 1H NMR(CHCl3) δ 1.38 (s, 9H), 2.94-2.96 (m, 4H), 7.29-7.31 (m, 1H), 7.74-7.78 (m, 1H), 8.18-8.19 (m, 1H).
  • [0000]
  • [0140]
    Step 2. 5-tert-Butyl-2-(2,5-dioxo-1-pyrrolidinyl)aniline: To a solution of 4-tert-butyl-1-(2,5-dioxo-1-pyrrolidinyl)-2-nitrobenzene (1.1 g, 4.2 mmol in EtOAc (25 mL) was added a 10% Pd/C (0.1 g). The resulting slurry was placed under a H2 atmosphere using 3 cycles of an evacuate-quench protocol and was allowed to stir under a H2 atmosphere for 8 h. The reaction mixture was filtered through a pad of CeliteŽ and the residue was washed with CHCl3. The combined filtrate was concentrated under reduced pressure to yield the desired aniline as an off-white solid (0.75 g, 78%); mp 208-211° C.; 1H-NMR (DMSO-d6) δ 1.23 (s, 9H), 2.62-2.76 (m, 4H), 5.10 (br s, 2H), 6.52-6.56 (m, 1H), 6.67-6.70 (m, 2H).
  • A2. General Method for the Synthesis of Tetrahydrofuranyloxyanilines
  • [0141]
  • [0142]
    Step 1. 4-tert-Butyl-1-(3-tetrahydrofuranyloxy)-2-nitrobenzene: To a solution of 4-tert-butyl-2-nitrophenol (1.05 g, 5.4 mmol) in anh THF (25 mL) was added 3-hydroxytetrahydrofuran (0.47 g, 5.4 mmol) and triphenylphosphine (1.55 g, 5.9 mmol) followed by diethyl azodicarboxylate (0.93 ml, 5.9 mmol) and the mixture was allowed to stir at room temp. for 4 h. The resulting mixture was diluted with Et2O (50 mL) and washed with a saturated NH4Cl solution (50 mL) and a saturated NaCl solution (50 mL), dried (MgSO4), and concentrated under reduced pressure. The residue was purified by flash chromatography (30% EtOAc/70% hexane) to yield the desired ether as a yellow solid (1.3 g, 91%): 1H-NMR (CHCl3) δ 1.30 (s, 9H), 2.18-2.24 (m, 2H), 3.91-4.09 (m, 4H), 5.00-5.02 (m, 1H), 6.93 (d, J=8.8 Hz, 1H), 7.52 (dd, J=2.6, 8.8 Hz, 1H), 7.81 (d, J=2.6 Hz, 1H).
  • [0000]
  • [0143]
    Step 2. 5-tert-Butyl-2-(3-tetrahydrofuranyloxy) aniline: To a solution of 4-tert-butyl-1-(3-tetrahydrofuranyloxy)-2-nitrobenzene (1.17 g, 4.4 mmol) in EtOAc (25 mL) was added 10% Pd/C (0.1). The resulting slurry was placed under a H2 atmosphere using 3 cycles of an evacuate-quench protocol and was allowed to stir under a H2 atmosphere for 8 h. The reaction mixture was filtered through a pad of CeliteŽ and washed with CHCl3. The combined filtrate was concentrated under reduced pressure to yield of the desired aniline as a yellow solid (0.89 g, 86%): mp 79-82° C.; 1H-NMR (CHCl3) δ 1.30 (s, 9H), 2.16-2.20 (m, 2H), 3.78 (br s, 2H), 3.85-4.10 (m, 4H), 4.90 (m, 1H), 6.65-6.82 (m, 3H).
  • A3. General Method for the Synthesis of Trifluoromethanesulfonylanilines
  • [0144]
  • [0145]
    Step 1. 2-Methoxy-5-(fluorosulfonyl)acetanilide: Acetic anhydride (0.90 mL, 9.6 mmol) was added to a solution of 4-methoxymetanilyl fluoride (1.0 g, 4.8 mmol) in pyridine (15 mL). After being stirred at room temp. for 4 h, the reaction mixture was concentrated under reduced pressure. The resulting residue was dissolved in CH2Cl2 (25 mL), washed with a saturated NaHCO3 solution (25 ml), dried (Na2SO4), and concentrated under reduced pressure to give a foam which was triturated with a Et2O/hexane solution to provide the title compound (0.85 g); 1H-NMR (CDCl3) δ 2.13 (s, 3H), 3.98 (s, 3H), 7.36 (d, J=8.5 Hz, 1H), 7.82 (dd, J=2.6, 8.8 Hz, 1H), 8.79 (d, J=2.2 Hz, 1H), 9.62 (br s, 1H).
  • [0000]
  • [0146]
    Step 2. 2-Methoxy-5-(trifluoromethanesulfonyl)acetanilide: To an ice-cooled suspension of tris(dimethylamino)sulfonium difluorotrimethylsiliconate (0.094 g, 0.34 mmol) in THF (4 mL) was added a solution of (trifluoromethyl)trimethylsilane (1.0 mL, 6.88 mmol) in THF (3 mL) followed by a solution of 2-methoxy-5-(fluorosulfonyl)acetanilide (0.85 g, 3.44 mmol) in THF (3 mL). The reaction mixture was stirred for 2 h on an ice bath, then was allowed to warm to room temp. and was then concentrated under reduced pressure. The resulting residue was dissolved in CH2Cl2 (25 mL), washed with water (25 mL), dried (Na2SO4), and concentrated under reduced pressure. The resulting material was purified by flash chromatography (3% MeOH/97% CH2Cl2) to provide the title compound as a white solid (0.62 g): 1H-NMR (CDCl3) δ 2.13 (s, 3H) 4.00 (s, 3H), 7.42 (d, J=8.8 Hz, 1H), 7.81 (dd, J=2.6, 8.8 Hz, 1H), 8.80 (d, J=2.2 Hz, 1H), 9.64 (br s, 1H); FAB-MS m/z 298 ((M+1)+).
  • [0000]
  • [0147]
    Step 3. 2-Methoxy-5-(trifluoromethanesulfonyl)aniline: A solution of 2-methoxy-5-(trifluoromethanesulfonyl)acetanilide (0.517 g, 1.74 mmol) in EtOH (5 mL) and a 1 N HCl solution (5 mL) was heated at the reflux temp. for 4 h and the resulting mixture was concentrated under reduced pressure. The residue was dissolved in CH2Cl2 (30 mL), washed with water (30 mL), dried (Na2SO4), and concentrated under reduced pressure to afford the title compound as a gum (0.33 g): 1H-NMR (CDCl3) δ 3.90 (s, 3H) 5.57 (br s, 2H), 7.11-7.27 (m, 3H); FAB-MS m/z 256 ((M+1)+). This material was used in urea formation without further purification.
  • A4. General Method for Aryl Amine Formation via Phenol Nitration Followed by Ether Formation and Reduction
  • [0148]
  • [0149]
    Step 1. 2-Nitro-5-tert-butylphenol; A mixture of timing nitric acid (3.24 g, 77.1 mmol) in glacial HOAc (10 mL) was added dropwise to a solution of m-tert-butylphenol (11.58 g, 77.1 mmol) in glacial HOAc (15 mL) at 0° C. The mixture was allowed to stir at 0° C. for 15 min then warmed to room temp. After 1 h the mixture was poured into ice water (100 mL) and extracted with Et2O (2×50 mL). The organic layer was washed with a saturated NaCl solution (100 mL), dried (MgSO4) and concentrated in vacuo. The residue was purified by flash chromatography (30% EtOAc/70% hexane) to give the desired phenol (4.60 g, 31%): 1H-NMR (DMSO-d6) δ 1.23 (s, 9H), 7.00 (dd, J=1.84, 8.83 Hz, 1H), 7.07 (d, J=1.84 Hz, 1H), 7.82 (d, J=8.83 Hz, 1H), 10.74 (s, 1H).
  • [0000]
  • [0150]
    Step 2. 2-Nitro-5-tert-butylanisole: A slurry of 2-nitro-5-tert-butylphenol (3.68 g, 18.9 mmol) and K2CO3 (3.26 g, 23.6 mmol) in anh DMF (100 mL) was stirred at room temp with stirring for 15 min then treated with iodomethane (2.80 g, 19.8 mmol) via syringe. The reaction was allowed to stir at room temp for 18 h., then was treated with water (100 mL) and extracted with EtOAc (2×100 mL). The combined organic layers were washed with a saturated NaCl solution (50 mL), dried (MgSO4) and concentrated in vacuo to give the desired ether (3.95 g, 100%): 1H-NMR (DMSO-d6) δ 1.29 (s, 9H), 3.92 (s, 3H), 7.10 (dd, J=1.84, 8.46 Hz, 1H), 7.22 (d, J=1.84 Hz, 1H), 7.79 (d, J=8.46 Hz, 1H). This material was used in the next step without further purification.
  • [0000]
  • [0151]
    Step 3. 4-tert-Butyl-2-methoxyaniline: A solution of 2-nitro-5-tert-butylanisole (3.95 g, 18.9 mmol) in MeOH (65 mL) and added to a flask containing 10% Pd/C in MeOH (0.400 g), then placed under a H2 atmosphere (balloon). The reaction was allowed to stir for 18 h at room temp, then filtered through a pad of CeliteŽ and concentrated in vacuo to afford the desired product as a dark sticky solid (3.40 g, 99%): 1H-NMR (DMSO-d6) δ 1.20 (s, 9H), 3.72 (s, 3H), 4.43 (br s, 2H), 6.51 (d, J=8.09 Hz, 1H), 6.64 (dd, J=2.21, 8.09 Hz, 1H), 6.76 (d, J=2.21 Hz, 1H).
  • A5. General Method for Aryl Amine Formation via Carboxylic Acid Esterification Followed by Reduction
  • [0152]
  • [0153]
    Step 1. Methyl 2-Nitro-4-(trifluoromethyl)benzoate: To a solution of 2-nitro-4-(trifluoromethyl)benzoic acid (4.0 g, 17.0 mmol) in MeOH (150 mL) at room temp was added conc H2SO4 (2.5 mL). The mixture was heated at the reflux temp for 24 h., cooled to room temp and concentrated in vacuo. The residue was diluted with water (100 mL) and extracted with EtOAc (2×100 mL). The combined organic layers were washed with a saturated NaCl solution, dried (MgSO4), concentrated in vacuo. The residue was purified by flash chromatography (14% EtOAc/86% hexane) to give the desired ester as a pale yellow oil (4.17 g, 98%): 1H-NMR (DMSO-d6) δ 3.87 (s, 3H), 8.09 (d, J=7.72 Hz, 1H), 8.25 (dd, J=1.11, 8.09 Hz, 1H), 8.48 (d, J=1.11 Hz, 1H).
  • [0000]
  • [0154]
    Step 2. Methyl 2-Amino-4-(trifluoromethyl)benzoate; A solution of methyl 2-nitro-4-(trifluoromethyl)benzoate (3.90 g, 15.7 mmol) in EtOAc (100 mL) and added to a flask containing 10% Pd/C (0.400 mg) in EtOAc (10 mL), then placed under a H2 atmosphere (balloon). The reaction was allowed to stir for 18 h at room temp, then was filtered through CeliteŽ and concentrated in vacuo to afford the desired product as a white crystalline solid (3.20 g, 93%): 1H-NMR (DMSO-d6) δ 3.79 (s, 3H), 6.75 (dd, J=1.84, 8.46 Hz, 1H), 6.96 (br s, 2H), 7.11 (d, J=0.73 Hz, 1H), 7.83 (d, J=8.09 Hz, 1H).
  • A6. General Method for Aryl Amine Formation via Ether Formation Followed Ester Saponification, Curtius Rearrangement, and Carbamate Deprotection
  • [0155]
  • [0156]
    Step 1. Methyl 3-Methoxy-2-naphthoate, A slurry of methyl 3-hydroxy-2-naphthoate (10.1 g, 50.1 mmol) and K2CO3 (7.96 g, 57.6 mmol) in DMF (200 mL) was stirred at room temp for 15 min, then treated with iodomethane (3.43 mL, 55.1 mmol). The mixture was allowed to stir at room temp overnight, then was treated with water (200 ml). The resulting mixture was extracted with EtOAc (2×200 mL). The combined organic layers were washed with a saturated NaCl solution (100 mL), dried (MgSO4), concentrated in vacuo (approximately 0.4 mmHg overnight) to give the desired ether as an amber oil (10.30 g): 1H-NMR (DMSO-d6) δ 2.70 (s, 3H), 2.85 (s, 3H), 7.38 (app t, J=8.09 Hz, 1H), 7.44 (s, 1H), 7.53 (app t, J=8.09 Hz, 1H), 7.84 (d, J=8.09 Hz, 1H), 7.90 (s, 1H), 8.21 (s, 1H).
  • [0000]
  • [0157]
    Step 2. 3-Methoxy-2-naphthoic Acid: A solution of methyl 3-methoxy-2-naphthoate (6.28 g, 29.10 mmol) and water (10 mL) in MeOH (100 mL) at room temp was treated with a 1 N NaOH solution (33.4 mL, 33.4 mmol). The mixture was heated at the reflux temp for 3 h, cooling to room temp, and made acidic with a 10% citric acid solution. The resulting solution was extracted with EtOAc (2×100 mL). The combined organic layers were washed with a saturated NaCl solution, dried (MgSO4) and concentrated in vacuo. The residue was triturated with hexanes and washed several times with hexanes to give the desired carboxylic acid as a white crystalline solid (5.40 g, 92%): 1H-NMR (DMSO-d6) δ 3.88 (s, 3H), 7.34-7.41 (m, 2H), 7.49-7.54 (m, 1H), 7.83 (d, J=8.09 Hz, 1H), 7.91 (d, J=8.09 Hz, 1H), 8.19 (s, 1H), 12.83 (br s, 1H).
  • [0000]
  • [0158]
    Step 3. 2-(N—(Carbobenzyloxy)amino-3-methoxynaphthalene: A solution of 3-methoxy-2-naphthoic acid (3.36 g, 16.6 mmol) and Et3N (2.59 mL, 18.6 mmol) in anh toluene (70 mL) was stirred at room temp. for 15 min., then treated with a solution of diphenylphosphoryl azide (5.12 g, 18.6 mmol) in toluene (10 mL) via pipette. The resulting mixture was heated at 80° C. for 2 h. After cooling the mixture to room temp. benzyl alcohol (2.06 mL, 20 mmol) was added via syringe. The mixture was then warmed to 80° C. overnight. The resulting mixture was cooled to room temp., quenched with a 10% citric acid solution, and extracted with EtOAc (2×100 mL). The combined organic layers were washed with a saturated NaCl solution, dried (MgSO4), and concentrated in vacuo. The residue was purified by flash chromatography (14% EtOAc/86% hexane) to give the benzyl carbamate as a pale yellow oil (5.1 g, 100%): 1H-NMR (DMSO-d6) δ 3.89 (s, 3H), 5.17 (s, 2H), 7.27-7.44 (m, 8H), 7.72-7.75 (m, 2H), 8.20 (s, 1H), 8.76 (s, 1H).
  • [0000]
  • [0159]
    Step 4. 2-Amino-3-methoxynaphthalene: A slurry of 2-(N-(carbobenzyloxy)amino-3-methoxynaphthalene (5.0 g, 16.3 mmol) and 10% Pd/C (0.5 g) in EtOAc (70 mL) was maintained under a H2 atmospheric (balloon) at room temp. overnight. The resulting mixture was filtered through CeliteŽ and concentrated in vacuo to give the desired amine as a pale pink powder (2.40 g, 85%): 1H-NMR (DMSO-d6) δ 3.86 (s, 3H), 6.86 (s, 2H), 7.04-7.16 (m, 2H), 7.43 (d, J=8.0 Hz, 1H), 7.56 (d, J=8.0 Hz, 1H); EI-MS m/z 173 (M+).
  • A7. General Method for the Synthesis of Aryl Amines via Metal-Mediated Cross Coupling Followed by Reduction
  • [0160]
  • [0161]
    Step 1. 5-tert-Butyl-2-(trifluoromethanesulfonyl)oxy-1-nitrobenzene: To an ice cold solution of 4-tert-butyl-2-nitrophenol (6.14 g, 31.5 mmol) and pyridine (10 mL, 125 mmol) in CH2Cl2 (50 mL) was slowly added trifluoromethanesulfonic anhydride (10 g, 35.5 mmol) via syringe. The reaction mixture was stirred for 15 min, then allowed to warm up to room temp. and diluted with CH2Cl2 (100 mL). The resulting mixture was sequentially washed with a 1M NaOH solution (3×100 mL), and a 1M HCl solution (3×100 mL), dried (MgSO4), and concentrated under reduced pressure to afford the title compound (8.68 g, 84%): 1H-NMR (CDCl3) δ 1.39 (s, 9H), 7.30-8.20 (m, 3H).
  • [0000]
  • [0162]
    Step 2. 5-tert-Butyl-2-(3-fluorophenyl)-1-nitrobenzene: A mixture of 3-fluorobenzeneboronic acid (3.80 g, 27.5 mmol), KBr (2.43 g, 20.4 mmol), K3PO4 (6.1 g, 28.8 mmol), and Pd(PPh3)4 (1.0 g, 0.9 mmol) was added to a solution of 5-tert-butyl-2-(trifluoromethanesulfonyl)oxy-1-nitrobenzene (6.0 g, 18.4 mmol) in dioxane (100 mL). The reaction mixture was heated at 80° C. for 24 h, at which time TLC indicated complete reaction. The reaction mixture was treated with a saturated NH4Cl solution (50 mL) and extracted EtOAc (3×100 mL). The combined organic layers were dried (MgSO4) and concentrated under reduced pressure. The residue was purified by flash chromatography (3% EtOAc/97% hexane) to give the title compound (4.07 g, 81%): 1H-NMR (CDCl3) δ 1.40 (s, 9H), 6.90-7.90 (m, 7H).
  • [0000]
  • [0163]
    Step 3. 5-tert-Butyl-2-(3-fluorophenyl)aniline: To a solution of 5-tert-butyl-2-(3-fluorophenyl)-1-nitrobenzene (3.5 g, 12.8 mmol) and EtOH (24 mL) in EtOAc (96 mL) was added 5% Pd/C (0.350 g) and the resulting slurry was stirred under a H2 atmosphere for 24 h, at which time TLC indicated complete consumption of starting material. The reaction mixture was filtered through a pad of CeliteŽ to give the desired product (2.2 g, 72%): 1H-NMR (CDCl3) δ 1.35 (s, 9H), 3.80 (br s, 2H), 6.90-7.50 (m, 7H).
  • A8. General Method for the Synthesis of Nitroanilines
  • [0164]
  • [0165]
    Step 1. 4-(4-(2-Propoxycarbonylamino)phenyl)methylaniline: A solution of di-tert-butyl dicarbonate (2.0 g, 9.2 mmol) and 4,4′-methylenedianiline (1.8 g, 9.2 mmol) in DMF (100 mL) was heated at the reflux temp. for 2 h, then cooled to room temp. This mixture was diluted with EtOAc (200 mL) sequentially washed with a saturated NH4Cl (200 mL) and a saturated NaCl solution (100 mL), and dried (MgSO4). The residue was purified by flash chromatography (30% EtOAc/70% hexane) to give the desired carbamate (1.3 g, 48%): 1H-NMR (CDCl3) δ 1.51 (s, 9H), 3.82 (s, 2H), 6.60-7.20 (m, 8H).
  • [0000]
  • [0166]
    Step 2. 4-(4-(2-Propoxycarbonylamino)phenyl)methyl-1-nitrobenzene: To an ice cold solution of 4-(4-(2-propoxycarbonylamino)phenyl)methylaniline (1.05 g, 3.5 mmol) in CH2Cl2 (15 mL) was added m-CPBA (1.2 g, 7.0 mmol). The reaction mixture was slowly allowed to warm to room temp. and was stirred for 45 min, at which time TLC indicated disappearance of starting material. The resulting mixture was diluted with EtOAc (50 mL), sequentially washed with a 1M NaOH solution (50 mL) and a saturated NaCl solution (50 mL), and dried (MgSO4). The residue was purified by flash chromatography (20% EtOAc/80% hexane) to give the desired nitrobenzene (0.920 g): FAB-MS m/z 328 (M+).
  • [0000]
  • [0167]
    Step 3. 4-(4-Nitrophenyl)methylaniline: To a solution of 4-(4-(2-propoxycarbonylamino)phenyl)methyl-1-nitrobenzene (0.920 g, 2.8 mmol) in dioxane (10 mL) was added a conc. HCl solution (4.0 mL) and the resulting mixture was heated at 80° C. for 1 h at which time TLC indicated disappearance of starting material. The reaction mixture was cooled to room temp. The resulting mixture was diluted with EtOAc (50 mL), then washed with a 1M NaOH solution (3×50 mL), and dried (MgSO4) to give the desired aniline (0.570 mg, 89%): 1H-NMR (CDCl3) δ 3.70 (br s, 2H), 3.97 (s, 2H), 6.65 (d, J=8.5 Hz, 2H), 6.95 (d, J=8.5 Hz, 2H), 7.32 (d, J=8.8 Hz, 2H), 8.10 (d, J=8.8 Hz, 2H).
  • A9. General Method for Synthesis of Aryl Anilines via Alkylation of a Nitrophenol Followed by Reduction
  • [0168]
  • [0169]
    Step 1. 4-(α-Bromoacetyl)morpholine: To an ice cold solution of morpholine (2.17 g, 24.9 mmol) and diisopropylethylamine (3.21 g, 24.9 mmol) in CH2Cl2 (70 mL) was added a solution of bromoacetyl bromide (5.05 g, 25 mmole) in CH2Cl2 (8 mL) via syringe. The resulting solution was kept at 0° C. for 45 min, then was allowed to warm to room temp. The reaction mixture was diluted with EtOAc (500 mL), sequentially washed with a 1M HCl solution (250 mL) and a saturated NaCl solution (250 mL), and dried (MgSO4) to give the desired product (3.2 g, 62%): 1H-NMR (DMSO-d6) δ 3.40-3.50 (m, 4H), 3.50-3.60 (m, 4H), 4.11 (s, 2H)
  • [0000]
  • [0170]
    Step 2. 2-(N-Morpholinylcarbonyl)methoxy-5-tert-butyl-1-nitrobenzene: A slurry of 4-tert-butyl-2-nitrophenol (3.9 g, 20 mmol) and K2CO3 (3.31 g, 24 mmol) in DMF (75 mL) was stirred at room temp. for 15 minutes, then a solution of 4-(α-bromoacetyl)morpholine (4.16 g, 20 mmol) in DMF (10 mL) was added. The reaction was allowed to stir at room temp. overnight, then was diluted with EtOAc (500 mL) and sequentially washed with a saturated NaCl solution (4×200 mL) and a 1M NaOH solution (400 mL). The residue was purified by flash chromatography (75% EtOAc/25% hexane) to give the nitrobenzene (2.13 g, 33%): 1H-NMR (DMSO-d6) δ 1.25 (s, 9H), 3.35-3.45 (m, 4H), 3.50-3.58 (m, 4H), 5.00 (s, 2H), 7.12 (d, J=8.8 Hz, 1H), 7.50-7.80 (m, 2H).
  • [0000]
  • [0171]
    Step 3. 2-(N-Morpholinylcarbonyl)methoxy-5-tert-butylanline: To a solution of 2-(N-morpholinaylcarbonyl)methoxy-5-tert-butyl-1-nitrobenzene (2.13 g, 6.6 mmol) and EtOH (10 mL) in EtOAc (40 mL) was added 5% Pd/C (0.215 g), The resulting slurry was stirred under a H2 atmosphere for 6 h, at which time TLC indicated complete consumption of starting material. The reaction mixture was filtered through a pad of CeliteŽ to give the desired product (1.9 g, 98%): 1H-NMR (DMSO-d6) δ 1.18 (s, 9H), 3.40-3.50 (m, 4H), 3.50-3.60 (m, 4H), 4.67 (br s, 2H), 4.69 (s, 2H), 6.40-6.70 (m, 3H).
  • A10. General Method for Aryl Amine Formation via Nitrophenol Alkylation Followed by Reduction
  • [0172]
  • [0173]
    Step 1. 5-tert-Butyl-2-(2-hydroxyethoxy)-1-nitrobenzene: A solution of 4-tert-butyl-2-nitrophenol (30 g, 0.15 mol) and tetra-n-butylammonium fluoride (0.771 g, 3.0 mmol) in ethylene carbonate (10.24 mL. 0.15 mol) was heated at 150° C. for 18 hi, then cooled to room temp. and separated between water (50 mL) and CH2Cl2 (50 mL). The organic layer was dried (MgSO4) and concentrated under reduced pressure. The residue was purified by column chromatography (20% EtOAc/80% hexane) to afford the desired product as a brown oil (35.1 g, 90%): 1H-NMR (DMSO-d6) δ 1.25 (s, 9H), 3.66-3.69 (m, 2H), 4.10-4.14 (t, J=5.0 Hz, 2H), 4.85 (t, J=5.0 Hz, 1H), 7.27 (d, J=8.8 Hz, 1H), 7.60-7.64 (m, 1H), 7.75 (d, J=2.6 Hz, 1H).
  • [0000]
  • [0174]
    Step 2. 5-tert-Butyl-2-(2-tert-butoxycarbonyloxy)ethoxy)-1-nitrobenzene: A solution of 5-tert-butyl-2-(2-hydroxyethoxy)-1-nitrobenzene (0.401 g, 1.68 mmol), di-tert-butyl dicarbonate (0.46 mL, 2.0 mmol) and dimethylaminopyridine (0.006 g, 0.05 mmol) in CH2Cl2 (15 mL) was stirred at room temp. for 30 min, at which time TLC indicated consumption of starting material. The resulting mixture was washed with water (20 mL), dried (MgSO4) and concentrated under reduced pressure. The residue was purified by column chromatography (3% MeOH/97% CH2Cl2) to give the desired product as a yellow oil (0.291 g, 51%): 1H-NMR (DMSO-d6) δ 1.25 (s, 9H), 1.38 (s, 9H), 4.31 (br s, 4H), 7.27 (d, J=9.2 Hz, 1H) 7.64 (dd, J=2.6, 8.8 Hz, 1H) 7.77 (d, J=2.6 Hz, 1H).
  • [0000]
  • [0175]
    Step 3. 5-tert-Butyl-2-(2-tert-butoxycarbonyloxy)ethoxy)aniline: To a mixture of 5-tert-butyl-2-(2-tert-butoxycarbonyloxy)ethoxy)-1-nitrobenzene (0.290 g, 0.86 mmol) and 5% Pd/C (0.058 g) in MeOH (2 mL) was ammonium formate (0.216 g, 3.42 mmol), and the resulting mixture was stirred at room temp. for 12 h, then was filtered through a pad of CeliteŽ with the aid of EtOH. The filtrate was concentrated under reduced pressure and the residue was purified by column chromatography (2% MeOH/98% CH2Cl2) to give the desired product as a pale yellow oil (0.232 g, 87%); TLC (20% EtOAc/80% hexane) R0.63; 1H-NMR (DMSO-d6) δ 1.17 (s, 9H), 1.39 (s, 9H), 4.03-4.06 (m, 2H), 4.30-4.31 (m, 2H), 4.54 (br s, 2H), 6.47 (dd, J=2.2, 8.1 Hz, 1H) 6.64-6.67 (m, 2H).
  • A11. General Method for Substituted Aniline Formation via Hydrogenation of a Nitroarene
  • [0176]
  • [0177]
    4-(4-Pyridinylmethyl)aniline: To a solution of 4-(4-nitrobenzyl)pyridine (7.0 g, 32.68 mmol) in EtOH (200 mL) was added 10% Pd/C (0.7 g) and the resulting slurry was shaken under a H2 atmosphere (50 psi) using a Parr shaker. After 1 h, TLC and 1H-NMR of an aliquot indicated complete reaction. The mixture was filtered through a short pad of CeliteŽ. The filtrate was concentrated in vacuo to afford a white solid (5.4 g, 90%): 1H-NMR (DMSO-d6) δ 3.74 (s, 2H), 4.91 (br s, 2H), 6.48 (d, J=8.46 Hz, 2H), 6.86 (d, J=8.09 Hz, 2H), 7.16 (d, J=5.88 Hz, 2H), 8.40 (d, J=5.88 Hz, 2H); EI-MS m/z 184 (M+) This material was used in urea formation reactions without further purification.
  • A12. General Method for Substituted Aniline Formation via Dissolving Metal Reduction of a Nitroarene
  • [0178]
  • [0179]
    4-(2-Pyridinylthio)aniline. To a solution of 4-(2-pyridinylthio)-1-nitrobenzene (Menai ST 3355A; 0.220 g, 0.95 mmol) and H2O (0.5 mL) in AcOH (5 mL) was added iron powder (0.317 g, 5.68 mmol) and the resulting slurry stirred for 16 h at room temp. The reaction mixture was diluted with EtOAc (75 ml) and H2O (50 mL), basified to pH 10 by adding solid K2CO3 in portions (Caution: foaming). The organic layer was washed with a saturated NaCl solution, dried (MgSO4), concentrated in vacuo. The residual solid was purified by MPLC (30% EtOAc/70% hexane) to give the desired product as a thick oil (0.135 g, 70%): TLC (30% EtOAc/70% hexanes) R20.
  • A13a. General Method for Substituted Aniline Formation via Nitroarene Formation Through Nucleophilic Aromatic Substitution, Followed by Reduction
  • [0180]
  • [0181]
    Step 1. 1-Methoxy-4-(4-nitrophenoxy)benzene: To a suspension of NaH (95%, 1.50 g, 59 mmol) in DMF (100 mL) at room temp. was added dropwise a solution of 4-methoxyphenol (7.39 g, 59 mmol) in DMF (50 mL). The reaction was stirred 1 h, then a solution of 1-fluoro-4-nitrobenzene (7.0 g, 49 mmol) in DMF (50 mL) was added dropwise to form a dark green solution. The reaction was heated at 95° C. overnight, then cooled to room temp., quenched with H2O, and concentrated in vacuo. The residue was partitioned between EtOAc (200 mL) and H2O (200 mL). The organic layer was sequentially washed with H2O (2×200 mL), a saturated NaHCO3 solution (200 mL), and a saturated NaCl solution (200 mL), dried (Na2SO4), and concentrated in vacuo. The residue was triturated (Et2O/hexane) to afford 1-methoxy-4-(4-nitrophenoxy)benzene (12.2 g, 100%): 1H-NMR (CDCl3) δ 3.83 (s, 3H), 6.93-7.04 (m, 6H), 8.18 (d, J=9.2 Hz, 2H); EI-MS m/z 245 (M+).
  • [0000]
  • [0182]
    Step 2. 4-(4-Methoxyphenoxy)aniline: To a solution of 1-methoxy-4-(4-nitrophenoxy)benzene (12.0 g, 49 mmol) in EtOAc (250 mL) was added 5% Pt/C (1.5 g) and the resulting slurry was shaken under a H2 atmosphere (50 psi) for 18 h. The reaction mixture was filtered through a pad of CeliteŽ with the aid of EtOAc and concentrated in vacuo to give an oil which slowly solidified (10.6 g, 100%): 1H-NMR (CDCl3) δ 3.54 (br s, 2H), 3.78 (s, 3H), 6.65 (d, J=8.8 Hz, 2H), 6.79-6.92 (m, 6H); EI-MS m/z 215 (M+).
  • A13b. General Method for Substituted Aniline Formation via Nitroarene Formation Through Nucleophilic Aromatic Substitution, Followed by Reduction
  • [0183]
  • [0184]
    Step 1. 3-(Trifluoromethyl)-4-(4-pyridinylthio)nitrobenzene: A solution of 4-mercaptopyridine (2.8 g, 24 mmoles), 2-fluoro-5-nitrobenzotrifluoride (5 g, 23.5 mmoles), and potassium carbonate (6.1 g, 44.3 mmoles) in anhydrous DMF (80 mL) was stirred at room temperature and under argon overnight. TLC showed complete reaction. The mixture was diluted with Et2O (100 mL) and water (100 mL) and the aqueous layer was back-extracted with Et2O (2×100 mL). The organic layers were washed with a saturated NaCl solution (100 mL), dried (MgSO4), and concentrated under reduced pressure. The solid residue was triturated with Et2O to afford the desired product as a tan solid (3.8 g, 54%): TLC (30% EtOAc/70% hexane) R˜0.06; 1H-NMR (DMSO-d6) δ 7.33 (dd, J=1.2, 4.2 Hz, 2H), 7.78 (d, J==8.7 Hz, 1H), 8.46 (dd, J=2.4, 8.7 Hz, 1H), 8.54-8.56 (m, 3H).
  • [0000]
  • [0185]
    Step 2. 3-(Trifluoromethyl)-4-(4-pyridinylthio)aniline. A slurry of 3-trifluoromethyl-4-(4-pyridinylthio)nitrobenzene (3.8 g, 12.7 mmol), iron powder (4.0 g, 71.6 mmol), acetic acid (100 mL), and water (1 mL) were stirred at room temp. for 4 h. The mixture was diluted with Et2O (100 mL) and water (100 mL). The aqueous phase was adjusted to pH 4 with a 4 N NaOH solution. The combined organic layers were washed with a saturated NaCl solution (100 mL), dried (MgSO4), and concentrated under reduced pressure. The residue was filtered through a pad of silica (gradient from 50% EtOAc/50% hexane to 60% EtOAc/40% hexane) to afford the desired product (3.3 g): TLC (50% EtOAc/50% hexane) R0.10; 1H-NMR (DMSO-d6) δ 6.21 (s, 2H), 6.84-6.87 (m, 3H), 7.10 (d, J=2.4 Hz, 1H), 7.39 (d, J=8.4 Hz, 1H), 8.29 (d, J=6.3 Hz, 2H).
  • A13c. General Method for Substituted Aniline Formation via Nitroarene Formation Through Nucleophilic Aromatic Substitution, Followed by Reduction
  • [0186]
  • [0187]
    Step 1. 4-(2-(4-Phenyl)thiazolyl)thio-1-nitrobenzene: A solution of 2-mercapto-4-phenylthiazole (4.0 g, 20.7 mmoles) in DMF (40 mL) was treated with 1-fluoro-4-nitrobenzene (2.3 ml, 21.7 mmoles) followed by K2CO3 (3.18 g, 23 mmol), and the mixture was heated at approximately 65° C. overnight. The reaction mixture was then diluted with EtOAc (100 mL), sequentially washed with water (100 mL) and a saturated NaCl solution (100 mL), dried (MgSO4) and concentrated under reduced pressure. The solid residue was triturated with a Et2O/hexane solution to afford the desired product (6.1 g): TLC (25% EtOAc/75% hexane) R0.49; 1H-NMR (CDCl3) δ 7.35-7.47 (m, 3H), 7.58-7.63 (m, 3H), 7.90 (d, J=6.9 Hz, 2H), 8.19 (d, J=9.0 Hz, 2H).
  • [0000]
  • [0188]
    Step 2. 4-(2-(4-Phenyl)thiazolyl)thioaniline: 4-(2-(4-Phenyl)thiazolyl)thio-1-nitro-benzene was reduced in a manner analagous to that used in the preparation of 3-(trifluoromethyl)-4-(4-pyridinylthio)aniline: TLC (25% EtOAc/75% hexane) R0.18; 1H-NMR (CDCl3) δ 3.89 (br s, 2H), 6.72-6.77 (m, 2H), 7.26-7.53 (m, 6H), 7.85-7.89 (m, 2H).
  • A13d. General Method for Substituted Aniline Formation via Nitroarene Formation Through Nucleophilic Aromatic Substitution, Followed by Reduction
  • [0189]
  • [0190]
    Step 1. 4-(6-Methyl-3-pyridinyloxy)-1-nitrobenzene: to a solution of 5-hydroxy-2-methylpyridine (5.0 g, 45.8 mmol) and 1-fluoro-4-nitrobenzene (6.5 g, 45.8 mmol) in anh DMF (50 mL) was added K2CO3 (13.0 g, 91.6 mmol) in one portion. The mixture was heated at the reflux temp. with stirring for 18 h and then allowed to cool to room temp. The resulting mixture was poured into water (200 mL) and extracted with EtOAc (3×150 mL). The combined organics were sequentially washed with water (3×100 mL) and a saturated NaCl solution (2×100 mL), dried (Na2SO4), and concentrated in vacuo to afford the desired product (8.7 g, 83%). The this material was carried to the next step without further purification.
  • [0000]
  • [0191]
    Step 2. 4-(6-Methyl-3-pyridinyloxy)aniline: A solution of 4-(6-methyl-3-pyridinyloxy)-1-nitrobenzene (4.0 g, 17.3 mmol) in EtOAc (150 mL) was added to 10% Pd/C (0.500 g, 0.47 mmol) and the resulting mixture was placed under a H2 atmosphere (balloon) and was allowed to stir for 18 h at room temp. The mixture was then filtered through a pad of CeliteŽ and concentrated in vacuo to afford the desired product as a tan solid (3.2 g, 92%): EI-MS m/z 200 (M+).
  • A13e. General Method for Substituted Aniline Formation via Nitroarene Formation Through Nucleophilic Aromatic Substitution, Followed by Reduction
  • [0192]
  • [0193]
    Step 1. 4-(3,4-Dimethoxyphenoxy)-1-nitrobenzene: To a solution of 3,4-dimethoxyphenol (1.0 g, 6.4 mmol) and 1-fluoro-4-nitrobenzene (700 μL, 6.4 mmol) in anh DMF (20 mL) was added K2CO3 (1.8 g, 12.9 mmol) in one portion. The mixture was heated at the reflux temp with stirring for 18 h and then allowed to cool to room temp. The mixture was then poured into water (100 mL) and extracted with EtOAc (3×100 mL). The combined organics were sequentially washed with water (3×50 mL) and a saturated NaCl solution (2×50 mL), dried (Na2SO4), and concentrated in vacuo to afford the desired product (0.8 g, 54%). The crude product was carried to the next step without further purification.
  • [0000]
  • [0194]
    Step 2. 4-(3,4-Dimethoxyphenoxy)aniline: A solution of 4-(3,4-dimethoxy-phenoxy)-1-nitrobenzene (0.8 g, 3.2 mmol) in EtOAc (50 mL) was added to 10% Pd/C (0.100 g) and the resulting mixture was placed under a H2 atmosphere (balloon) and was allowed to stir for 18 h at room temp. The mixture was then filtered through a pad of CeliteŽ and concentrated in vacuo to afford the desired product as a white solid (0.6 g, 75%): EI-MS m/z 245 (M+).
  • A13f. General Method for Substituted Aniline Formation via Nitroarene Formation Through Nucleophilic Aromatic Substitution, Followed by Reduction
  • [0195]
  • [0196]
    Step 1. 3-(3-Pyridinyloxy)-1-nitrobenzene; To a solution of 3-hydroxypyridine (2.8 g, 29.0 mmol), 1-bromo-3-nitrobenzene (5.9 g, 29.0 mmol) and copper(I) bromide (5.0 g, 34.8 mmol) in anh DMF (50 mL) was added K2CO3 (8.0 g, 58.1 mmol) in one portion. The resulting mixture was heated at the reflux temp. with stirring for 18 h and then allowed to cool to room temp. The mixture was then poured into water (200 mL) and extracted with EtOAc (3×150 mL). The combined organics were sequentially washed with water (3×100 mL) and a saturated NaCl solution (2×100 mL), dried Na2SO4), and concentrated in vacuo. The resulting oil was purified by flash chromatography (30% EtOAc/70% hexane) to afford the desired product (2.0 g, 32%). This material was used in the next step without further purification.
  • [0000]
  • [0197]
    Step 2. 3-(3-Pyridinyloxy)aniline: A solution of 3-(3-pyridinyloxy)-1-nitrobenzene (2.0 g, 9.2 mmol) in EtOAc (100 mL) was added to 10% Pd/C (0.200 g) and the resulting mixture was placed under a H2 atmosphere (balloon) and was allowed to stir for 18 h at room temp. The mixture was then filtered through a pad of CeliteŽ and concentrated in vacuo to afford the desired product as a red oil (1.6 g, 94%): EI-MS m/z 186 (M+).
  • A13g. General Method for Substituted Aniline Formation via Nitroarene Formation Through Nucleophilic Aromatic Substitution, Followed by Reduction
  • [0198]
  • [0199]
    Step 1. 3-(5-Methyl-3-pyridinyloxy)-1-nitrobenzene: To a solution of 3-hydroxy-5-methylpyridine (5.0 g, 45.8 mmol), 1-bromo-3-nitrobenzene (12.0 g, 59.6 mmol) and copper(I) iodide (10.0 g, 73.3 mmol) in anh DMF (50 mL) was added K2CO3 (13.0 g, 91.6 mmol) in one portion. The mixture was heated at the reflux temp. with stirring for 18 h and then allowed to cool to room temp. The mixture was then poured into water (200 mL) and extracted with EtOAc (3×150 mL). The combined organics were sequentially washed with water (3×100 mL) and a saturated NaCl solution (2×100 mL), dried (Na2SO4), and concentrated in vacuo. The resulting oil was purified by flash chromatography (30% EtOAc/70% hexane) to afford the desired product (1.2 g, 13%).
  • [0000]
  • [0200]
    Step 2. 3-(5-Methyl-3-pyridinyloxy)-1-nitrobenzene: A solution of 3-(5-methyl-3-pyridinyloxy)-1-nitrobenzene (1.2 g, 5.2 mmol) in EtOAc (50 mL) was added to 10% Pd/C (0.100 g) and the resulting mixture was placed under a H2 atmosphere (balloon) and was allowed to stir for 18 h at room temp. The mixture was then filtered through a pad of CeliteŽ and concentrated in vacuo to afford the desired product as a red oil (0.9 g, 86%): CI-MS m/z 201 ((M+H)+).
  • A13h. General Method for Substituted Aniline Formation via Nitroarene Formation Through Nucleophilic Aromatic Substitution, Followed by Reduction
  • [0201]
  • [0202]
    Step 1. 5-Nitro-2-(4-methylphenoxy)pyridine: To a solution of 2-chloro-5-nitropyridine (6.34 g, 40 mmol) in DMF (200 mL) were added of 4-methylphenol (5.4 g, 50 mmol, 1.25 equiv) and K2CO3 (8.28 g, 60 mmol, 1.5 equiv). The mixture was stirred overnight at room temp. The resulting mixture was treated with water (600 mL) to generate a precipitate. This mixture was stirred for 1 h, and the solids were separated and sequentially washed with a 1 N NaOH solution (25 mL), water (25 mL) and pet ether (25 mL) to give the desired product (7.05 g, 76%): mp 80-82° C.; TLC (30% EtOAc/70% pet ether) R0.79; 1H-NMR (DMSO-d6) δ 2.31 (s, 3H), 7.08 (d, J=8.46 Hz, 2H), 7.19 (d, J=9.20 Hz, 1H), 7.24 (d, J=8.09 Hz, 2H), 8.58 (dd, J=2.94, 8.82 Hz, 1H), 8.99 (d, J=2.95 Hz, 1H); FAB-MS m/z (rel abundance) 231 ((M+H)+), 100%).
  • [0000]
  • [0203]
    Step 2. 5-Amino-2-(4-methylphenoxy)pyridine Dihydrochloride: A solution 5-nitro-2-(4-methylphenoxy)pyridine (6.94 g, 30 mmol, 1 eq) and EtOH (10 mL) in EtOAc (190 mL) was purged with argon then treated with 10% Pd/C (0.60 g). The reaction mixture was then placed under a H2 atmosphere and was vigorously stirred for 2.5 h. The reaction mixture was filtered through a pad of CeliteŽ. A solution of HCl in Et2O was added to the filtrate was added dropwise. The resulting precipitate was separated and washed with EtOAc to give the desired product (7.56 g, 92%): mp 208-210° C. (dec); TLC (50% EtOAc/50% pet ether) R0.42; 1H-NMR (DMSO-d6) δ 2.25 (s, 3H), 6.98 (d, J=8.45 Hz, 2H), 7.04 (d, J=8.82 Hz, 1H), 7.19 (d, J=8.09 Hz, 2H), 8.46 (dd, J=2.57, 8.46 Hz, 1H), 8.63 (d, J=2.57 Hz, 1H); EI-MS m/z (rel abundance) (M+, 100%).
  • A13i. General Method for Substituted Aniline Formation via Nitroarene Formation Through Nucleophilic Aromatic Substitution, Followed by Reduction
  • [0204]
  • [0205]
    Step 1. 4-(3-Thienylthio)-1-nitrobenzene; To a solution of 4-nitrothiophenol (80% pure; 1.2 g, 6.1 mmol), 3-bromothiophene (1.0 g, 6.1 mmol) and copper(II) oxide (0.5 g, 3.7 mmol) in anhydrous DMF (20 mL) was added KOH (0.3 g, 6.1 mmol), and the resulting mixture was heated at 130° C. with stirring for 42 h and then allowed to cool to room temp. The reaction mixture was then poured into a mixture of ice and a 6N HCl solution (200 mL) and the resulting aqueous mixture was extracted with EtOAc (3×100 mL). The combined organic layers were sequentially washed with a 1M NaOH solution (2×100 mL) and a saturated NaCl solution (2×100 mL), dried (MgSO4), and concentrated in vacuo. The residual oil was purified by MPLC (silica gel; gradient from 10% EtOAc/90% hexane to 5% EtOAc/95% hexane) to afford of the desired product (0.5 g, 34%). GC-MS m/z 237 (M+).
  • [0000]
  • [0206]
    Step 2. 4-(3-Thienylthio)aniline: 4-(3-Thienylthio)-1-nitrobenzene was reduced to the aniline in a manner analogous to that described in Method B1.
  • A13j. General Method for Substituted Aniline Formation via Nitroarene Formation Through Nucleophilic Aromatic Substitution, Followed by Reduction
  • [0207]
  • [0208]
    4-(5-Pyrimininyloxy)aniline: 4-Aminophenol (1.0 g, 9.2 mmol) was dissolved in DMF (20 mL) then 5-bromopyrimidine (1.46 g, 9.2=mmol) and K2CO3 (1.9 g, 13.7 mmol) were added. The mixture was heated to 100° C. for 18 h and at 130° C. for 48 h at which GC-MS analysis indicated some remaining starting material. The reaction mixture was cooled to room temp. and diluted with water (50 mL). The resulting solution was extracted with EtOAc (100 mL). The organic layer was washed with a saturated NaCl solution (2×50 mL), dried (MgSO4), and concentrated in vacuo. The residual solids were purified by MPLC (50% EtOAc/50% hexanes) to give the desired amine (0.650 g, 38%).
  • A13k. General Method for Substituted Aniline Formation via Nitroarene Formation Through Nucleophilic Aromatic Substitution, Followed by Reduction
  • [0209]
  • [0210]
    Step 1. 5-Bromo-2-methoxypyridine: A mixture of 2,5-dibromopyridine (5.5 g, 23.2 mmol) and NaOMe (3.76 g, 69.6 mmol) in MeOH (60 mL) was heated at 70° C. in a sealed reaction vessel for 42 h, then allowed to cool to room temp. The reaction mixture was treated with water (50 mL) and extracted with EtOAc (2×100 mL). The combined organic layers were dried (Na2SO4) and concentrated under reduced pressure to give a pale yellow, volatile oil (4.1 g, 95% yield): TLC (10% EtOAc/90% hexane) R0.57.
  • [0000]
  • [0211]
    Step 2. 5-Hydroxy-2-methoxypyridine: To a stirred solution of 5-bromo-2-methoxypyridine (8.9 g, 47.9 mmol) in THF (175 mL) at −78° C. was added an n-butyllithium solution (2.5 M in hexane; 28.7 mL, 71.8 mmol) dropwise and the resulting mixture was allowed to stir at −78° C. for 45 min. Trimethyl borate (7.06 mL 62.2 mmol) was added via syringe and the resulting mixture was stirred for an additional 2 h. The bright orange reaction mixture was warmed to 0° C. and was treated with a mixture of a 3 N NaOH solution (25 mL, 71.77 mmol) and a hydrogen peroxide solution (30%; approx. 50 mL). The resulting yellow and slightly turbid reaction mixture was warmed to room temp. for 30 min and then heated to the reflux temp. for 1 h. The reaction mixture was then allowed to cool to room temp. The aqueous layer was neutralized with a 1N HCl solution then extracted with Et2O (2×100 mL). The combined organic layers were dried (Na2SO4) and concentrated under reduced pressure to give a viscous yellow oil (3.5 g, 60%).
  • [0000]
  • [0212]
    Step 3. 4-(5-(2-Methoxy)pyridyl)oxy-1-nitrobenzene: To a stirred slurry of NaH (97%, 1.0 g, 42 mmol) in anh DMF (100 mL) was added a solution of 5-hydroxy-2-methoxypyridine (3.5 g, 28 mmol) in DMF (100 mL). The resulting mixture was allowed to stir at room temp. for 1 h, 4-fluoronitrobenzene (3 mL, 28 mmol) was added via syringe. The reaction mixture was heated to 95° C. overnight, then treated with water (25 mL) and extracted with EtOAc (2×75 mL). The organic layer was dried (MgSO4) and concentrated under reduced pressure. The residual brown oil was crystallized EtOAc/hexane) to afford yellow crystals (5.23 g, 75%).
  • [0000]
  • [0213]
    Step 4. 4-(5-(2-Methoxy)pyridyl)oxyaniline: 4-(5-(2-Methoxy)pyridyl)oxy-1-nitrobenzene was reduced to the aniline in a manner analogous to that described in Method B3d, Step 2.
  • A14a. General Method for Substituted Aniline Synthesis via Nucleophilic Aromatic Substitution using a Halopyridine
  • [0214]
  • [0215]
    3-(4-Pyridinylthio)aniline: To a solution of 3-aminothiophenol (3.8 mL, 34 mmoles) in anh DMF (90 mL) was added 4-chloropyridine hydrochloride (5.4 g, 35.6 mmoles) followed by K2CO3 (16.7 g, 121 mmoles). The reaction mixture was stirred at room temp. for 1.5 h, then diluted with EtOAc (100 mL) and water (100 mL). The aqueous layer was back-extracted with EtOAc (2×100 mL). The combined organic layers were washed with a saturated NaCl solution (100 mL), dried (MgSO4), and concentrated under reduced pressure. The residue was filtered through a pad of silica (gradient from 50% EtOAc/50% hexane to 70% EtOAc/30% hexane) and the resulting material was triturated with a Et2O/hexane solution to afford the desired product (4.6 g, 66%): TLC (100% ethyl acetate) R0.29; 1H-NMR (DMSO-d6) δ 5.41 (s, 2H), 6.64-6.74 (m, 3H), 7.01 (d, J=4.8, 2H), 7.14 (t, J=7.8 Hz, 1H), 8.32 (d, J=4.8, 2H).
  • A14b. General Method for Substituted Aniline Synthesis via Nucleophilic Aromatic Substitution using a Halopyridine
  • [0216]
  • [0217]
    4-(2-Methyl-4-pyridinyloxy)aniline: To a solution of 4-aminophenol (3.6 g, 32.8 mmol) and 4-chloropicoline (5.0 g, 39.3 mmol) in anh DMPU (50 mL) was added potassium tert-butoxide (7.4 g, 65.6 mmol) in one portion. The reaction mixture was heated at 100° C. with stirring for 18 h, then was allowed to cool to room temp. The resulting mixture was poured into water (200 mL) and extracted with EtOAc (3×150 mL). The combined extracts. were sequentially washed with water (3×100 mL) and a saturated NaCl solution (2×100 mL), dried (Na2SO4), and concentrated in vacuo. The resulting oil was purified by flash chromatography (50% EtOAc/50% hexane) to afford the desired product as a yellow oil (0.7 g, 9%): CI-MS m/z 201 ((M+H)+).
  • A14c. General Method for Substituted Aniline Synthesis via Nucleophilic Aromatic Substitution using a Halopyridine
  • [0218]
  • [0219]
    Step 1. Methyl(4-nitrophenyl)-4-pyridylamine: To a suspension of N-methyl-4-nitroaniline (2.0 g, 13.2 mmol) and K2CO3 (7.2 g, 52.2 Sol) in DMPU (30 mL) was added 4-chloropyridine hydrochloride (2.36 g, 15.77 mmol). The reaction mixture was heated at 90° C. for 20 h, then cooled to room temperature. The resulting mixture was diluted with water (100 mL) and extracted with EtOAc (100 mL). The organic layer was washed with water (100 mL), dried (Na2SO4) and concentrated under reduced pressure. The residue was purified by column chromatography (silica gel, gradient from 80% EtOAc/20% hexanes to 100% EtOAc) to afford methyl(4-nitrophenyl)-4-pyridylamine (0.42 g)
  • [0000]
  • [0220]
    Step 2. Methyl(4-aminophenyl)-4-pyridylamine: Methyl(4-nitrophenyl)-4-pyridylamine was reduced in a manner analogous to that described in Method B1.
  • A15. General Method of Substituted Aniline Synthesis via Phenol Alkylation Followed by Reduction of a Nitroarene
  • [0221]
  • [0222]
    Step 1. 4-(4-Butoxyphenyl)thio-1-nitrobenzene: To a solution of 4-(4-nitrophenyl-thio)phenol (1.50 g, 6.07 mmol) in anh DMF (75 ml) at 0° C. was added NaH (60% in mineral oil, 0.267 g, 6.67 mmol). The brown suspension was stirred at 0° C. until gas evolution stopped (15 min), then a solution of iodobutane (1.12 g, 0.690 ml, 6.07 mmol) in anh DMF (20 mL) was added dropwise over 15 min at 0° C. The reaction was stirred at room temp. for 18 h at which time TLC indicated the presence of unreacted phenol, and additional iodobutane (56 mg, 0.035 mL, 0.303 mmol, 0.05 equiv) and NaH (13 mg, 0.334 mmol) were added. The reaction was stirred an additional 6 h room temp., then was quenched by the addition of water (400 mL). The resulting mixture was extracted with Et2O (2×500 mL). The combined organics were washed with water (2×400 mL), dried (MgSO4), and concentrated under reduced pressure to give a clear yellow oil, which was purified by silica gel chromatography (gradient from 20% EtOAc/80% hexane to 50% EtOAc/50% hexane) to give the product as a yellow solid (1.24 g, 67%); TLC (20% EtOAc/80% hexane) R0.75; 1H-NMR (DMSO-d6) δ 0.92 (t, J=7.5 Hz, 3H), 1.42 (app hex, J=7.5 Hz, 2H), 1.70 (m, 2H), 4.01 (t, J=6.6 Hz, 2H), 7.08 (d, J=8.7 Hz, 2H), 7.17 (d, J=9 Hz, 2H), 7.51 (d, J=8.7 Hz, 2H), 8.09 (d, J=9 Hz, 2H).
  • [0000]
  • [0223]
    Step 2. 4-(4-Butoxyphenyl)thioaniline; 4-(4-Butoxyphenyl)thio-1-nitrobenzene was reduced to the aniline in a manner analagous to that used in the preparation of 3-(trifluoromethyl)-4-(4-pyridinylthio)aniline (Method B3b, Step 2): TLC (33% EtOAc/77% hexane) R0.38.
  • A16. General Method for Synthesis of Substituted Anilines by the Acylation of Diaminoarenes
  • [0224]
  • [0225]
    4-(4-tert-Butoxycarbamoylbenzyl)aniline: To a solution of 4,4′-methylenedianiline (3.00 g, 15.1 mmol) in anh THF (50 mL) at room temp was added a solution of di-tert-butyl dicarbonate (3.30 g, 15.1 mmol) in anh THF (10 mL). The reaction mixture was heated at the reflux temp. for 3 h, at which time TLC indicated the presence of unreacted methylenedianiline. Additional di-tert-butyl dicarbonate (0.664 g, 3.03 mmol, 0.02 equiv) was added and the reaction stirred at the reflux temp. for 16 h. The resulting mixture was diluted with Et2O (200 mL), sequentially washed with a saturated NaHCO3 solution (100 ml), water (100 mL) and a saturated NaCl solution (50 mL), dried (MgSO4), and concentrated under reduced pressure. The resulting white solid was purified by silica gel chromatography (gradient from 33% EtOAc/67% hexane to 50% EtOAc/50% hexane) to afford the desired product as a white solid (2.09 g, 46%): TLC (50% EtOAc/50% hexane) R0.45; 1H-NMR (DMSO-d6) δ 1.43 (s, 9H), 3.63 (s, 2H), 4.85 (br s, 2H), 6.44 (d, J=8.4 Hz, 2H), 6.80 (d, J=8.1 Hz, 2H), 7.00 (d, J=8.4 Hz, 2H), 7.28 (d, J=8.1 Hz, 2H), 9.18 (br s, 1H); FAB-MS m/z 298 (M+).
  • A17. General Method for the Synthesis of Aryl Amines via Electrophilic Nitration Followed by Reduction
  • [0226]
  • [0227]
    Step 1. 3-(4-Nitrobenzyl)pyridine: A solution of 3-benzylpyridine (4.0 g, 23.6 mmol) and 70% nitric acid (30 mL) was heated overnight at 50° C. The resulting mixture was allowed to cool to room temp. then poured into ice water (350 mL). The aqueous mixture then made basic with a 1N NaOH solution, then extracted with Et2O (4×100 mL). The combined extracts were sequentially washed with water (3×100 mL) and a saturated NaCl solution (2×100 mL), dried Na2SO4), and concentrated in vacuo. The residual oil was purified by MPLC (silica gel; 50% EtOAc/50% hexane) then recrystallization (EtOAc/hexane) to afford the desired product (1.0 g, 22%): GC-MS m/z 214 (M+).
  • [0000]
  • [0228]
    Step 2. 3-(4-Pyridinyl)methylaniline: 3-(4-Nitrobenzyl)pyridine was reduced to the aniline in a manner analogous to that described in Method B1
  • A18. General Method for Synthesis of Aryl Amines via Substitution with Nitrobenzyl Halides Followed by Reduction
  • [0229]
  • [0230]
    Step 1. 4-(1-Imidazolylmethyl)-1-nitrobenzene: To a solution of imidazole (0.5 g, 7.3 mmol) and 4-nitrobenzyl bromide (1.6 g, 7.3 mmol) in anh acetonitrile (30 mL) was added K2CO3 (1.0 g, 7.3 mmol). The resulting mixture was stirred at room temp. for 18 h and then poured into water (200 mL) and the resulting aqueous solution was extracted with EtOAc (3×50 mL). The combined organic layers were sequentially washed with water (3×50 mL) and a saturated NaCl solution (2×50 mL), dried (MgSO4), and concentrated in vacuo. The residual oil was purified by MPLC (silica gel; 25% EtOAc/75% hexane) to afford the desired product (1.0 g, 91%): EI-MS m/z 203 (M+).
  • [0000]
  • [0231]
    Step 2. 4-(1-Imidazolylmethyl)aniline: 4-(Imidazolylmethyl)-1-nitrobenzene was reduced to the aniline in a manner analogous to that described in Method B2.
  • A19. Formation of Substituted Hlydroxymethylanilines by Oxidation of Nitrobenzyl Compounds Followed by Reduction
  • [0232]
  • [0233]
    Step 1. 4-(1-Hydroxy-1-(4-pyridyl)methyl-1-nitrobenzene: To a stirred solution of 3-(4-nitrobenzyl)pyridine (6.0 g, 28 mmol) in CH2Cl2 (90 mL) was added m-CPBA (5.80 g, 33.6 mmol) at 10° C., and the mixture was stirred at room temp. overnight. The reaction mixture was successively washed with a 10% NaHSO3 solution (50 mL), a saturated K2CO3 solution (50 mL) and a saturated NaCl solution (50 mL), dried (MgSO4) and concentrated under reduced pressure. The resulting yellow solid (2.68 g) was dissolved in anh acetic anhydride (30 mL) and heated at the reflux temperature overnight. The mixture was concentrated under reduced pressure. The residue was dissolved in MeOH (25 mL) and treated with a 20% aqueous NH, solution (30 mL). The mixture was stirred at room temp. for 1 h, then was concentrated under reduced pressure. The residue was poured into a mixture of water (50 mL) and CH2Cl2 (50 mL). The organic layer was dried (MgSO4), concentrated under reduced pressure, and purified by column chromatography (80% EtOAc/20% hexane) to afford the desired product as a white solid. (0.53 g, 8%): mp 110-118° C.; TLC (80% EtOAc/20% hexane) R0.12; FAB-MS m/z 367 ((M+H)+, 100%).
  • [0000]
  • [0234]
    Step 2. 4-(1-Hydroxy-1-(4-pyridyl)methylaniline: 4-(1-Hydroxy-1-(4-pyridyl)-methyl-1-nitrobenzene was reduced to the aniline in a manner analogous to that described in Method B3d, Step 2.
  • A20. Formation of 2-(N-methylcarbamoyl)pyridines via the Menisci reaction
  • [0235]
  • [0236]
    Step 1. 2-(N-methylcarbamoyl)-4-chloropyridine. (Caution: this is a highly hazardous, potentially explosive reaction.) To a solution of 4-chloropyridine (10.0 g) in N-methylformamide (250 mL) under argon at ambient temp was added conc. H2SO4 (3.55 mL) (exotherm). To this was added H2O2 (17 mL, 30% wt in H2O) followed by FeSO47H2O (0.55 g) to produce an exotherm. The reaction was stirred in the dark at ambient temp for 1 h then was heated slowly over 4 h at 45° C. When bubbling subsided, the reaction was heated at 60° C. for 16 h. The opaque brown solution was diluted with H2O (700 mL) followed by a 10% NaOH solution (250 mL). The aqueous mixture was extracted with EtOAc (3×500 mL) and the organic layers were washed separately with a saturated NaCl solution (3×150 mL. The combined organics were dried (MgSO4) and filtered through a pad of silica gel eluting with EtOAc. The solvent was removed in vacuo and the brown residue was purified by silica gel chromatography (gradient from 50% EtOAc/50% hexane to 80% EtOAc/20% hexane). The resulting yellow oil crystallized at 0° C. over 72 h to give 2-(N-methylcarbamoyl)-4-chloropyridine in yield (0.61 g, 5.3%): TLC (50% EtOAc/50% hexane) R0.50; MS; 1H NMR (CDCl3): d 8.44 (d, 1H, J=5.1 Hz, CHN), 8.21 (s, 1H, CHCCO), 7.96 (b s, 1H, NH), 7.43 (dd, 1H, J=2.4, 5.4 Hz, ClCHCN), 3.04 (d, 3H, J=5.1 Hz, methyl); CI-MS m/z 171 ((M+H)+).
  • A21. General method for the Synthesis of ω-Sulfonylphenyl Anilines
  • [0237]
  • [0238]
    Step 1. 4-(4-Methylsulfonylphenoxy)-1-nitrobenzene: To a solution of 4-(4-methylthiophenoxy)-1-ntirobenzene (2 g, 7.66 mmol) in CH2Cl2 (75 mL) at 0° C. was slowly added MCPBA (57-86%, 4 g), and the reaction mixture was stirred at room temperature for 5 h. The reaction mixture was treated with a 1 N NaOH solution (25 mL). The organic layer was sequentially washed with a 1N NaOH solution (25 mL), water (25 mL) and a saturated NaCl solution (25 mL), dried (MgSO4), and concentrated under reduced pressure to give 4-(4-methylsulfonylphenoxy)-1-nitrobenzene as a solid (2.1 g).
  • [0239]
    Step 2. 4-(4-Methylsulfonylphenoxy)-1-aniline: 4-(4-Methylsulfonylphenoxy)-1-nitrobenzene was reduced to the aniline in a manner analogous to that described in Method B3d, step 2.
  • A22. General Method for Synthesis of ω-Alkoxy-ω-carboxyphenyl Anilines
  • [0240]
  • [0241]
    Step 1. 4-(3-Methoxycarbonyl-4-methoxyphenoxy)-1-nitrobenzene: To a solution of -(3-carboxy-4-hydroxyphenoxy)-1-nitrobenzene (prepared in a manner analogous to that described in Method B3a, step 1, 12 mmol) in acetone (50 mL) was added K2CO3 (5 g) and dimethyl sulfate (3.5 mL). The resulting mixture was heated at the reflux temperature overnight, then cooled to room temperature and filtered through a pad of CeliteŽ. The resulting solution was concentrated under reduced pressure, absorbed onto silica gel, and purified by column chromatography (50% EtOAc/50% hexane) to give 4-(3-methoxycarbonyl-4-methoxyphenoxy)-1-nitrobenzene as a yellow powder (3 g): mp 115 118° C.
  • [0000]
  • [0242]
    Step 2. 4-(3-Carboxy-4-methoxyphenoxy)-1-nitrobenzene: A mixture of 4-(3-methoxycarbonyl-4-methoxyphenoxy)-1-nitrobenzene (1.2 g), KOH (0.33 g), and water (5 mL) in MeOH (45 mL) was stirred at room temperature overnight and then heated at the reflux temperature for 4 h. The resulting mixture was cooled to room temperature and concentrated under reduced pressure. The residue was dissolved in water (50 mL), and the aqueous mixture was made acidic with a 1N HCl solution. The resulting mixture was extracted with EtOAc (50 mL). The organic layer was dried (MgSO4) and concentrated under reduced pressure to give 4-(3-carboxy-4-methoxyphenoxy)-1-nitrobenzene (1.04 g).
  • B. General Methods of Urea Formation B1a. General Method for the Reaction of an Aryl Amine with an Aryl Isocyanate
  • [0243]
  • [0244]
    N-(5-tert-Butyl-2-(3-tetrahydrofuranyloxy)phenyl)-N′-(4 methylphenyl)urea: To a solution of 5-tert-butyl-2-(3-tetrahydrofuranyloxy)aniline (0.078 g, 0.33 mmol) in toluene (2.0 mL) was added p-tolyl isocyanate (0.048 g, 0.36 mmol) and the resulting mixture was allowed to stir at room temp. for 8 h to produce a precipitate. The reaction mixture was filtered and the residue was sequentially washed with toluene and hexanes to give the desired urea as a white solid (0.091 g, 75%); mp 229-231° C.; 1H-NMR (DMSO-d6) δ 1.30 (s, 9H), 1.99-2.03 (m, 1H), 2.19-2.23 (m, 4H), 3.69-3.76 (m, 1H), 3.86-3.93 (m, 3H), 4.98-5.01 (m, 1H), 6.81-6.90 (m, 2H), 7.06 (d, J=8.09 Hz, 2H, 7.32 (d, J=8.09 Hz, 2H), 7.84 (s, 1H), 8.22 (d, J=2.21 Hz, 1H), 9.26 (s, 1H).
  • B1b. General Method for the Reaction of an Aryl Amine with an Aryl Isocyanate
  • [0245]
  • [0246]
    N-(2-Methoxy-5-(trifluoromethanesulfonyl)phenyl)-N′(4-methylphenyl)urea: p-Tolyl isocyanate (0.19 mL, 1.55 mmol) was added to a solution of 2-methoxy-5-(trifluoromethanesulfonyl)aniline (0.330 g, 1.29 mmol) in EtOAc (5 mL), and the reaction mixture was stirred at room temp. for 18 h. The resulting precipitate was collected by filtration and washed with Et2O to give a white solid (0.28 g). This material was then purified by HPLC (C-18 column, 50% CH3CN/50% H2O) and the resulting solids were triturated with Et2O to provide the title compound (0.198 g): 1H-NMR (CDCl3) δ 7.08 (d, J=8.5 Hz, 2H), 7.33 (d, J=8.5 Hz, 2H), 7.40 (d, J=8.8 Hz, 1H), 7.71 (dd, J=2.6, 8.8 Hz, 1H), 8.66 (s, 1H), 8.90 (d, J=2.6 Hz, 1H), 9.36 (s, 1H); FAB-MS m/z 389 ((M+1)+).
  • B1c. General Method for the Reaction of an Aryl Amine with an Aryl Isocyanate
  • [0247]
  • [0248]
    N-(2-Methoxy-5-(difluoromethanesulfonyl)phenyl)-N′-(4-methylphenyl)urea: p-Tolyl isocyanate (0.058 mL, 0.46 mmol) was added to a solution of 2-methoxy-5-(difluoromethanesulfonyl)aniline (0.100 g, 0.42 mmol) in EtOAc (0.5 mL) and the resulting mixture was stirred at room temp. for 3 d. The resulting precipitate was filtered and washed with Et2O to provide the title compound as a white solid (0.092 g): 1H-NMR (CDCl3) δ 2.22 (s, 3H) 4.01 (s, 3H), 7.02-7.36 (m, 6H), 7.54 (dd, J=2.4, 8.6 Hz, 1H), 8.57 (s, 1H), 8.79 (d, J=2.6 Hz, 1H), 9.33 (s, 1H); EI-MS m/z 370 (M+).
  • B1d. General Method for the Reaction of an Aryl Amine with an Aryl Isocyanate
  • [0249]
  • [0250]
    N-(2,4-Dimethoxy-5-(trifluoromethyl)phenyl)-N′-(4-methylphenyl)urea: p-Tolyl isocyanate (0.16 mL, 1.24 mmol) was added to a solution of 2,4-dimethoxy-5-(trifluoromethyl)aniline (0.25 g, 1.13 mmol) in EtOAc (3 mL) and the resulting mixture was stirred at room temp. for 18 h. A resulting precipitate was washed with Et2O to give the title compound as a white solid (0.36 g): 1H-NMR (CDCl3) δ 2.21 (s, 3H). 3.97 (s, 3H), 3.86 (s, 3H), 6.88 (s, 1H), 7.05 (d, J=8.5 Hz, 2H), 7.29 (d, J=8.5 Hz, 2H), 8.13 (s, 1H), 8.33 (s, 1H), 9.09 (s, 1H); FAB-MS m/z 355 ((M+1)+).
  • B1e. General Method for the Reaction of an Aryl Amine with an Aryl Isocyanate
  • [0251]
  • [0252]
    N-(3-Methoxy-2-naphthyl)-N′-(1-naphthyl)urea: To a solution of 2-amino-3-methoxynaphthalene (0.253 g, 1.50 mmol) in CH2Cl2 (3 mL) at room temp. was added a solution of 1-naphthyl isocyanate (0.247 g, 1.50 mmol) in CH2Cl2 (2 mL) and the resulting mixture was allowed to stir overnight. The resulting precipitate was separated and washed with CH2Cl2 to give the desired urea as a white powder (0.450 g, 90%): mp 235-236° C.; 1H-NMR (DMSO-d6) δ 4.04 (s, 3H), 7.28-7.32 (m, 2H), 7.38 (s, H1), 7.44-7.72 (m, 6H), 7.90-7.93 (m, 1H), 8.05-8.08 (m, 1H), 8.21-8.24 (m, 1H), 8.64 (s, 1H), 9.03 (s, 1H), 9.44 (s, 1H); FAB-MS m/z 343 ((M+H)+).
  • B1f General Method for the Reaction of an Aryl Amine with an Aryl Isocyanate
  • [0253]
  • [0254]
    N-(5-tert-Butyl-2-(2-tert-butoxycarbonyloxy)ethoxy)phenyl)-N′-(4-methylphenyl)urea: A mixture of 5-tert-butyl-2-(2-tert-butoxycarbonyloxy)ethoxy)aniline (Method A10, 0.232 g, 0.75 mmol) and p-tolyl isocyanate (0.099 mL, 0.79 mmol) in EtOAc (1 mL) was stirred at room temp. for 3 d to produce a solid, which was separated. The filtrate was purified by column chromatography (100% CHCl2) and the residue was triturated (Et2O/hexane) to give the desired product (0.262 g, 79%): mp 155-156° C.; TLC (20% EtOAc/80% hexane) R0.49; 1H-NMR (DMSO-d6) δ 1.22 (s, 9H), 1.37 (s, 9H), 2.21 (s, 3H), 4.22-4.23 (m, 2H), 4.33-4.35 (m, 2H), 6.89-7.00 (m, 4H), 7.06 (d, J=8.5 Hz, 2H), 7.32 (d, J=8.1 Hz, 2H), 7.96 (s, 1H); 8.22 (d, J=1.5 Hz, 1H), 9.22 (s, 1H); FAB-MS m/z (rel abundance) 443 ((M+H)+, 6%).
  • B2a. General Method for Reaction of an Aryl Amine with Phosgene Followed by Addition of a Second Aryl Amine
  • [0255]
  • [0256]
    N-(2-Methoxy-5-(trifluoromethyl)phenyl)-N′-(3-(4-pyridinylthio phenyl urea: To a solution of pyridine (0.61 mL, 7.5 mmol, 3.0 equiv) and phosgene (20% in toluene; 2.65 mL, 5.0 mmol, 2.0 equiv) in CH2Cl2 (20 mL) was added 2-methoxy-5-(trifluoromethyl)aniline (0.48 g, 2.5 mmol) at 0° C. The resulting mixture was allowed warm to room temp. stirred for 3 h, then treated with anh. toluene (100 mL) and concentrated under reduced pressure. The residue was suspended in a mixture of CH2Cl2 (10 mL) and anh. pyridine (10 mL) and treated with 3-(4-pyridinylthio)aniline (0.61 g, 2.5 mmol, 1.0 equiv). The mixture was stirred overnight at room temp., then poured into water (50 mL) and extracted with CH2Cl2 (3×25 mL). The combined organic layers were dried (MgSO4) and concentrated under reduced pressure. The residue was dissolved in a minimal amount of CH2Cl2 and treated with pet. ether to give the desired product as a white precipitate (0.74 g, 70%): mp 202° C.; TLC (5% acetone/95% CH2Cl2) R0.09; 1H-NMR (DMSO-d6) δ 7.06 (d, J=5.5 Hz, 2H), 7.18 (dd, J=2.4, 4.6 Hz, 2H), 7.31 (dd, J=2.2, 9.2 Hz, 1H), 7.44 (d, J=5.7 Hz, 1H), 7.45 (s, 1H), 7.79 (d, J=2.2 Hz, 1H), 8.37 (s, 2H), 8.50 (dd, J=2.2, 9.2 Hz, 2H), 9.63 (s, 1H), 9.84 (s, 1H); FAB-MS m/z 420 ((M+H)+, 70%).
  • B2b. General Method for Reaction of an Aryl Amine with Phosgene Followed by Addition of a Second Aryl Amine
  • [0257]
  • [0258]
    N-(2-Methoxy-5-(trifluoromethyl)phenyl)-N′-(4-(4-pyridinylthio)phenyl)urea: To a solution of pyridine (0.61 mL, 7.5 mmol, 3.0 equiv) and phosgene (20% in toluene; 2.65 mL, 5.0 mmol, 2.0 equiv) in CH2Cl2 (20 mL) was added 4-(4-pyridinylthio)aniline (0.506 g, 2.5 mmol) at 0° C. After stirring for 3 h at room temp., the mixture was treated with anh. toluene (100 mL) then concentrated under reduced pressure. The residue was suspended in a mixture of CH2Cl2 (10 mL) and anh. pyridine (10 mL) and treated with 2-methoxy-5-(trifluoromethyl)aniline (0.50 g, 2.5 mmol, 1.0 equiv). After stirring the mixture overnight at room temp., it was poured into a 1 N NaOH solution (50 mL) and extracted with CH2Cl2 (3×25 mL). The combined organic layers were dried (MgSO4) and concentrated under reduced pressure to give the desired urea (0.74 g, 71%): mp 215° C.; TLC (5% acetone/95% CH2Cl2) R0.08; 1H-NMR (DMSO-d6) δ 3.96 (s, 3H), 6.94 (dd, J=1.1, 4.8 Hz, 2H) 7.19 (d, J=8.4 Hz, 1H), 7.32 (dd, J=2.2, 9.3 Hz, 1H), 7.50 (d, J=8.8 Hz, 2H), 7.62 (d, J=8.8 Hz, 2H), 8.32 (d, J=5.1 Hz, 2H), 8.53 (d, J=0.7 Hz, 1H), 8.58 (s, 1H), 9.70 (s, 1H); FAB-MS m/z 420 ((M+H)+).
  • B3a. General Method for the Reaction of an Aryl Amine with Phosgene with Isolation of the Isocyanate, Followed by Reaction with a Second Aryl Amine
  • [0259]
  • [0260]
    Step 1. 5-(Difluoromethanesulfonyl)-2-methoxyphenyl isocyanate: To a solution of phosgene (1.95 M in toluene; 3.0 mL, 5.9 mmol) in CH2Cl2 (40 mL) at 0° C. was added a solution of 5-(difluoromethanesulfonyl)-2-methoxyaniline (0.70 g, 2.95 mmol) and pyridine (0.44 mL, 8.85 mmol) in CH2Cl2 (10 mL) dropwise. After being stirred at 0° C. for 30 min and at room tempt for 3 h, the reaction mixture was concentrated under reduced pressure, then treated with toluene (50 mL). The resulting mixture was concentrated under reduced pressure, then was treated with Et2O (50 mL) to produce a precipitate (pyridinium hydrochloride). The resulting filtrate was concentrated under reduced pressure to provide the title compound as a white solid (0.33 g). This material was used in the next step without further purification.
  • [0000]
  • [0261]
    Step 2. N-(2-Methoxy-5-(difluoromethanesulfonyl)phenyl)-N′-(2-fluoro-4-methylphenyl)urea: 2-Fluoro-4-methylaniline (0.022 mL, 0.19 mmol) was added to a solution of 5-(difluoromethanesulfonyl)-2-methoxyphenyl isocyanate (0.046 g, 0.17 mmol) in EtOAc (1 mL). The reaction mixture was stirred at room temp. for 3 d. The resulting precipitate was washed with Et2O to provide the title compound as a white solid (0.055 g): 1H-NMR (CDCl3) δ 2.24 (s, 3H), 4.01 (s, 3H), 6.93 (d, J=8.5 Hz, 3H), 7.01-7.36 (m, 3H), 7.56 (dd, J=2.4, 8.6 Hz, 1H), 7.98 (app t, J=8.6 Hz, 1H), 8.79 (d, J=2.2 Hz, 1H), 9.07 (s, 1H), 9.26 (s, 1H); FAB-MS m/z 389 ((M+1)+).
  • B3b. General Method for the Reaction of an Aryl Amine with Phosgene with Isolation of the Isocyanate, Followed by Reaction with a Second Aryl Amine
  • [0262]
  • [0263]
    Step 1. 2-Methoxy-5-trifluoromethylphenyl Isocyanate: To a solution of phosgene (1.93 M in toluene; 16 mL, 31.4 mmol) in CH2Cl2 (120 mL) at 0° C. was added a solution of 2-methoxy-5-(trifluoromethyl)aniline (3.0 g, 15.7 mmol) and pyridine (2.3 mL, 47.1 mmol) in CH2Cl2 (30 mL) dropwise. The resulting mixture was stirred at 0 t C for 30 min and at room temp for 3 h, then concentrated under reduced pressure. The residue was diluted with toluene (30 mL), concentrated under reduced pressure, and treated with Et2O. The resulting precipitate (pyridinium hydrochloride) was removed and the filtrate, was concentrated under reduced pressure to give the title compound as a yellow oil (3.0 g) which crystallized upon standing at room temp. for a few days.
  • [0000]
  • [0264]
    Step 2. N-(2-Methoxy-5-(trifluoromethyl)phenyl)-N′-(4-fluorophenyl)urea: 4-Fluoroaniline (0.24 mL, 2.53 mmol) was added to a solution of 2-methoxy-5-(trifluoromethyl)phenyl isocyanate (0.50 g, 2.30 mmol) in EtOAc (6 mL) and the reaction mixture was stirred at room temp. for 3 d. The resulting precipitate was washed with Et2O to give the title compound as a white solid (0.60 g): NMR: 3.94 (s, 3H). 7.13-7.18 (m, 3H), 7.30 (dd, J=1.5, 8.4 Hz, 1H), 7.44 (m, 2H), 8.45 (s, 1H), 8.52 (d, J=2.2 Hz, 1H), 9.42 (s, 1H); FAB-MS m/z 329 ((M+1)+).
  • B4. General Method for Urea Formation via Curtius Rearrangement, Followed by Trapping with an Amine
  • [0265]
  • [0266]
    N-(3-Methoxy-2-naphthyl)-N′-(4-methylphenyl)urea: To a solution of 3-methoxy-2-naphthoic acid (Method A6, Step 2; 0.762 g, 3.80 mmol) and Et3N (0.588 mL, 4.2 mmol) in anh toluene (20 mL) at room temp. was added a solution of diphenylphosphoryl azide (1.16 g, 4.2 mmol) in toluene (5 mL). The resulting mixture was heated to 80° C. for 2 h, cooled to room temp., and p-toluidine (0.455 g, 4.1 mmol) was added. The mixture was heated at 80° C. overnight, cooled to room temp., quenched with a 10% citric acid solution, and extracted with EtOAc (2×25 mL). The combined organic layers were washed with a saturated NaCl solution (25 mL), dried (MgSO4), and concentrated in vacuo. The residue was triturated with CH2Cl2 to give the desired urea as white powder (0.700 g, 61%): mp 171-172° C.; 1H-NMR (DMSO-d6) δ 2.22 (s, 3H), 3.99 (s, 3H), 7.07 (d, J=8.49 Hz, 2H), 7.27-7.36 (m, 5H), 7.67-7.72 (m, 2H), 8.43 (s, 1H), 8.57 (s, 1H), 9.33 (s, 1H); FAB-MS m/z 307 ((M+H)+).
  • B5. General Method for the Reaction of Substituted Aniline with N,N′-Carbonyldiimidazole Followed by Reaction with a Second Amine
  • [0267]
  • [0268]
    N-(5-Chloro-2-hydroxy-4-nitrophenyl)-N′-(4-(4-pyridinylmethyl)phenyl)urea: A solution of 4-(4-pyridinylmethyl)aniline (0.300 g, 1.63 mmol) and N,N′-carbonyldiimidazole (0.268 g, 1.65 mmol) in CH2Cl2 (10 mL) was stirred at room temp. for 1 h at which time TLC analysis indicated no starting aniline. The reaction mixture was then treated with 2-amino-4-chloro-5-nitrophenol (0.318 g, 1.65 mmol) and stirred at 40-45° C. for 48 h. The resulting mixture was cooled to room temp. and diluted with EtOAc (25 mL). The resulting precipitate was separated to give the desired product (0.416 g, 64%): TLC (50% acetone/50% CH2Cl2) R0.40; 1H-NMR (DMSO-d6) δ 3.90 (s, 2H), 7.18 (d, J=8.4 Hz, 2H), 7.21 (d, J=6 Hz, 2H), 7.38 (d, J=8.4 Hz, 2H), 7.54 (s, 1H), 8.43-8.45 (m, 3H), 8.78 (s, 1H), 9.56 (s, 1H), 11.8 (br s, 1H); FAB-MS m/z (rel abundance) 399 ((M+H)+, 10%).
  • B6. General Method for the Synthesis of Symmetrical Diphenyl Ureas as Side-Products of Urea Forming reactions
  • [0269]
  • [0270]
    Bis(4-chloro-3-(trifluoromethyl)phenyl)urea: To a solution of 5-amino-3-tert-butylisoxazole (0.100 g) in anh toluene (5 mL) was added 4-chloro-3-(trifluoromethyl)phenyl isocyanate (0.395 g). The reaction vessel was sealed, heated at 85° C. for 24 h, and cooled to room temp. The reaction mixture was added to a slurry of DowexŽ 50WX2-100 resin (0.5 g) in CH2Cl2 (40 mL), and the resulting mixture was stirred vigorously for 72 h. The mixture was filtered and the filtrate was concentrated under reduced pressure. The residue was purified by column chromatography (gradient form 100% CH2Cl2 to 5% MeOH/95% CH2Cl2) to give bis(4-chloro-3-(trifluoromethyl)phenyl)urea followed by N-(3-tert-butyl-5-isoxazolyl)-N′-(4-chloro-3-(trifluoromethyl)phenyl)urea. The residue from the symmetrical urea fractions was triturated (Et2O/hexane) to give the urea as a white solid (0.110 g): TLC (3% MeOH/97% CH2Cl2) R0.55; FAB-MS m/z 417 ((M+H)+).
  • C. Urea Interconversions and Misc. Reactions C1. General Method for Alkylation of Hydroxyphenyl Ureas
  • [0271]
  • [0272]
    Step 1. N-(2-Hydroxy-5-(trifluoromethylthio)phenyl)-N′-(4-methylphenyl)urea: p-Tolyl isocyanate (0.066 mL, 0.52 mmol) was added to a solution of 2-hydroxy-5-(trifluoromethylthio)aniline (0.100 g, 0.48 mmol) in EtOAc (2 mL) and the reaction mixture was stirred at room temp. for 2 d. The resulting precipitate was washed with EtOAc to provide the title compound (0.13 g): 1H-NMR (CDCl3) δ 2.24 (s, 3H). 7.44-7.03 (m, 6H), 8.46 (s, 1H), 8.60 (d, J=1.8 Hz, 1H), 9.16 (s, 1H), 10.41 (s, 1H); FAB-MS m/z 343 ((M+1)+). This material was used in the next step without purification.
  • [0000]
  • [0273]
    Step 2. N-(2-Methoxy-5-(trifluoromethylthio)phenyl)-N′-(4-methylphenyl)urea: A solution of N-(2-hydroxy-5-(trifluoromethylthio)phenyl)-N′-(4-methylphenyl)urea (0.125 g, 0.36 mmol), iodomethane (0.045 mL, 0.73 mmol), and K2CO (100 mg, 0.73 mmol) in acetone (2 mL) was heated at the reflux temp. for 6 h, then was cooled to room temp. and concentrated under reduced pressure. The residue was dissolved in a minimal amount of MeOH, absorbed onto silica gel, and then purified by flash chromatography (3% Et2O/97% CH2Cl2) to provide the title compound as a white solid (68 mg): 1H-NMR (CDCl3) δ 2.22 (s, 3H), 3.92 (s, 3H), 7.05-7.32 (m, 6H), 8.37 (s, 1H), 8.52 (d, J=2.2 Hz, 1H), 9.27 (s, 1H); FAB-MS m/z 357 ((M+1)+).
  • C2. General Method for the Reduction of Nitro-Containing Ureas
  • [0274]
  • [0275]
    N-(5-tert-Butyl-2-methoxyphenyl)-N′-(2-amino-4-methylphenyl)urea: A solution of N-(5-tert-butyl-2-methoxyphenyl)-N′-(2-nitro-4-methylphenyl)urea (prepared in a manner analogous to Method B1a; 4.0 g, 11.2 mmol) in EtOH (100 mL) was added to a slur of 10% Pd/C (0.40 g) in EtOH (10 mL), and the resulting mixture was stirred under an atmosphere of H2 (balloon) at room temp. for 18 h. The mixture was filtered through a pad of CeliteŽ and concentrated in vacuo to afford the desired product (3.42 g, 94%) as a powder: mp 165-166° C.; 1H-NMR (DMSO-d6) δ 1.30 (s, 9H), 2.26 (s, 3H), 3.50 (br s, 2H), 3.71 (s, 3H), 6.39 (br s, 1H), 6.62 (s, 1H), 6.73 (d, J=8.46 Hz, 1H), 6.99 (dd, J=2.21, 8.46 Hz, 1H), 7.05 (d, J=8.46 Hz, 1H), 7.29 (s, 1H), 8.22 (d, J=2.57 Hz, 1H; FAB-MS m/z 328 ((M+H)+).
  • C3. General Method of Thiourea Formation by Reaction with a Thioisocyanate
  • [0276]
  • [0277]
    N-(5-tert-Butyl-2-methoxyphenyl)-N′-(1-naphthyl)thiourea: To a solution of 5-tert-butyl-2-methoxyaniline (0.372 g, 2.07 mmol) in toluene (5 mL) was added 1-naphthyl thioisocyanate (0.384 g, 2.07 mmol) and the resulting mixture was allowed to stir at room temp. for 8 h to produce a precipitate. The solids were separated and sequentially washed with toluene and hexane to give the desired product as an off-white powder (0.364 g, 48%): mp 158-160° C.; 1H-NMR (DMSO-d6) δ 1.31 (s, 91), 3.59 (s, 3H), 6.74 (d, J=8.46 Hz, 1H), 7.13 (dd, J=2.21, 8.46 Hz, 1H), 7.53-7.62 (m, 4H), 7.88-7.95 (m, 4H), 8.06-8.08 (m, 1H), 8.09 (br s, 1H); FAB-MS m/z 365 ((M+H)+).
  • C4. General Method for Deprotection of tert-Butyl Carbonate-Containing Ureas
  • [0278]
  • [0279]
    N-(5-tert-Butyl-2-(2-hydroxyethoxy)phenyl)-N′-(4-methylphenyl)urea: A solution of N-(5-tert-butyl-2-(2-tert-butoxycarbonyloxy)ethoxy)phenyl)-N′-(4-methylphenyl)urea (Method B1f 0.237 g, 0.54 mmol) and TFA (0.21 mL, 2.7 mmol) in CH2Cl2 (2 mL) was stirred at room temp for 18 h, then was washed with a saturated NaHCO3 solution (2 mL). The organic layer was dried by passing through 1PS filter paper (WhatmanŽ) and concentrated under reduced pressure. The resulting white foam was triturated (Et2O/hexane), then recrystallized (Et2O) to give the desired product (3.7 mg): TLC (50% EtOAc/50% hexane) R0.62; 1H-NMR (DMSO-d6) δ 1.22 (s, 9H), 3.75-3.76 (m, 2H), 4.00-4.03 (m, 2H), 4.80 (t, J=5.0 Hz, 1H), 6.88-6.89 (m, 4H), 7.06 (d, J=8.5 Hz, 2H), 7.33 (d, J=8.1 Hz, 2H), 7.97 (s, 1H), 8.20 br s, 1H), 9.14 (s, 1H); FAB-MS m/z (rel abundance) 343 ((M+H)+, 100%).
  • [0280]
    The following compounds have been synthesized according to the General Methods listed above:
  • [0000]
    TABLE 1
    2-Substituted-5-tert-butylphenyl Ureas
    mp TLC Solvent Mass Synth.
    Example R1 R2 (° C.) Rf System Spec. Source Method
    1 OH 0.54 2%MeOH/98%CH2Cl2 299(M + H)+ FAB B1d
    2 OMe 199-200 313(M + H)+ FAB B1d
    3 OMe 208-209 390(M+) EI B1d
    4 OMe 192-194 389(M + H)+ FAB B1d
    5 OMe 0.58 50%EtOAc/50%hexane 347(M + H)+ FAB B3b
    6 OMe 0.62 50%EtOAc/50%hexane 351(M + H)+ FAB B3b
    7 OMe 0.71 50%EtOAc/50%hexane 331(M + H)+ FAB B1d
    8 OMe 0.74 50%EtOAc/50%hexane 331(M + H)+ FAB B3b
    9 OMe 0.66 20%EtOAc/80%hexane 327(M + H)+ FAB B1d
    10 OMe 0.62 20%EtOAc/80%hexane 331(M + H)+ FAB B1d
    11 OMe 0.42 13%EtOAc/87%hexane 335(M + H)+ FAB B1d
    12 OMe 0.52 2%MeOH/98%CH2Cl2 327(M + H)+ FAB B1d
    13 OMe 0.56 2%MeOH/98%CH2Cl2 335(M + H)+ FAB B1d
    14 OMe 0.48 2%MeOH/98%CH2Cl2 351(M + H)+ FAB B1d
    15 OMe 0.50 2%MeOH/98%CH2Cl2 347(M + H)+ FAB B1d
    16 OMe 201-202 390(M + H)+ FAB B2a
    17 OMe 199-200 390(M + H)+ FAB B2a
    18 OMe 198-199 0.45 25%EtOAc/75%hexane B1a
    19 OMe 181-182 389(M + H)+ CI B2a
    20 OMe 181-183 390(M+) EI B1a
    21 OMe 175-177 358(M + H)+ FAB B1a
    22 OMe 219-220 358(M + H)+ FAB B1a
    23 OMe 165-166 328(M + H)+ FAB C2
    24 OMe 102-104 271(M + H)+ FAB C2
    25 OMe 236-238 349(M + H)+ FAB B1a
    26 OMe 192-194 367(M + H)+ FAB B1a
    27 OMe 137-140 550(M + H)+ FAB B2a
    28 OMe 197-199 434(M + H)+ CI A8, B2a
    29 OMe 212-215 416(M + H)+ FAB B2a
    30 OMe 195 405(M + H)+ FAB B1a
    31 OMe 110 0.07 5%acetone/95%CH2Cl2 408(M + H)+ FAB B2b
    32 OMe 185 0.67 5%acetone/95%CH2Cl2 425(M + H)+ FAB B2a
    33 OMe 214-215 0.54 5%acetone/95%CH2Cl2 448(M + H)+ FAB B2a
    34 OMe 180 0.56 5%acetone/95%CH2Cl2 421(M + H)+ FAB B2a
    35 0.67 50%EtOAc/50%hexane 343(M + H)+ FAB A10, B1f,C4
    36 0.45 50%EtOAc/50%hexane 340(M + H)+ FAB B1d
    37 222-223 354(M + H)+ ES B1c
    38 203-205 366(M + H)+ FAB B1d
    39 230-232 367(M + H)+ FAB B1d
    40 197-198 406(M + H)+ FAB A9, B1a
    41 204-205 392(M + H)+ FAB A9, B1a
    42 217-218 424(M + H)+ FAB A9, B1a
    43 187-188 370(M + H)+ FAB A9, B1a
    44 118-120 462(M + H)+ FAB A9, B1a
    45 146-148 448(M + H)+ FAB A9, B1a
    46 110-113 480(M + H)+ FAB A9, B1a
    47 95-100 400(M + H)+ FAB A9, B1a
    48 107-110 398(M + H)+ FAB A9, B1a
    49 180-182 472(M + H)+ FAB A9, B1a
    50 217-219 388(M + H)+ FAB A9, B1a
    51 116-120 420(M + H)+ FAB A9, B1a
    52 100-105 406(M + H)+ FAB A9, B1a
    53 103-105 438(M + H)+ FAB A9, B1a
    54 118-120 384(M + H)+ FAB A9, B1a
    55 125-128 394(M + H)+ FAB A1, B1a
    56 227-230 468(M + H)+ FAB A1, B1a
    57 154-156 434(M + H)+ FAB A1, B1a
    58 169-171 373(M + H)+ FAB A2, B1a
    59 157-159 423(M + H)+ FAB A2, B1a
    60 229-231 369(M + H)+ FAB A2, B1a
    61 200-204 468(M + H)+ FAB B2a
    62 187-188 508(M + H)+ FAB B2a
    63 204-206 413(M + H)+ FAB B1a
    64 192-194 389(M + H)+ FAB A7, B1a
    65 183-185 425(M + H)+ FAB A7, B1a
    66 159-160 443(M + H)+ FAB A7, B1a
    67 179-180 411(M + H)+ FAB A7, B1a
    68 0.06 10%EtOAc/90%hexane 408(M + H)+ FAB A7, B1a
    69 227-229 377(M + H)+ FAB A7, B1a
    70 216-217 381(M + H)+ FAB A7, B1a
    71 213-214 431(M + H)+ FAB A7, R1a
    72 200-201 399(M + H)+ FAB A7, B1a
    73 134-136 443(M+) EI A7, B1a
    74 185-186 459(M + H)+ FAB A7, B1a
    75 207-208 419(M + H)+ FAB A7, B1a
  • [0000]
    TABLE 2
    2-Substituted-5-(trifluoromethyl)phenyl Ureas
    mp TLC Solvent Mass Synth.
    Example R1 R2 (° C.) Rf System Spec. Source Method
    76 OMe 185-186 325(M + H)+ FAB B1d
    77 OMe 0.22 20%EtOAc/80%hexane 329(M + H)+ FAB B3b
    78 OMe 0.49 20%EtOAc/80%hexane 343(M + H)+ FAB B3b
    79 OMe 0.32 20%EtOAc/80%hexane 343(M + H)+ FAB B3b
    80 OMe 0.37 20%EtOAc/80%hexane 359(M + H)+ FAB B3b
    81 OMe 0.44 20%EtOAc/80%hexane 363(M + H)+ FAB B3b
    82 OMe 0.68 50%EtOAc/50%hexane 339(M + H)+ FAB B1d
    83 OMe 0.68 50%EtOAc/50%hexane 343(M + H)+ FAB B1d
    84 OMe 0.60 50%EtOAc/50%hexane 347(M + H)+ FAB B1d
    85 OMe 0.53 2%MeOH/98%CH2Cl2 339(M + H)+ FAB B1d
    86 OMe 0.29 2%MeOH/98%CH2Cl2 347(M + H)+ FAB B1d
    87 OMe 0.27 2%MeOH/98%CH2Cl2 363(M + H)+ FAB B1d
    88 OMe 0.45 2%MeOH/98%CH2Cl2 359(M + H)+ FAB B1d
    89 OMe 184-185 401(M + H)+ FAB B2a
    90 OMe 176-178 402(M +) FAB B21
    91 OMe 231-233 361(M + H)+ FAB B1a
    92 OMe 192-194 379(M + H)+ FAB B1a
    93 OMe 198 417(M + H)+ FAB B1e
    94 OMe 206 0.58 5%acetone/95%CH2Cl2 437(M + H)+ FAB B2a
    95 OMe 98-99 0.50 5%acetone/95%CH2Cl2 B2a
    96 OMe 190 0.65 5%acetone/95%CH2Cl2 B2a
    97 OMe 194 0.76 5%acetone/95%CH2Cl2 464(M + H)+ FAB B2a
    98 OMe 210-211 0.07 5%acetone/95%CH2Cl2 402(M + H)+ FAB B2a
    99 OMe 202 0.09 5%acetone/95%CH2Cl2 420(M + H)+ FAB B2a
    100 OMe 215 0.08 5%acetone/95%CH2Cl2 420(M + H)+ FAB B2a
    101 OMe 206 0.05 5%acetone/95%CH2Cl2 404(M + H)+ FAB B2a
    102 OMe 0.78 5%acetone/95%CH2Cl2 471(M + H)+ FAB B1a
    103 OMe 471(M + H)+ FAB B1a
    104 OMe 487(M + H)+ FAB B1a
    105 0.65 20%EtOAc/80%hexane 352(M + H)+ FAB B1d
    106 159-160 0.33 25%EtOAc/75%hexane 353(M + H)+ FAB A5, B1a
    107 152-153 0.35 25%EtOAc/75%hexane 339(M + H)+ FAB A5, B1a
    108 SMe 246-247 0.30 25%EtOAc/75%hexane 377(M + H)+ FAB B1a
    109 SMe 210-211 0.35 25%EtOAc/75%hexane 345(M + H)+ CI B1a
    110 SMe 195-196 0.35 25%EtOAc/75%hexane 314(M + H)+ FAB B1a
    111 SMe 196-197 0.40 25%EtOAc/75%hexane 395(M + H)+ FAB B1a
  • [0000]
    TABLE 3
    S-Substituted 2-Methoxy-5-sulfonylphenyl Ureas
    mp TLC Solvent Mass Synth.
    Example R2 R3 (° C.) Rf System Spec. Source Method
    112 F 205-207 339(M + H)+ HPLCES-MS B1d
    113 CHF2 195-196 370(M+) EI B1d
    114 CHF2 0.46 50%EtOAc/50%hexane 389(M + H)+ FAB B3a
    115 CHF2 0.21 50%EtOAc/50%hexane 405(M + H)+ FAB B3a
    116 CHF2 0.23 20%EtOAc/80%hexane 409(M + H)+ FAB B3a
    117 CHF2 0.40 50%EtOAc/50%hexane 389(M + H)+ FAB B3a
    118 CHF2 0.53 50%EtOAc/50%hexane 375(M + H)+ FAB B3a
    119 CHF2 0.58 50%EtOAc/50%hexane 389(M + H)+ FAB R1c
    120 CHF2 0.48 50%EtOAc/50%hexane 389(M + H)+ FAB B1d
    121 CHF2 0.44 50%EtOAc/50%hexane 393(M + H)+ FAB B1c
    122 CHF2 0.33 5%MeOH/95%CH2Cl2 385(M + H)+ FAB B1c
    123 CHF2 393(M + H)+ FAB B1c
    124 CHF2 409(M + H)+ FAB B1c
    125 CHF2 405(M + H)+ FAB B1c
    126 CHF2 0.56 50%EtOAc/50%hexane 385(M + H)+ FAB B1c
    127 CF3 0.56 50%EtOAc/50%hexane 389(M + H)+ FAB A3, B1d
  • [0000]
    TABLE 4
    3-Substituted-2-naphthyl Ureas
    mp TLC Solvent Mass Synth.
    Example R1 R2 (° C.) Rf System Spec. Source Method
    128 OMe 171-172 0.40 25%EtOAc/75%hexane 307(M + H)+ FAB B4
    129 OMe 197-199 0.40 14%EtOAc/86%hexane 325(M + H)+ FAB B4
    130 OMe 235-236 0.45 25%EtOAc/75%hexane 343(M + H)+ FAB A6, B1a
    131 OMe 236-237 0.45 25%EtOAc/75%hexane 311(M + H)+ FAB A6, B1a
    132 OMe 209-211 311(M + H)+ FAB A6, B1a
    133 OMe 225-226 321(M + H)+ FAB A6, B1a
    134 OMe 199-200 395(M + H)+ FAB A6, B1a
    135 OMe 227-228 361(M + H)+ FAB A6, B1a
    136 OMe 207-208 327(M + H)+ FAB A6, B1a
    137 OMe 234-235 361(M + H)+ FAB A6, B1a
    138 OMe 228-229 352(M + H)+ FAB A6, B1a
    139 OMe 190-195 323(M + H)+ FAB A6, B1a
    140 OMe 203-205 310(M + H)+ FAB A6, B1a
    141 OMe 209-210 307(M + H)+ FAB A6, B1a
    142 OMe 200-201 323(M + H)+ FAB A6, B1a
    143 OMe 201-202 307(M + H)+ FAB A6, B1a
    144 OMe 216-218 385(M + H)+ FAB A6, B1a
    145 OMe 181-182 361(M + H)+ FAB A6, B1a
    146 OMe 238-239 0.25 25%EtOAc/75%hexane 402(M + H)+ FAB B4
    147 OMe 199-200 0.20 25%EtOAc/75%hexane 384(M + H)+ FAB B4
    148 OMe 175-176 321(M + H)+ FAB A6, B1a
    149 OMe 164-166 544(M + H)+ FAB A6, B1a
    150 OMe 206-209 446(M + H)+ FAB A6, B1a
    151 OMe 234-237 410(M + H)+ FAB B2a
    152 OMe 209-211 0.40 25%EtOAc/75%hexane 414(M+) EI B4
  • [0000]
    TABLE 5
    Misc. Ureas
    mp TLC Solvent Mass Synth.
    Example R2 (° C.) Rf System Spec. Source Method
    153 183-184 327(M + H)+ FAB B1d
    154 156-157 312(M+) EI B1d
    155 0.46 50%EtOAc/50%hexane 291(M + H)+ FAB B1d
    156
    157 0.40 50%acetone/50%CH2Cl2 399(M + H)+ FAB B5
    158 219-221 336(M + H)+ FAB B1d
    159 204-205 305(M + H)+ FAB B1d
    160 208-210 302(M + H)+ FAB B1d
    161 226-228 355(M + H)+ FAB B1d
    162 160-162 328(M + H)+ FAB B1a
    163 0.85 50%EtOAc/50%hexane 291(M + H)+ FAB B1b
    164 225-226 0.60 25%EtOAc/75%hexane 367(M + H)+ FAB A4, B1a
    165 0.55 3%MeOH/97%CH2Cl2 417(M + H)+ FAB B6
    166 169-171 407(M + H)+ FAB B1a
    167 158-160 C3 365(M + H)+ FAB C3
  • Biological Examples P38 Kinase Assay
  • [0281]
    The in vitro inhibitory properties of compounds were determined using a p38 kinase inhibition assay. P38 activity was detected using an in vitro kinase assay run in 96-well microtiter plates. Recombinant human p38 (0.5 μg/mL) was mixed with substrate (myelin basic protein, 5 μg/mL) in kinase buffer (25 mM Hepes, 20 mM MgCl2 and 150 mM NaCl) and compound. One μCi/well of 33P-labeled ATP (10 μM) was added to a final volume of 100 μL. The reaction was run at 32° C. for 30 min. and stopped with a 1M HCl solution. The amount of radioactivity incorporated into the substrate was determined by trapping the labeled substrate onto negatively charged glass fiber filter paper using a 1% phosphoric acid solution and read with a scintillation counter. Negative controls include substrate plus ATP alone.
  • [0282]
    All compounds exemplified displayed p38 IC50s of between 1 nM and 10 μM.
  • LPS Induced TNFα Production in Mice
  • [0283]
    The in vivo inhibitory properties of selected compounds were determined using a murine LPS induced TNFα production in vivo model. BALB/c mice (Charles River Breeding Laboratories; Kingston, N.Y.) in groups of ten were treated with either vehicle or compound by the route noted. After one hour, endotoxin (E. coli lipopolysaccharide (LPS) 100 μg) was administered intraperitoneally (i.p.). After 90 min, animals were euthanized by carbon dioxide asphyxiation and plasma was obtained from individual animals by cardiac puncture into heparinized tubes. The samples were clarified by centrifugation at 12,500×g for 5 min at 4° C. The supernatants were decanted to new tubes, which were stored as needed at −20° C. TNFα levels in sera were measured using a commercial murine TNF ELISA kit (Genzyme).
  • [0284]
    The proceeding examples can be repeated with similar success by substituting the generically of specifically described reactants and/or operating conditions of this invention for those used in the proceeding examples
  • [0285]
    From the foregoing discussion, one skilled in the art can easily ascertain the essential characteristics of this invention and, without departing from the spirit and scope thereof can make various changes and modifications of the invention to adapt it to various usages and conditions.
Patent Citations
Cited PatentFiling datePublication dateApplicantTitle
US502504 *Nov 18, 1892Aug 1, 1893 Hermann thoms
US1792156 *Jan 5, 1929Feb 10, 1931Gen Aniline Works Inc5-halogen-2-amino-1-alkyloxy and 1-aralkyloxy-benzenes and intermediate products thereof and process of preparing them
US2046375 *May 24, 1932Jul 7, 1936Ici Ltdp-halogen-omicron-alkoxy-aniline derivatives and process of preparing the same
US2093265 *Mar 26, 1932Sep 14, 1937Ici LtdProcess for the manufacture of diaryl ureas
US2288422 *Nov 13, 1939Jun 30, 1942Gen Aniline & Film CorpMixed ureas
US2649476 *Apr 24, 1951Aug 18, 1953Variapat AgTrifluoromethylated diphenyl ether sulfonic acids
US2683082 *Jan 26, 1952Jul 6, 1954Ethyl CorpNu-aryl-nu'-(p-hydroxyphenyl) ureas as antioxidants for petroleum hydrocarbon fuels
US2745874 *Jun 16, 1954May 15, 1956Geigy Ag J RInsecticidal derivatives of diphenyl urea
US2781330 *Feb 9, 1953Feb 12, 1957Monsanto ChemicalsRubber containing urea compound as an anti-exposure cracking agent
US2797214 *Feb 15, 1954Jun 25, 1957Geigy Ag J RTetrakisazo dyestuffs
US2867659 *Aug 16, 1956Jan 6, 1959Geigy Ag J RPolyhalogen substituted monohydroxydiphenyl urea and thiourea compounds
US2877268 *Dec 24, 1956Mar 10, 1959Monsanto ChemicalsSubstituted ureas
US2973386 *Jan 5, 1943Feb 28, 1961Harry A WeldonPurification of sym dichloro-bis (2, 4, 6-trichlorophenyl)urea
US3200035 *Jun 4, 1962Aug 10, 1965Ciba LtdTreatment of synthetic products, especially synthetic fibers
US3230141 *Aug 12, 1960Jan 18, 1966Geigy Ag J RMethod for protecting fibers against attack by insects and bacteria with diphenyl urea compositions
US3424760 *Mar 7, 1966Jan 28, 1969Robins Co Inc A H3-ureidopyrrolidines
US3424761 *Mar 7, 1966Jan 28, 1969Robins Co Inc A H3-ureidopyrrolidines
US3424762 *Mar 7, 1966Jan 28, 1969Robins Co Inc A HCertain 3-ureidopyrrolidines
US3646059 *May 5, 1969Feb 29, 1972Du PontPlant growth regulatory ureidopyrazoles
US3743498 *Aug 14, 1970Jul 3, 1973Du PontMethod of selectively controlling undesirable vegetation
US3754887 *Feb 25, 1972Aug 28, 1973Du PontUreidopyrazoles defoliants
US3823161 *May 7, 1970Jul 9, 1974Exxon Research Engineering CoAminothiophene derivatives
US3828001 *Aug 13, 1970Aug 6, 1974May & Baker LtdThiophene derivatives
US3860645 *May 23, 1973Jan 14, 1975Givaudan CorpBacteriostatic substituted carbanilides
US3931201 *Jan 22, 1974Jan 6, 1976The Dow Chemical CompanySubstituted pyridinyloxy(thio)phenyl -acetamides, -ureas and urea derivatives
US4001256 *Jun 25, 1975Jan 4, 1977The Upjohn CompanyPyridylalkyl phenyl ureas and their n-oxides
US4009847 *Mar 11, 1975Mar 1, 1977E. I. Du Pont De Nemours And Company1-Tertiary-alkyl-3-(substituted thienyl)ureas and 1-tertiary-alkyl-3-(substituted thietyl)ureas as antihypertensive agents
US4042372 *Nov 19, 1976Aug 16, 1977Eli Lilly And CompanySubstituted thiadiazolotriazinediones and method of preparation
US4071524 *Nov 8, 1976Jan 31, 1978Riker Laboratories, Inc.Derivatives of urea
US4183854 *Jul 28, 1978Jan 15, 1980John Wyeth & Brother LimitedThiazole compound
US4212981 *Nov 16, 1977Jul 15, 1980Shionogi & Co., Ltd.Process for preparing 3-isoxazolylurea derivatives
US4279639 *Aug 1, 1979Jul 21, 1981Toshihiko OkamotoN-(2-Substituted-4-pyridyl)ureas and thioureas as well as plant growth regulators containing same, and method for using compounds as plant growth regulators
US4437878 *Mar 31, 1983Mar 20, 1984Basf AktiengesellschaftDihydrothiophenecarboxylates and their use for controlling undersirable plant growth
US4468380 *May 6, 1981Aug 28, 1984Eli Lilly And CompanyAnticoccidial combinations comprising polyether antibiotics and carbanilides
US4511571 *Oct 12, 1982Apr 16, 1985Ciba Geigy CorporationN-(2-Pyridyloxyphenyl)-N'-benzoyl ureas, pesticidal compositions containing same and pesticidal methods of use
US4514571 *May 19, 1983Apr 30, 1985Ube Industries, Ltd.Process for the preparation of urea derivatives
US4526997 *May 18, 1984Jul 2, 1985Doherty George O P OAnticoccidial combinations comprising polyether antibiotics and carbanilides
US4643849 *Nov 14, 1983Feb 17, 1987Toyama Chemical Co., Ltd.Intermediates for urea and thiourea derivatives
US4740520 *Nov 14, 1986Apr 26, 1988Bayer AktiengesellschaftUse of thienylurea derivatives as selective fungicides
US4760063 *Nov 12, 1986Jul 26, 1988Bayer AktiengsellschaftThienooxazinones, processes for their preparation, and their use as growth promoters
US4808588 *Jul 30, 1987Feb 28, 1989Beecham Group, P.L.C.Heterocyclic ureas and carbonates useful as pharmaceuticals
US4820871 *Oct 7, 1987Apr 11, 1989Bayer AktiengesellschaftProcess for the preparation of N,N-diaryl-ureas
US4983605 *Oct 20, 1987Jan 8, 1991Ishihara Sangyo Kaisha Ltd.Pharmaceutical composition
US4985449 *Jun 13, 1989Jan 15, 1991Ishihara Sangyo Kaisha Ltd.N-benzoyl-N-pyridyloxy phenyl urea compounds and pesticide compositions containing them
US5036072 *Jan 23, 1990Jul 30, 1991Ishihara Sangyo Kaisha Ltd.Antiviral agent
US5098907 *Jan 23, 1990Mar 24, 1992Ishihara Sangyo Kaisha Ltd.Powdery pharmaceutical composition containing benzoyl urea, a dispersant and silicic acid
US5130331 *Oct 9, 1990Jul 14, 1992Ciba-Geigy CorporationThienylthioureas, -isothioureas and -carbodiimides
US5185358 *Jun 24, 1991Feb 9, 1993Warner-Lambert Co.3-heteroatom containing urea and thiourea ACAT inhibitors
US5312820 *Jul 17, 1992May 17, 1994Merck & Co., Inc.Substituted carbamoyl and oxycarbonyl derivatives of biphenylmethylamines
US5319099 *Jan 14, 1992Jun 7, 1994Shionogi Seiyaku Kabushiki Kaisha3-benzylidene-1-carbamoyl-2-pyrrolidone compounds useful as antiinflammatory agents
US5399566 *Jun 19, 1991Mar 21, 1995Meiji Seika Kabushiki KaishaPyridine derivatives having angiotensin II antagonism
US5423905 *Jul 18, 1994Jun 13, 1995Ciba-Geigy CorporationMoth- and beetle-proofing formulation
US5429918 *Aug 19, 1993Jul 4, 1995Fuji Photo Film Co., Ltd.Silver halide color photographic material
US5432468 *Oct 20, 1994Jul 11, 1995Nec CorporationClock generator circuit for use in a personal computer system
US5500424 *Aug 12, 1994Mar 19, 1996Nihon Nohyaku Co., Ltd.Pyrimidine and pyridine derivatives, their production and use
US5508288 *Mar 4, 1993Apr 16, 1996Smithkline Beecham, P.L.C.Indole derivatives as 5HT1C antagonists
US5596001 *Oct 25, 1993Jan 21, 1997Pfizer Inc.4-aryl-3-(heteroarylureido)quinoline derivatves
US5597719 *Jul 14, 1994Jan 28, 1997Onyx Pharmaceuticals, Inc.Interaction of RAF-1 and 14-3-3 proteins
US5624937 *Mar 2, 1995Apr 29, 1997Eli Lilly And CompanyChemical compounds as inhibitors of amyloid beta protein production
US5658903 *Jun 3, 1996Aug 19, 1997Smithkline Beecham CorporationImidazole compounds, compositions and use
US5710094 *Oct 27, 1995Jan 20, 1998Nippon Paper Industries Co. Ltd.Reversible multi-color thermal recording medium
US5773459 *Jun 7, 1995Jun 30, 1998Sugen, Inc.Urea- and thiourea-type compounds
US5780483 *Aug 21, 1996Jul 14, 1998Smithkline Beecham CorporationIL-8 receptor antagonists
US5886044 *Mar 20, 1996Mar 23, 1999Smithkline Beecham CorporationIL-8 receptor antagonists
US5891895 *Apr 14, 1997Apr 6, 1999Takeda Chemical Industries, Ltd.Hydroxypyridine derivatives their production and use
US5908865 *May 13, 1997Jun 1, 1999Senju Pharmaceutical Co., Ltd.Chlorhexidine gluconate-containing, stabilized aqueous pharmaceutical preparations
US5929250 *Jul 23, 1998Jul 27, 1999Smithkline Beecham CorporationIL-8 receptor antagonists
US6015908 *Apr 16, 1999Jan 18, 2000Smithkline Beecham CorporationIL-8 receptor antagonists
US6020345 *Nov 20, 1997Feb 1, 2000Pierre Fabre MedicamentPyridin-2-yl-methylamine derivatives, method of preparing and application as medicine
US6022884 *Nov 3, 1998Feb 8, 2000Amgen Inc.Substituted pyridine compounds and methods of use
US6040339 *May 28, 1998Mar 21, 2000Sankyo Company, LimitedUrea derivatives having ACAT inhibitory activity, their preparation and their therapeutic and prophylactic use
US6043374 *Oct 13, 1999Mar 28, 2000Smithkline Beecham CorporationBenzisothiazolidine Compounds
US6080763 *Oct 29, 1998Jun 27, 2000Boehringer Ingelheim Pharmaceuticals, Inc.Aromatic heterocyclic compounds and their use as anti-inflammatory agents
US6093742 *Jun 27, 1997Jul 25, 2000Vertex Pharmaceuticals, Inc.Inhibitors of p38
US6174901 *Dec 18, 1998Jan 16, 2001Amgen Inc.Substituted pyridine and pyridazine compounds and methods of use
US6178399 *Apr 24, 1995Jan 23, 2001Kabushiki Kaisha ToshibaTime series signal recognition with signal variation proof learning
US6180675 *Jan 29, 1999Jan 30, 2001Smithkline Beecham CorporationIL-8 receptor antagonists
US6187799 *May 22, 1998Feb 13, 2001Onyx PharmaceuticalsInhibition of raf kinase activity using aryl ureas
US6211373 *Jul 8, 1998Apr 3, 2001Smithkline Beecham CorporationPhenyl urea antagonists of the IL-8 receptor
US6218539 *Jun 24, 1997Apr 17, 2001Smithkline Beecham CorporationIL-8 receptor antagonists
US6242601 *Jan 13, 2000Jun 5, 2001Hoffman-La Roche Inc.Heterocyclic sulfamides
US6262113 *Aug 21, 1996Jul 17, 2001Smithkline Beecham CorporationIL-8 receptor antagonists
US6271261 *Jun 24, 1997Aug 7, 2001Smithkline Beecham CorporationIL-8 receptor antagonists
US6339045 *Dec 26, 1996Jan 15, 2002Kureha Kagaku Kogyo Kabushiki KaishaN-(unsubstituted or substituted)-4-substituted-6-(unsubstituted or substituted)phenoxy-2-pyridinecarboxamides or thiocarboxamides, processes for producing the same, and herbicides
US6344476 *May 22, 1998Feb 5, 2002Bayer CorporationInhibition of p38 kinase activity by aryl ureas
US6358945 *Feb 16, 2000Mar 19, 2002Boehringer Ingelheim Pharmaceuticals, Inc.Compounds useful as anti-inflammatory agents
US6372773 *Aug 2, 2001Apr 16, 2002Boehringer Ingelheim Pharmaceuticals, Inc.Aromatic heterocyclic compounds as antiinflammatory agents
US6380218 *Mar 10, 1998Apr 30, 2002Pfizer IncNicotinamide derivatives
US6391917 *Apr 19, 2001May 21, 2002Zymogenetics, Inc.Dialkyl ureas as calcitonin mimetics
US6414011 *Mar 24, 2000Jul 2, 2002Euro-Celtique S.A.Aryl substituted pyrazoles, and pyrroles, and the use thereof
US6525046 *Jun 7, 2002Feb 25, 2003Boehringer Ingelheim Pharmaceuticals, Inc.Aromatic heterocyclic compounds as antiinflammatory agents
US6525091 *Feb 22, 2002Feb 25, 2003Telik, Inc.Substituted diarylureas as stimulators for Fas-mediated apoptosis
US6583282 *Jul 6, 2000Jun 24, 2003Boehringer Ingelheim Pharmaceuticals, Inc.Process for synthesis of heteroaryl-substituted urea compounds useful as antiinflammatory agents
US6608052 *Apr 13, 2001Aug 19, 2003Boehringer Ingelheim Pharmaceuticals, Inc.Compounds useful as anti-inflammatory agents
US7235576 *Jan 11, 2002Jun 26, 2007Bayer Pharmaceuticals CorporationOmega-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
US7253286 *Apr 18, 2003Aug 7, 2007Eisai Co., LtdNitrogen-containing aromatic derivatives
US7547695 *Oct 14, 2004Jun 16, 2009Merck Patent GmbhPyridopyrimidinones
US20020065283 *Sep 7, 2001May 30, 2002Mcmahon GeraldHeteroarylcarboxamide compounds active against protein tyrosine kinase related disorders
US20020065296 *Apr 20, 2001May 30, 2002Bayer CorporationHeteroaryl ureas containing nitrogen hetero-atoms as p38 kinase inhibitors
Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US7838541Feb 11, 2003Nov 23, 2010Bayer Healthcare, LlcAryl ureas with angiogenesis inhibiting activity
US7897623Aug 27, 2007Mar 1, 2011Bayer Healthcare Llcω-carboxyl aryl substituted diphenyl ureas as p38 kinase inhibitors
US8076488Mar 1, 2004Dec 13, 2011Bayer Healthcare LlcBicyclic urea derivatives useful in the treatment of cancer and other disorders
US8124630Nov 27, 2001Feb 28, 2012Bayer Healthcare Llcω-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
US8242147Sep 23, 2010Aug 14, 2012Bayer Healthcare LlcAryl ureas with angiogenisis inhibiting activity
US8618141Jul 18, 2012Dec 31, 2013Bayer Healthcare LlcAryl ureas with angiogenesis inhibiting activity
US8637553Jul 22, 2004Jan 28, 2014Bayer Healthcare LlcFluoro substituted omega-carboxyaryl diphenyl urea for the treatment and prevention of diseases and conditions
US8680124Jan 18, 2008Mar 25, 2014Bayer Healthcare LlcTreatment of cancers with acquired resistance to kit inhibitors
US8796250May 19, 2004Aug 5, 2014Bayer Healthcare LlcDiaryl ureas for diseases mediated by PDGFR
US8841330Feb 8, 2012Sep 23, 2014Bayer Healthcare LlcOmega-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
US8883438Sep 14, 2012Nov 11, 2014Agios Pharmaceuticals, Inc.Method for diagnosing cell proliferation disorders having a neoactive mutation at residue 97 of isocitrate dehydrogenase 1
US9434979Apr 20, 2012Sep 6, 2016Shin-San Michael SuMethods and compositions for cell-proliferation-related disorders
US9458107Apr 15, 2014Oct 4, 2016Bayer Intellectual Property GmbhProcess for the preparation of 4-{4-[({[4 chloro-3-(trifluoromethyl)-phenyl]amino}carbonyl)amino]-3-fluorphenoxy-N-ethylpyridie-carboxamide, its salts and monohydrate
US9458781 *May 5, 2014Oct 4, 2016Toyota Jidosha Kabushiki KaishaControl device of internal combustion engine and method of controlling the same
US9474779Jan 18, 2013Oct 25, 2016Agios Pharmaceuticals, Inc.Therapeutically active compositions and their methods of use
US9512107Jun 3, 2016Dec 6, 2016Agios Pharmaceuticals, Inc.Therapeutically active compositions and their methods of use
US20050038080 *Jul 22, 2004Feb 17, 2005Stephen BoyerFluoro substituted omega-carboxyaryl diphenyl urea for the treatment and prevention of diseases and conditions
US20070020704 *May 19, 2004Jan 25, 2007Scott WilhelmDiaryl ureas with kinase inhibiting activity
US20080105264 *Dec 31, 2007May 8, 2008Resmed LimitedNasal assembly
US20080242707 *Feb 22, 2006Oct 2, 2008Bayer Healthcare AgPharmaceutical Composition for the Treatment of Cancer
US20100173953 *Sep 29, 2007Jul 8, 2010Alfons Grunenberg4-[4-(amino)-3-fluorophenoxy]-N-methylpyridine-2-carboxamide monohydrate
US20140331649 *May 5, 2014Nov 13, 2014Toyota Jidosha Kabushiki KaishaControl device of internal combustion engine and method of controlling the same
WO2014062511A1 *Oct 11, 2013Apr 24, 2014Agios Pharmaceuticals, Inc.Therapeutic compounds and compositions
Classifications
U.S. Classification514/357, 546/332, 514/425, 548/545
International ClassificationC07D207/36, C07D213/04, A61P19/02, A61K31/44, A61K31/5375, A61K31/4035, A61K31/341, A61K31/381, A61K31/40, A61K31/17
Cooperative ClassificationA61K31/4035, A61K31/341, A61K31/381, A61K31/5375, A61K31/44, A61K31/17
European ClassificationA61K31/44, A61K31/4035, A61K31/5375, A61K31/381, A61K31/17, A61K31/341
Legal Events
DateCodeEventDescription
Jul 27, 2009ASAssignment
Owner name: BAYER HEALTHCARE LLC, NEW YORK
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:BAYER PHARMACEUTICALS CORPORATION;REEL/FRAME:023031/0963
Effective date: 20071219
Owner name: BAYER HEALTHCARE LLC,NEW YORK
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:BAYER PHARMACEUTICALS CORPORATION;REEL/FRAME:023031/0963
Effective date: 20071219