CA2475703A1 - Aryl ureas with angiogenesis inhibiting activity - Google Patents

Aryl ureas with angiogenesis inhibiting activity Download PDF

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Publication number
CA2475703A1
CA2475703A1 CA002475703A CA2475703A CA2475703A1 CA 2475703 A1 CA2475703 A1 CA 2475703A1 CA 002475703 A CA002475703 A CA 002475703A CA 2475703 A CA2475703 A CA 2475703A CA 2475703 A1 CA2475703 A1 CA 2475703A1
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CA
Canada
Prior art keywords
group
phenyl
pyridinyl
alkyl
independently selected
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CA002475703A
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French (fr)
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CA2475703C (en
Inventor
Jacques Dumas
William J. Scott
James Elting
Holia Hatoum-Makdad
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Bayer Healthcare LLC
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Individual
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    • A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/5375—1,4-Oxazines, e.g. morpholine
    • A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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Abstract

This invention relates to methods of using aryl ureas to treat diseases mediated by the VEGF induced signal transduction pathway characterized by abnormal angiogenesis or hyperpermeability processes.

Description

Invest. 1995, 73, 859) 'and several intracranial tumors (Plate et al. Nature 1992, 359, 845; Phillips et al. Int. J. Oncol. 1993, 2, 913; Berkman et al. J. Clin.
Invest., 1993, 91, 153). Neutralizing monoclonal antibodies to KDR have been shown to be efficacious in blocking tumor angiogenesis (Kim et al. Nature 1993, 36~, 841;
Rockwell et al. Mol. Cell. Differ. 1995, 3, 315).
Qver expression of VEGF, for example under conditions of extreme hypoxia, can lead to intraocular angiogenesis, resulting in hyperproliferation of blood vessels, leading eventually to blindness. Such a cascade of events has been observed for a number of retinopathies, including diabetic retinopathy, ischemic retinal-vein occlusion, retinopathy of prematurity (Aiello et al. Nevv L'ngl. J. Med. 1994, 331, 1480; Peer et al. Lab. Invest. 1995, 72, 638), and age-related macular degeneration (AMD; see, Lopez et al. Invest. Opththalmol. Yis. Sci. 1996, 37, 855).
In rheumatoid arthritis (RA), the in-growth of vascular pannus may be mediated by production of angiogenic factors. Levels of immunoreactive VEGF
are high in the synovial fluid of RA patients, while VEGF levels were low in the synovial fluid of patients with other forms of arthritis of with degenerative joint disease (Koch et al. J. Immuraol. 1994, 152, 4149). The angiogenesis inhibitor AGM-170 has been shown to prevent neovascularization of the joint in the rat collagen arthritis model (Peacock et al. J. Exper. Med. 1992, 175, 1135).
Increased VEGF expression has also been shown in psoriatic skin, as well as bullous disorders associated with subepidermal blister formation, such as bullous . pemphigoid, erythema multiforme, and dermatitis herpetiformis (Brown et al.
J.
Invest. Dermatol. 1995,104, 744).
Because inhibition of KDR leads to inhibition of VEGF-mediated angiogenesis and permeabilization, KDR inhibitors will be useful in treatment of diseases characterized by abnormal angiogenesis and/or hyperpermeability processes, including the above listed diseases Summary of the Invention The present invention provides a method for treating diseases in humans or other mammals which are mediated by the VEGF induced signal transduction pathway, including those characterized by abnormal angiogenesis or hyperpermiability processes. These methods comprise administering a compound of formula I below or a salt, prodrug or stereoisomer thereof to a human or other mammal with a disease characterized by abnormal angiogenesis or hyperpermiability processes.
The compounds of formula I, which include all stereoisomeric forms (both ~ isolated and in mixtures) salts thereof and prodrugs thereof are collectively referred to herein as.the "compounds of the invention."
Formula I is as follows:
A_NH_C(O)_NH_B . I
wherein A is selected from the group consisting of (i) phenyl, optionally substituted with 1-3 substituents independently selected from the group consisting of Rl, ORI, NRIRz, S(O)qRl, SO2NRIRz, NRISOzRz, C(O)R', C(O)OR', C(O)NRIRz, NR1C(O)Rz, NR'C(O)ORz, halogen, cyano, and vitro;
(ii) naphthyl, optionally substituted with 1-3 substituents independently selected from the group consisting of Rl, ORI, NRIRz, S(O)qRl, SOzNRIRz, NR1SO2Rz, C(O)Ri, C(O)ORI, C(O)NRIRz, NR1C(O)Rz, NR1C(O)ORz, halogen, cyano, and vitro;
(iii) 5 and 6 membered monocyclic heteroaryl groups, having 1-3 heteroatoms independently selected from the group consisting of. O, N and S, optionally substituted with 1-3 substituents independently selected from the group consisting of Rl, ORI, NRIRz, .S(O)gRl, SOzNRIRz, NR1SOZRz, C(O)Rl, C(O)ORI, C(O)NRIRz, NR1C(O)Rz, NR1C(O)ORz, halogen, cyano, and vitro; and (iv) 8 to 10 membered bicyclic heteroaryl group in which the first ring is bonded to the NH of Figure I and contains 1-3 heteroatoms independently selected from the group .consisting of O, N, and S, and the second ring is fused to the first ring using 3 to 4 carbon atoms. The bicyclic heteroaryl group is optionally substituted with 5 1-3 substituents independently selected from the group consisting of Rl, ORI, NRIRa, S(O)qRl, SOZNR1R2, NR1SO2R2, C(O)Rl, . C(O)ORI, C(O)NR1RZ, NRiC(O)R2, NR1C(O)OR2, halogen, cyano, and vitro.
B is selected from the group consisting of (i) phenyl, optionally substituted with 1-3 substituents independently selected from the group consisting of -L-M, C1-Cs linear or branched alkyl, C1-Cs linear or branched haloalkyl, C1-C3 alkoxy, hydroxy; amino, C1-C3 alkylamino, C1-C6 dialkylamino, halogen, cyano, and vitro;
(ii) naphthyl, optionally substituted with 1-3 substituents independently selected from the group consisting of -L-M, CI-CS linear or branched alkyl, C1-Cs linear or branched haloalkyl, Cl-C3 alkoxy, hydroxy, amino, C1-C3 alkylamino, dialkylamino, halogen, cyano, and vitro;
(iii) 5 and 6 membered monocyclic heteroaryl groups, having 1-3 heteroatoms independently selected from the group consisting of O, N and S, optionally substituted with 1-3 substituents independently selected from the group consisting of -L-M, C1-Cs linear or branched alkyl, C1-Cs linear or branched haloalkyl, C1-C3 alkoxy, hydroxy, amino, C1-C3 alkylamino, C1-C6 dialkylamino, halogen, cyano, and vitro;
and' (iv)~ 8 to 10 membered bicyclic heteroaryl groups having 1-6 heteroatoms independently selected from the group consisting of O, N and S, optionally substituted with 1-3 substituents independently selected from the group consisting of -L-M, C1-Cs lineax.~or branched alkyl, C1-C5 linear or branched haloalkyl, C1-C3 alkoxy, hydroxy, amino, C1-C3 alkylamino, C1-C6 dialkylamino, halogen, cyano, and vitro.

L is selected from the group consisting of {a) -(CHz)m-O-(CHzO~
(b) -(CH2)n,-(CH2)~-(c) -(CHz)m C(O)-(CHz)~-, (d) -(CHz)n,-NR3-{CH2)1-, (e) -(CHz)m ~3C(O)-(CHz)r~
(~ -(CH2)ni S.-(CHz)in (g) -(CHz)m'C(O)~3 -{CH2)1-(h) -(CHz)m-CFz-{CHz)~-, (i) -(CHz)m CClz-(CHz)1-, U) -(CHz)m CHF-(CHz)r, (k) -(CHz)n.,-CH(OH)-(CHz),-;
(1) -{CHz)m C ~-(CHz)t-~ , (m) -(CHz)m-C=C-(CH2)1-a ~d I S (n) a single bond, where m and I are 0.; , (o) -(CHz)m CR4R5-(CHz)~-;
The variables m and l are integers independently selected from 0-4.
M is selected from the group consisting of (i) phenyl, optionally substituted with 1-3 substituents independently selected from the group consisting of Rl, OR1, NRIRz, S(O)qRl, SOZNR~R2, NR1S02R'', C{O)Rl, C(O)ORI, C{O)NRIRz, NR1C(O)Rz, NRrC(O)ORz, halogen, cyano and vitro;
(ii) naphthyl, optionally substituted with 1-3 substituents independently selected from the group consisting of Rl, ORI, NR,IRz, S(O)gRI, SOzNRiR2, ' NRISOzRz, C(O)Rl, C(O)ORS, C(O)NRIRz, NR1C(O)Rz, NR1C(O)ORz, halogen, cyano and vitro;
(iii), 5 and 6 membered monocyclic heteroaryl groups, having 1-3 heteroatorizs independently selected from the group consisting of O, N and S, optionally substituted with 1-3 substituents independently selected from the group consisting of Rl, ORI, NRIRz, S(O)qRl, SOzNRIRz, NRiSOZRz, C(O)Rl, C(O)ORI, C(O)NRIRz, NR1C(O)Rz, NR1C~0)ORz, halogen, cyano and vitro and also oxides (e.g. =O, -O-or -OH); and (iv) . 8 to 10 membered bicyclic heteroaryl groups, having 1-6 heteroatoms independently selected from the group consisting of O, N and S, optionally substituted with 1-3 substituents independently selected from the group consisting of Rl, ORS, NRIRz, S(O)qRl, SOzNRIRz, ~ NRISOzRz, C(O)Rl, C(O)ORI, C(O)NRlRz, NR1C(O)Rz, NR1C(O)ORz, halogen, cyano and vitro and also oxides (e.g. =O, -O-or -OH).
(v) saturated and partially saturated C3-C6 monocyclic carbocyclic moiety optionally substituted with 1-3 substituents independently selected from the group consisting of R', ORI, NRIRz, S(O)qRl, SOzNRIRz, NRISOZRz, C(O)Rl, C(O)ORI, C(O)NRIRz, NR1C(O)Rz, NR1C(O)ORz, halogen, cyano and, vitro;
(vi) saturated and partially saturated C$-Clo bicyclic carbocyclic moiety, optionally substituted with 1-3 substituents independently selected from the group consisting of Rl, ORI, NRIRz, S(O)qRl, SOzNRIRz, NR~SOZRz, C(O)Rl, C(O)ORt, C(O)NRtRz, NR1C(O)Rz, NR1C(O)ORz, halogen, cyano and vitro;
(vii) saturated and partially saturated 5 and 6 membered monocyclic heterocyclic moiety, having 1-3. heteroatoms independently selected from the group consisting of O, N and S, optionally substituted with 1-3 substituents independently selected from the group consisting of Rl, ORI, NRIRz, S(O)qRl, SOzNRIRz, NR1SOZRz, C(O)Ri, C(O)ORI, C(O)NRIRz, NR1C(O)Rz, NR1C(O)ORz, halogen, cyano and vitro, and also oxides (e.g. =O, -O~ or -OH); and (viii) saturated and partially saturated 8 to 10 membered bicyclic heterocyclic moiety, having 1-6 heteroatoms independently selected from the group consisting of O, N and S, optionally substituted with I-3 substituents independently selected from the group consisting of Rl, OR1, NR1R2, S(O)qRl, SOzNRIRz, NR1SOZRz, C(O)Rl, C(O)ORI, C(O)NRIRz, NRIC(O)Rz, NR1C(O)ORz, halogen; cyano and vitro, and also oxides (e.g. =O, -O- or-OH).
Each Rn- RS are independently selected from the group consisting of:
(a) hydrogen, (b) C1-C6 alkyl, preferably, Cl-C5 linear, branched, or cyclic alkyl, wherein said alkyl is optionally substituted with halogen up to per-halo; .
(c) phenyl;
(d) 5-6 membered monocyclic heteroaryl having 1-4 heteroatoms selected from the S group consisting of O, N and S or 8-10 membered bicyclic heteroaryl having 1-heteroatoms selected from the group consisting of O, N and S;
(e)_ CI-C3 alkyl-phenyl wherein said alkyl moiety ~ is optionally substituted with halogen up to per-halo; and (fj C1-C3 alkyl-heteroaryl having 1-4 heteroatoms selected from the group consisting of O, N and S, wherein said heteroaryl group is a 5-6 membered monocyclic heteroaryl or a 8-10 membered bicyclic heteroaryl, and wherein said,alkyl moiety is optionally substituted with halogen up td per-halo.
Each Rl - R5, when not hydrogen is optionally substituted with 1-3 substituents independently selected from the group consisting of C1-CS linear branched or cyclic alkyl, wherein said alkyl is optionally substituted with halogen up to per-halo, C1-C3 alkoxy, wherein said alkoxy is optionally substituted with halogen up to per-halo, hydroxy, amino, C1-C3 alkylamino, Ca-C6 dialkylamino, halogen, cyano, and nitro;
Each variable q is independently selected from 0, 1, or 2.
Suitable substituted and unsubstituted heteroaryl groups for the compounds of this invention, such as those for A, B and M of formula I, include, but are not limited to the following monocyclic heteroaryl groups:
2- and 3-furyl, 2- and 3-thienyl, 2- and 4'-triazinyl, 1-, ?- and 3-pyrrolyl, 1-,.2-, 4- and 5-imidazolyl, 1-, 3-, 4- and 5-pyrazolyl, 2-, 4- and 5-oxazolyl, 3-, 4-and 5-isoxazolyl, 2-, 4- and 5-thiazolyl, 3-, 4- and 5-isothiazolyl, 2-, 3- and 4-pyridyl, 2-, 4-, 5- and 6-pyrimidinyl, 1,2,3-triazol-1-, -4-_and -5-yl, 1;2,4-triazol-1-; -3-and -5-yl, 1-and 5-tetrazolyl, 1,2,3-oxadiazol-4- and -5-yl, 1,2,4-oxadiazol-3- and -5-yl, 1,3,4-thiadiazol-2- and -5-yl, 1,2,4-oxadiazol-3- and -5-yl, 1,3,4-thiadiazol-2- and -5-yl, 1,3,4-thiadiazol-3- and -5-yl, 1,2,3-thiadiazol-4- and -5-yl, 2-, 3-, 4-, 5-and 6-2H-thiopyranyl, 2-, 3- and 4-4H-thiopyranyl, 3- and 4-pyridazinyl, 2-,3-pyrazinyl, and bicyclic heteroaryl groups such as Benzofuryl, benzothienyl, indolyl, benzimidazolyl, benzopyrazolyl, benzoxazolyl, benzisoxa.zolyl, benzothiazolyl, benzisothiazolyl, benz-1,3-oxadia.zolyl, quinolinyl, isoquinolinyl, quinazolinyl, tetrahydroquinolinyl, tetrallydroisoquinolinyl, dihydrobenzofuryl, pyrazolo[3,4-b]pyrimidinyl, purinyl, benzodiazine, pterindinyl, pyrrolo[2,3-b]pyridinyl, pyrazolo[3,4-b]pyridinyl, oxazo[4,5-b]pyridinyl, imidazo[4,5-b]pyridinyl, cyclopentenopyridine, cyclohexanopyridine, cyclopentanopyrimidine, cyclohexanopyrimidine, cyclcopentanopyrazine, cyclohexanopyrazine, cyclopentanopyridiazine, cyclohexanopyrida.zine, .cyclopentanoimidazole, cyclohexanoimidazole, cyclopentanothiopherie and cyclohexanothiophene.
Suitable aryl groups which do not contain heteroatoms include, for example, phenyl and 1- and 2-naphthyl, tetrahydronaphthyl, indanyl, indenyl, benzocyclobutanyl, benzocycloheptanyl and benzocycloheptenyl.
Suitable linear alkyl groups and alkyl portions of groups, e.g., alkoxy, alkylphenyl and alkylheteroaryl etc. throughout include methyl, ethyl, propyl, butyl, pentyl; etc. . Suitable branched alkyl groups- include all branched isomers such as isopropyl, isobutyl, sec-butyl, test-butyl, etc.
Suitable halogen groups include F, ~ Cl, Br, and/or I, from one to ~ per-substitution (i.e.. all H atoms oma 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. Preferred halogens are Cl, Br and F.
The term "up to perhalo substituted linear and branched alkyl," includes alkyl groups having one alkyl hydrogen replaced with halogen, alkyl groups wherein all hydrogens are replaced with halogen, alkyl groups wherein more than one but less than all hydrogens are replaced by halogen and alkyl groups having alkyl hydrogens replaced by halogen and other substituents.

The term "cycloalkyl", as used herein, refers to cyclic structures having 3-8 members in the ring such as cyclopropyl, cyclobutyl and cyclopentyl and cyclic structures having 3-8 members with alkyl substituents such that, for example, "C3 5 cycloalkyl" includes methyl substituted cyclopropyl groups.
The term "saturated carbocyclic moieties" defines only the cyclic structure, i.e.
cyclopentyl, cyclohexyl, etc. Any alkyl substitution on these cyclic structures is specifically identif ed.
Saturated monocyclic and bicyclic. carbocyclic moieties include cyclopropyl, cyclobutyl,~cyclopentyl, cyclohexyl, and decahydronapthalene.
Partially saturated monocyclic and bicyclic carbocyclic moieties include I S cyclopentenyl, cyclohexenyl, cyclohexadienyl and tetrahydronaphthalene.
Saturated monocyclic and bicyclic heterocyclic moieties include tetrahydropyranyl, tetrahydrofuranyl, 1,3-dioxolane, 1,4-dioxanyl, morpholinyl, thiomorpholinyl, piperazinyl, , piperidinyl, piperidinonyl, tetrahydropyrimidonyl, pentamethylene sulfide and tetramethylene sulfide.
Partially saturated monocyclic and bicyclic heterocyclic moieties include dihydropyranyl, dihydrofuranyl, dihydrothienyl, dihydropiperidinyl, and dihydropyrimidonyl.
A subclass of compounds of this invention is defined by formula I, wherein A
B and M are selected from phenyl, naphthyh. furyl, isoindolinyl, oxadiazolyl, oxazolyl, isooxazolyl, pyrazolyl, pyridinyl, pyrimidinyl, pyrrolyl, quinolinyl, isoquinolinyl, tetrazolyl, thiadiazolyl, thiazolyl and thienyl and are optionally substituted as defined ~ above:

Preferred substituents for B include methyl, trifluoromethyl, ethyl, n-propyl, n butyl, n-pentyl, isopropyl, isobutyl, sec-butyl, tent-butyl, cyclopropyl, cyclobutyl, cyclopentyl, methoxy, ethoxy, propoxy, Cl, Br and F, cyano, vitro, hydroxy, amino, methylamino, dimethylamino, ethylamino and diethylamino as well as the structure -L-M.
Preferred substituents for A and M include methyl, trifluoromethyl, ethyl, n-propyl, n-butyl, n-pentyl, isopropyl, text-butyl, sec-butyl, isobutyl, cyclopropyl, cyclobutyl, cyclopentyl, , methoxy, ethoxy, propoxy, Cl, Br, and F,. cyano, vitro, hydroxy, amino, methylamino, dimethylamino, ethylamino and diethylamino and fiuther include:
phenyl, pyridinyl, pyrimidinyl, chlorophenyl, dichlorophenyl, bromophenyl, dibromophenyl, chloropyridinyl, bromopyridinyl, dichloropyridinyl, dibromopyridinyl methylphenyl, methylpyridinyl quinolinyl, isoquinolinyl, isoindolinyl, pyrazinyl, pyridazinyl, pyrrolinyl, imidazolinyl, thienyl, furyl, isoxazolinyl, isothiazolinyl, benzopyridinyl, benzothiazolyl, C1-CS acyl; _ NH(C1-CS alkyl, phenyl or pyridinyl), such as aminophenyl;
N(C1-CS alkyl)(C1-CS alkyl, phenyl or pyridinyl), such as diethylamino and dimethyl amino;
S(O)9 (C1-CS alkyl); such as methanesulfonyl;
S(O)a H;
SO2NH2;
SOzNH(C1-CS alkyl);
SO2N(C1-CS alkyl)(C1-CS alkyl); .
NHSOz(Ci-CS alkyl); N(C1-C3 alkyl) SOz(C1-CS alkyl);
CO(Ci-C6 allcyl or phenyl); , C(O)H; .
C(O)O(C1-C6 alkyl or phenyl), such as C(O)OCH3, -C(O)OCH2CH3, ~-C(O)OCHaCHaCH3;
C(O)OH; . : .
C(O)NH2 (carbamoyl);

C(O)NH(C1-C6 alkyl or phenyl), such as N-methylethyl carbamoyl, N-methyl carbamoyl, N-ethylcarbamoyl, or N-dimethylamino ethyl carbamoyl;
C(O)N(C1-C6 alkyl or phenyl)(Cl-C6 alkyl, phenyl or pyridinyl), such ~as N-dimethyl carbamoyl;
C(N(C1-Cs alkyl)) (C1-CS alkyl);
NHC(O)(C1-C6 alkyl or phenyl) and N(C1-CS alkyl,)C(O)(C1-Cs alkyl).
Each of the above substituents is optionally partially or fully halogenated, such as difluoromethyl sulfonyl.
An embodiment of this invention includes the administration of compounds of this invention wherein in formula I, A, B and M follow one of the following of combinations:
A= phenyl, B=phenyl and M is phenyl, pyridinyl, quinolinyl, isoquinolinyl or not present, A= phenyl, B=pyridiriyl and M is phenyl, pyridinyl, quinolinyl, isoquinolinyl or not present, A=phenyl, B = naphthyl and M is phenyl, pyridinyl, quinolinyl, isoquinolinyl or not present, A~yridinyl, B= phenyl and M is phenyl, pyridinyl, quinolinyl, isoquinolinyl or not present, A=pyridinyl, B= pyridinyl and M is phenyl, pyridinyl, quinolinyl, isoquinolinyl or not present, ~ , A=pyridinyl, B= naphthyl and M is.phenyl, pyridinyl, quinolinyl, isoquinolinyl or not piesent, A=isoquinolinyl, B= phenyl and M is phenyl, pyridinyl, quinolinyl, isoquinolinyl or not present, A= isoquinolinyl, B= pyridinyl and M is phenyl, pyridinyl, quinolinyl, isoquinolinyl or not present, -~ A= isoquinolinyl, B= naphthyl , and M is phenyl, pyridinyl, quinolinyl, isoquinolinyl or not present, A= quinolinyl, B= phenyl and M is phenyl, pyridinyl, quinolinyl, isoquinolinyl or not present, A= quinolinyl, B= pyridinyl and M is phenyl, pyridinyl, quinolinyl, _ isoquinolinyl or not present, A= quinolinyl, B,= naphthyl and M is phenyl, pyridinyl, quinolinyl, isoquinolinyl or not present.
The structure L of formula I is preferably. -O-, a single bond, -S-, -NH-, -N(CH3)-, -NHCHz-, - NCZHd-, -CHz-, -C(O)-, -CH(OH)-, -NHC(O)N(CH3)CHz-, _ N(CH3)C(O)N(CH3)CHz-, ~ -CH2C(O)N(CH3)-, -C(O)N(CH3)CHz-, -NHC(O)-, -N(CH3)C(O)-, -C(O)N(CH3)-, -C(O)NH-, -CH20-, -CHzS-, -CHzN(CH3)-, -OCHZ-, -CHF-, -CFz-,-CCIz-, -S-CHz- , and N(CH3)CHz- .
One of ordinary skill in the art will recognize that some of the compounds of Formula (I) can exist in different geometrical isorrieric forrris. A number of the compounds of Formula I possess asymmetric carbons and can therefore exist in racemic and optically active forms as well as in' the form of racemic or non-racemic mixtures thereof, and in the form of diastereomers and diastereomeric mixtures. All of these compounds, including cis isomers, traps isomers, diastereomic mixtures, racemates, non-racemic mixtures of enantioiners, substantially pure; and pure enantiomers, are considered to be within the scope of the present invention and are collectively referred to when reference is made to 'compounds of this invention.
Methods of separation of enantiomeric and diastereomeric mixtures are well known to one skilled in the art. The optical isomers can be obtained by resolution of the racemic mixtures according to conventional processes, for example, by the formation of diastereoisomeric salts using an optically active acid or base.
Examples of appropriate acids are tartaric, diacetyltartaric, dibenzoyltartaric, ditoluoyltartaric and camphorsulfonic acid. Mixtures of diastereoisomers can be separated into their individual diastereomers on the basis of their physical chemical differences by methods known to those skilled in the art, for example, by chromatography or fractional crystallization. The optically active bases or acids are liberated from the separated diastereomeric salts.
Another process. for separation of optical isomers involves the use of a chiral chromatography column (e.g., chiral HPLC columns) optimally chosen to maximize the separation of the enantiomers. Suitable chiral HPLC columns are manufactured by Diacel, e.g., Chiracel OD and Chiracel OJ. The optically active compounds of Formula (I) can likewise be obtained by utilizing optically active starting materials.
10. The present invention encompasses any isolated racemic or optically active form of compounds described in Formula I which possess angiogenesis 'inhibitory' activity. The term _ stereoisomer is understood to encompass diastereoisomers, enantiomers, geometric isomers, etc. Herein, , substantially pure enantiomers is intended to mean that no more than 5% w/w of the corresponding opposite enantiomer is present.
Pharmaceutically acceptable salts of these compounds as well as commonly used prodrugs of these compouilds are also within the scope of the invention.
Salts are especially the pharmaceutically acceptable salts of compounds of formula (l~ or such as, for example, organic or inorganic acid addition salts of compounds of formula (I). Suitable inorganic acids include but are not limited to halogen acids (such as hydrochloric acid and hydrobromic acid), sulfuric acid, or phosphoric acid. Suitable organic acids include but are not limited to carboxylic, phosphoric, sulfonic, or sulfamic acids, with examples including acetic acid, propionic acid, octanoic acid, decanoic acid, trifluoroacetic acid, dodecanoic acid, glycolic acid, lactic acid, 2- or 3-hydroxybutyric acid, y aminobutyric acid (GABA), gluconic .acid, glucosemonocarboxylic acid, benzoic acid, salicylic acid, pheny~acetic acid and mandelic acid, fumaric acid, succinic acid, adipic acid, pimelic acid,, suberic acid, azeiaic acid, malic acid, tartaric acid, citric acid, glucaric acid, galactaric acid, amino acids (such as glutamic acid, aspartic acid, N-methylglycine, acetytaminoacetic acid, N-acetylasparagine or N-acetylcysteine), pyruvic acid, acetoacetic acid, methanesulfonic acid, tri-fluoromethane sulfonic acid, 4-toluene sulfonic acid, benzenesulfonic acid, 1-naphthalenesulfonic acid, 2-naphthalenesulfonic acid, phosphoserine, and 2- or 3-glycerophosphoric acid.
5 Iri addition, pharmaceutically acceptable salts include acid salts of inorganic bases, such as salts containing alkaline ~ cations (e.g., Li+ Nay or K+), alkaline earth cations (e.g., Mg+Z, 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 10 triethylamine, N,N diethylamine, N,N dicyclohexylamine, lysine, pyridine, N,N
dimethylaminopyridine (DMAP), 1,4-diazabiclo[2.2.2]octane (DA.BCO), 1,5-diazabicyclo[4.3.0]non-5-ene (DBN) and 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU).
The formation of prodrugs is well known in the art in order to enhance the 15 properties of the parent compound; such properties include solubility, absorption, biostability and release time (see "Pharmaceutical Dosage Form and Drug Deliver Systems" ,(Sixth Edition), edited by Ansel et al., published by Williams &
Wilkins, pages 27-29,. (1995) which is hereby incorporated by ,reference). Commonly used prodrugs of the disclosed oxazolyl-phenyl-2,4-diamino-pyrimidine compounds are designed to take advantage of the major drug biotrarisformation reactions and are also to be considered within the scope of the invention. Major drug biotransformation reactions include N-dealkylation, O-dealkylation, aliphatic hydroxylation, aromatic hydroxylation, N-oxidation, S-oxidation, deamination, hydrolysis, reactions, glucuronidation, sulfation and acetylation . (see Goodman and (Jilman's 1 he Pharmacological Basis of Therapeutics (Ninth Edition), editor Molinoff et al., pub. by McGraw-Hill, pages 11-13, (1996), which is hereby incorporated by reference).
The invention also relates to methods for treating and preventing diseases, for example; angiogenesis disorders in mammals by ,administering a compound of this invention or a pharmaceutical composition comprising one or more compounds of this invention.

A compound according to the invention can be administered simultaneously with another angiogenesis inhibiting agent to a patient with such a disorder, in the same formulation or, more typically in separate formulations and, often, using different administration routes. Administration can also be sequentially, in any order.
A compound according to the invention can be administered in tandem with another angiogenesis inhibiting agent,, wherein a compound according to the invention can be administered to a patient once or more per day for up to 28 consecutive days with the concurrent or intermittent administration of another angiogenesis inhibiting a agent over the same total time period.
A compound according to the invention can be administered to a patient at an oral, intravenous, intramuscular, subcutaneous, or parenteral dosage which can range from about 0.1 to about 200 mg/kg ,of total body weight and the additional angiogenesis inhibiting agent can be administered to a patient at an intravenous, intramuscular, subcutaneous, or parenteral dosage which can range from about 0.1 mg to 200 mg/kg of patient body weight.
An embodiment of the present invention is a method for treating diseases in humans and/or other mammals which . are mediated by the VEGF induced signal transduction pathway which comprises administering a compound of this invention to a human or other mammal.
Another. embodiment of this invention is a method for treating diseases in humans and/or other mammals which are characterized by abnormal angiogenesis or hyperperlniability,processes with a compound of this invention to a human or other mammal.
Another embodiment of this. invention is a method for treating diseases in humans and/or other mammals which are characterized by abnormal angiogenesis or hyperpermiability processes, which are not raf mediated, which comprises , administering a compound of this invention to a human or.other mammal.

Another embodiment of this invention is a method for treating diseases in humans and/or other mammals which are characterized by abnormal angiogenesis or hyperpermiability processes, which are not - raf mediated or p38-mediated, which comprises administering a compound of this invention to a human or other mammal.
Another embodiment of this, invention is a method for treating diseases in humans and/or other mammals which are characterized by abnormal angiogenesis or hyperpermiability processes, which are raf mediated and/or p38 mediated, which comprises administering a compound of this invention to a human or other mammal.
Another embodiment of this invention is a method for treating one or more of the following conditions in humans and/or other mammals: tumor growth, retinopathy, including diabetic retinopathy, ischemic retinal-vein occlusion, retinopathy of prematurity and age related macular degeneration; rheumatoid arthritis, psoriasis, or bullous disorder associated with subepidermal blister formation, including bullous pemphigoid, erythema multiforme, or dermatitis herpetiformis, which comprises administering a compound of this invention to a human or other mammal with one or more of these conditions.
Another embodiment of this invention is a method for treating one or more of the following conditions in humans and/or other mammals: tumor - growth, ~ retinopathy, diabetic retinopathy, ischemic retinal-vein occlusion, retinopathy of prematurity, age related macular degeneration; rheumatoid arthritis, psoriasis, bullous disorder associated with subepidermal blister formation, bullous~ pemphigoid, erythema multiforme, and dermatitis herpetiformis in combination with another condition selected from the group consisting of ~ rheumatic fever, bone resorption, postmenopausal osteoporosis, sepsis, gram negative sepsis, septic shock, endotoxic shock, toxic shock syndrome, systemic inflammatory response syndrome, inflammatory bowel disease (Crohn's disease and ulcerative colitis), Jarisch-Herxheimer reaction, asthma, adult respiratory distress syndrome, acute pulmonary fibrotic disease, pulmonary sarcoidosis, allergic respiratory disease, silicosis, coal worker's pneumoconiosis, alveolar injury;
hepatic failure, liver disease during acute inflammation, severe alcoholic hepatitis, malaria (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 (demyelation and oligiodendrocyte loss in multiple sclerosis), advanced . cancer, lymphoid malignancy, paricreatitis, impaired wound healing in infection, inflammation and cancer, myelodysplastic syndromes, systemic lupus erythematosus, biliary cirrhosis, bowel necrosis, radiation injuryl toxicity following administration of monoclonal antibodies, host-versus-graft reaction (ischemia reperfusion injury and allograft rejections of kidney, liver, heart, and skin), lung allograft rejection (obliterative bronchitis) or complications due to total hip replacement. This method comprises administering a compound of this invention to a human or other mammal with one of the above combinations of conditions. . .
Another embodiment of this invention is a method for treating one or more of the following conditions in humans and/or other mammals: ~ .
tumor growth, retinopathy, diabetic retinopathy, ischemic retinal-vein occlusion, retinopathy of prematurity, age related macular degeneration;.
rheumatoid arthritis, psoriasis, bullous disorder associated with subepidermal blister formation, hullous pemphigoid, erythema multiforme, and dermatitis herpetiformis, in'combination with an infectious disease selected from the group consisting of 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). These methods comprise administering a compound of this invention to a human or other mammal with a combination of one of the above infectious diseases and one of the above diseases characterized by abnormal angiogenesis or hyperpermiability processes.

This invention further relates to kits comprising separate doses of the two mentioned chemotherapeutic agents in separate containers. The combinations of angiogenesis inhibiting agents can also be formed in vivo, e.g., in a patient's body.
These angiogenesis inhibiting agents can be administered in the conventional formulations and regimens in which they are known for use alone.
Conditions within a human or other mammal which can be treated by administering a compound of this invention are those characterized by abnormal angiogenesis or hyperpermiability processes. Conditions to be treated include tumor growth, retinopathy, including diabetic retinopathy, ischemic retinal-vein occlusion, retinopathy of prematurity and age related macular degeneration; rheumatoid arthritis, psoriasis, or a bullous disorder associated with subepidermal blister formation, including bullous pemphigoid, erythema multifonne, and dermatitis herpetiformis.
Methods of interest include the treatment of combinations of the conditions above (tumor growth, retinopathy,. diabetic retinopathy, ischemic retinal-vein occlusion, retinopathy of prematurity, age related macular degeneration;
rheumatoid arthritis, psoriasis, bullous disorder associated with subepidermal blister formation, bullous p~mplugoid, erythema multiforme, and dermatitis herpetiformis) and another condition selected from the group.consisting of: . , . rheumatic fever, bone resorption, postmenopausal osteoperosis, sepsis; gram negative sepsis, septic shock, endotoxic shock, toxic shock syndrome, systemic inflammatory response syndrome, inflammatory bowel disease (Crohn's disease and ulcerative colitis), Jarisch-Herxheimer reaction,. asthma, adult respiratory distress yndrome, acute pulmonary fibrotic disease, pulmonary sarcoidosis, allergic respiratory disease, silicosis, coal worker's pneumoconiosis, alveolar injury, hepatic failure, liver disease during acute inflammation, severe alcoholic hepatitis, malaria (Plasmodium falciparum malaria and cerebral malaria), non-insulin-dependent diabetes mellitus (NmDM), congestive heart failure, damage following heart disease, atherosclerosis, Alzheimer's disease, acute encephalitis, ' brain injury, multiple sclerosis (demyelation and oligiodendrocyte loss in - multiple sclerosis), advanced cancer, lymphoid malignancy, pancreatitis, impaired wound healing in infection, inflammation and cancer, myelodysplastic syndromes, systemic lupus erythematosus, biliary cirrhosis, bowel necrosis, radiation injuryl toxicity following administration of monoclonal antibodies, host-versus-graft reaction (ischernia reperfusion injury and 5 allograft rejections ,of kidney, liver, heart, and skin), lung allograft rejection (obliterative bronchitis) or complications due to total hip replacement.
Also provided is a method for treating combinations of the conditions above (tumor growth, retinopathy, diabetic retinopathy, ischemic retinal-vein occlusion, 10 retinopathy of prematurity, age related . macular degeneration; rheumatoid arthritis, psoriasis, bullous disorder associated with subepidermal blister formation bullous pemphigoid, erythema multiforme, and dermatitis herpetiformis) and an infectious disease selected from the group consisting of 15 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 20 encephalomyelitis virus, and the human immunodeficiency virus (HIV).
The compounds of this invention can be made according to conventional chemical methods, and/or as disclosed below, from starting materials which are either commercially available or producible according to routine, conventional chemical methods. General methods ,for,the preparation of the compounds are given below, and the preparation of a suitable compound is specifically illustrated in the Examples.
Ureas of formula (I) can be prepared by a variety. of simple methods known in the art. General approaches for the formation of those compounds can be found in "Advanced Organic Chemistry ", by J. March, John Wiley and Sobs, 1985 and in "Comprehensive Organic Transformations ", by R. ~ C.' Larock, TlCH Publishers, 1989), which are hereby incorporated by reference. Nevertheless, the ,following general preparative methods are presented to aid one of skill in the art in synthesizing these compounds, with more detailed examples being presented in the experimental section describing the working examples.
General Preparative Methods Heterocyclic amines may be synthesized utilizing known methodology (I~atritzky, et al. Comprehensive FIeteYOCyclic -Chemistry; Permagon Press:
Oxford, UI~ (1984). March. Advaneed Organic Chemistry, 3ra Ed.; John Wiley: New York (1985)). For example, as shown in Scheme I, 5-arninopyrazoles substituted at the N 1 position with either aryl or heteroaryl moieties may be synthesized by the reaction of an oc-cyanoketone (2) with the appropriate aryl- or heteroaryl hydrazine (3, R2=aryl or heteroaryl). Cyanoketone 2, in turn, is available from the reaction of acetarnidate ion with , an appropriate acyl derivative, such as an ester, an acid halide, or an acid anhydride. In cases where the R2 moiety offers suitable anion stabilization, 2-aryl-and-2-heteroarylfurans may be synthesized from a Mitsunobu,reaction of cyanoketone 2 with alcohol 5, followed by base catalyzed cyclization of enol ether 6 to give furylamine 7.
CH3CN.
1 ) base ~ - R~

- ~

2) ~ N
~ ~ R NHNH2 y N
3
4 O

R~~CN - -.. 2 HO~CO2R2 5 .

R~ R~

- PPH3 ~ . _ base - _ EtO2CN=NCO2Et _ O\
- ) i~ _ CN
~

. , - NH2 ~ . 7 _ .

Scheme I. Selected General Methods for Heterocyclic Amine Synthesis Substituted anilines may be generated using standard methods (March.
Advanced Organic Chemistry, 3'~d Ed.; John Wiley: New Yorlc (1985). Larock.
C~mprehensive Organic Trarasforrnations; VCH Publishers: New York (1989)). As shown in Scheme II, aryl amines are commonly synthesized by reduction of nitroaryls using a metal catalyst, such as Ni, Pd, or Pt, and Hz or a hydride transfer agent, such as formate, cyclohexadiene, or a borohydride (Rylander. Hydrogenation Methods;
Academic Press: London, UK (1985)). Nitroaryls may also be directly reduced using a strong hydride source, such as LiAlH4 (Seyden-Penne. Reductions ~b~r the Alumino-and Borohyds-ides in Organic Sy~zthesis; VCH Publishers: New York (1991)), or using a zero valent metal, such as Fe, Sn or Ca, often in acidic media. Many methods exist for the synthesis of nitroaryls (March. Advanced Organic Chemistry, 3ra Ed.;
John Wiley: New York (1985).. Larock. Comprehensive Organic Transformations; VCH
Publishers: New York (1989)).
H~ / catalyst (eg. Ni, Pd; Pt) ArN02 ~H ~ ~ ArNH2 ~ M(o) (eg. Fe, Sn, Ca) Scheme II Reduction of Nitroaryls to Aryl Amines Nitroaryls are commonly formed by electrophilic aromatic nitration using .
HN03, or an alternative NOZ+ source. Nitro aryls may be further elaborated prior to .
reduction. Thus, nitroaryls substituted with Ar-H ~ ArNOZ
potential leaving groups (eg. F, Cl, .Br, etc.) may undergo substitution reactions on treatment with nucleophiles, such as thiolate (exemplified in Scheme III) or phenoxide. Nitroaryls may also undergo Ullman-type coupling reactions (Scheme IIt).

ArSH
base 8~ OzN
S-Ar Br-Ar g R j~SH .
Cu0 / base Scheme III Selected Nucleophilic Aromatic Substitution using Nitroaryls As shown in Scheme 1V, urea. formation may involve reaction of a heteroaryl
5 isocyanate (12) with an aryl amine (11). The heferoaryl isocyanate may be ynthesized from a heteroaryl amine by, treatment with phosgene or a phosgene equivalent, such ~s trichloromethyl chloroformate (diphosgene), bis(trichloromethyl) carbonate (triphosgene), or N,N'-carbonyldiimidazole (CDR. The isocyanate may also be derived from a heterocyclic carboxylic acid derivative, such as an ester, an acid 10 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 subj ected to Curtius-type rearrangements using diphenylphosphoryl azide (DPPA) or a similar reagent. A
urea . may also be generated from the reaction of an aryl isocyanate (15) with a heterocyclic , arriine.

Het-NH2 11 H2N-Ar 14 - H2N-Ar O Het-NH2 Het-NCO Het~N~N'Ar ~; OCN-Ar Ns DPPA N3 DPPA
Het X Het OH X Ar HO Ar 16 17 18 . 19 Scheme IV Selected Methods of Urea Formation (Het = heterocycle) Finally, areas may be further manipulated using methods familiar to those skilled in the art. Fox example, 2-aryl and 2-heteroarylthieriyl areas are available from the corresponding 2-halothienyl urea through transition metal mediated cross coupling .
reactions (exemplified with 2-bromothiophene 25, Scheme V). Thus, reaction, of nitrile 20 with an oc-thioacetate ester gives 5-substituted-3-amino-2-thiophenecarboxylate 21 (Ishizaki et al. JP 6025221). Decarboxylafion of ester may be achieved by protection of the amine, for example as the test-butoxy~(BOC) carbamate (22), followed by saponification and treatment with acid. When BOC
protection is used, decarboxylation may be accompanied by deprotection giving the substituted 3-thiopheneammonium salt 23. Alternatively, ammonium salt 23 may be directly generated through saponification of ester 21 followed by treatment with acid.
Following urea formation as described above, bromination affords penultimate halothiophene 25. Palladium mediated cross coupling of thiophene 25 with an appropriate tributyl- or trimethyltin (Ra= aryl or heteroaryl) then affords the desired 2-aryl- or 2-heteroarylthienyl urea.

R~
R~ ~ HS~C02R _ S ~
CI~ ~NH2 CN

~O~O~O~
R~ R~
_ 1 ) O H-S
S ~ NH3+ 2)_H+ . ~NHBOC

Ar-NCO
R~ R~ R~
0 Br2 ' O R2-SnMe3. ._ 0 S i N~N'Ar ~ S ~ N~N'Ar Pd(0) S /
~N~N'Ar H H Br. H H R2 H H

Scheme V Synthesis and Interconversion of Ureas Finally, areas may be further manipulated using methods familiar to those skilled in the art.
The compounds may be administered orally, . topically, parenterally, by 10 inhalation or spray or vaginally, sublingually, or rectally in dosage trait formulations.
The term 'administration by injection' includes intravenous, iritramuscular, subcutaneous and parenteral injections, as well as use of infusion techniques.
Dermal administration may include topical application or transdermal administration.
One or more compounds rnay be present in association with one or more non-toxic pharmaceutically acceptable carriers and if desired other active ingredients.
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 rnay 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, microcrystalline cellulose, carboxymethyl cellulose, hydroxypropylmethylcellulose or alginic acid; and binding agents, for example magnesium stearate, stearic acid or talc . and lubricants/surfactants such as sodium lauryl sulfate. 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.
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.
Aqueous suspensions contain the active materials in admixture with excipients suitable for the manufacture of aqueous suspensions. Such excipients are suspending agents, for example sodium oarboxymethylcellulose, 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 or an alkylene oxide with fatty acids, for example polyoxyethylene stearate, or condensation products of ethylene oxide with long chain aliphatic alcohols, for example ~heptadecaethylene oxycetanol, 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.
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.
The compounds rnay 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.
Pharmaceutical compositions of the invention may also be in the form of oil-in-water emulsions. The oily 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-occurnng 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, fox example polyoxyethylene sorbitan monooleate. The emulsions may also contain sweetening and flavoring agents.
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.
The compounds may also be administered in the form of suppositories fox rectal or vaginal administration of the drug. These compositions can be prepared by mixing the drug with a suitable non-irntating 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.
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.
W094104157 3Mar94). 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.
Suitable solvents for processing transdermal delivery systems axe known to those skilled in the art, and include lower alcohols~ such as ethanol or isopropyl alcohol, lower ketones uch 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 dichloxomethane, 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.
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 ~br benzyl alcohol, saturated or unsaturated C$-C1$ fatty alcohols such, as Iauryl alcohol or cetyl alcohol, saturated or - unsaturated C8-C~8 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 palrnitic 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 furnarate.
Additional penetration enhancing materials include phosphatidyl derivatives such as lecithin or cephalin, terpenes, amides, ketones, areas 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 C8-Ci~ fatty alcohols; 'saturated or unsaturated C8-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, areas and their derivatives, and ethers.
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.

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 5 , 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/I~.g of total body weight. The daily rectal dosage regime will preferably be from 0.01 to 200 mg/I~g of total body weight.
The daily topical dosage regime will . preferably be from 0.1 to 200 mg administered between one to four times daily. The transdermal concentration will preferably be that 10 required to maintain a daily dose of ~ from 0.01 to 200 mg/Kg. The daily inhalation dosage regime will preferably be from 0.01 to 10 mg/Kg of total bady weight.
These dosages regimes ,can be achieved with multiple dosages within a single day or extended dosages, such as those given on a weekly or monthly basis.
15 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 appreciated by one skilled in the art that the specific dose level for any given patient will depend upon a variety of factors, including, the activity of the ~ specific compound employed, the age of the 20 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 combinations, and the severity of the condition undergoing therapy.
It will be further appreciated by one skilled in the art that the optimal course of 25 treatment, i.e., the mode of treatment and the daily number of doses of a compound of this invention given for a defined number of days, can be ascertained by those skilled in the art using conventional treatment tests.
It will be understood, however, that the specific dose level for any particular 30 patient will depend upon a variety of factors, including the activity of the specific compound employed, the age, body weight, general health, sex, diet, time of administration, route of administration, and rate of excretion, drug combination and the severity of the condition undergoing therapy.
Specific preparations of the compounds of this invention are already described in the patent literature, and can be adapted to the compounds of the present invention. For example, Miller S. et al, "Inhibition of p38 Kinase using Symmetrical and Unsymmetrical biphenyl Ureas" PCT Int. Appl. WO 99 32463, Miller, S et al.
"Inhibition of raf Kinase using Symmetrical and Unsymmetrical Substituted biphenyl Ureas" PCT Int. Appl., WO 99 32436, Dumas, J. et al., "Inhibition of p38 Kinase Activity using Substituted Heterocyclic Ureas" PCT Int. Appl., WO 99 32111, Dumas, J. et al., "Inhibition of RAF I~inase Activity using Substituted Heterocyclic Ureas" PCT Int. Appl., WO 99 32106, Dumas, J. et al., "Method for the Treatment, of Neoplasm by Inhibition of raf Kinase using N-Heteroaryl-N'-(hetero)arylureas"
PCT
Int. Appl., WO 99 32106, Dumas, J. et al., "Inhibition of p38 Kinase Activity using Aryl- and Heteroaryl- Substituted Heterocyclic Ureas" PCT Int. Appl., WO 99 32110, Dumas, J., et al., "Inhibition of raf Kinase using Aryl- and Heteroaryl-Substituted Heterocyclic Ureas" PCT Int. Appl., WO 99 32455, Riedl, B., et al., "O-Carboxy Aryl Substituted biphenyl Ureas as raf Kinase Tnhibitors" PCT Int. ~
Appl., WO 00 42012, Riedl, B., et al., "O-Carboxy Aryl Substituted biphenyl Ureas as p38 I~inase Inhibitors". PCT Int. Appl., WO 00 41698. ' Methods for preparaing the compounds of this' invention are also described in the following U.S. applications, some of which correspond to the PCT
.applications listed above.
08/863,022', filed May 23, 1997;
~ 08/996,344, filed December 22, 1997;
08/996,343, filed December 22, 1997;
08/996,181, filed December 22, 1-997;
08/995,749, filed December 22, 1997;
08/995,750, filed December 22, 1997;
08/995,751, filed December 22, 1997;
09/083,399, filed May 22, 1998;
09/425,228, f led October 22, 1999;

09/777,920, fled February 7, 2001.
09/722,418 filed November 28, 2000 09/838,285, filed April 20, 2001;
09/838,286, filed April'20, 2001;
09/458,548, filed January 12, 2001;
09/948,915, filed September 10, 2001, and Serial Number (attorney docket number: Bayer 34 Vl), filed December 3, 2001.
The entire disclosure of all applications, patents and publications cited above and below are hereby incorporated by reference.
.
The compounds of this invention axe producible from known compounds (or from; starting materials which, in turn, are producible from known compounds), e.g., through the general preparative methods shown below. The activity of a given compound to inhibit angiogenesis activity can be routinely assayed, e.g., according to procedures disclosed below.
Without further elaboration, it is believed that one skilled in the art can, using the preceding description, utilize the present invention to its fullest extent. The following examples are, therefore, to be construed as merely illustrative and not lirilitative of the remainder of the disclosure in any way whatsoever. 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
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 approxirriately 15 mmHg.

All temperatures are reported uncorrected in degrees Celsius (°C).
Unless otherwise indicated,. all parts and percentages axe by weight.
Commercial grade reagents and solvents were used without further purification.
Thin-layer chromatography (TLC) was performed on. Whatman~ pre-coated glass-backed silica gel 60A F-254 250 N.m 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-dinitrophenylhydiazine followed by heating. Column chromatography (flash chromatography) was performed using 230=400 mesh EM Science° silica gel.
Melting points (mp) were determined, using a Thomas-Hoover melting point apparatus or a Mettler FP66~ automated melting point apparatus and are uncorrected.
Proton (1H) nuclear magnetic resonance (NMR) spectra were measured with a General Electric GN-Omega 300 (300 MHz) spectrometer with either MeøSi (8 0.00) or residual protonated solvent (CHCl3 8 7.26; MeOH 8 3.30; DMSO 8 2.49) as standard.
Carbon (13C) NMR spectra were measured with a General Electric GN-Omega 300 (75 MHz) spectrometer with solvent (CDC13 8 77.0; MeOD-d3; & 49.0; DMSO-d6 8 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 bombardrzient (FAB) mass spectra. Electron impact mass spectra (EI-MS) were obtained with a Hewlett Packard 59~9A 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 ~,A. Liquid-cesium secondary ion mass spectra (FAB-MS), an updated version of fast atom bombardment were obtained using a I~ratos Concept 1-H spectrometer.

Chemical ionization mass spectra (CI-MS) were obtained using a Hewlett Packard MS-Engine (5989A) with methane as the reagent gas (1x10-ø tort to 2.5x10-4 tort). The direct insertion desorption chemical ionization (DCI) probe (Vaccumetrics, Inc.) was tamped from 0-1.5 amps in 10 sec and held at 10 amps until all traces of the sample disappeared ( N1-2 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 axnu 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 chrorriatograph equipped with an HP-I methyl silicone column (0.33 mM coating; 25 m x 0.2 mm) and a Hewlett Packard.5971 Mass Selective Detector (ionization energy 70 eV).
Elemental analyses were conducted by Robertson Microlit Labs, Madison NJ.
All compounds displayed NMR spectra, LRMS and either elemental analysis or HRMS consistent with assigned structures.
List of Abbreviations and Acronyms:
AcOH acetic 'acid anh ~ anhydrous BOC test-butoxycarbonyl conc ~ concentrated dec decomposition J
DMPU ~ 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone DMF N,N .dimethylformamide DMSO dimethylsulfoxide 30. DPPA diphenylphosphoryl azide~
EtOAc ethyl acetate EtOH ethanol (100%) Et20 diethyl ether Et3N triethylamine m-CPBA 3-chloroperoxybenzoic acid MeOH methanol 5 pet. ether ~ petroleum ether (boiling range 30-60 °C) THF tetrahydrofuran TFA trifluoroacetic acid Tf trifluoromethanesulfonyl EXAn~IPLE A
N-[4-chloro-3-(trifluoromethyl)phenyl]-N'- ~4-.[2-carbamoyl-(4-yridyloxy)]phenyl'~ urea . ' I S Step 1: Preparation of 4-chloro-2-pyridinecarboxamide CI -N NHZ
O
To a stirred mixture of methyl 4-chloro-2-pyridinecarboxylate hydrochloride (1.0 g, 4.81 mmol) dissolved in cone. aqueous ammonia (32 mL) v~ras added ammonium chloride (96.2 mg, 1.8 mmol, 0.37 equiv.), and the heterogeneous reaction mixture was stirred at ambient-temperatuxe for 16h. The reaction mixture was poured into EtOAc (500 mL) and water (300 mL). The organic layer was washed with water (2 x 300 mL) and a saturated NaCl solution (l x 300 mL), dried (MgS04), concentrated in vacuo to give 4-chloro-2-pyridinecarboxamide as a beige solid (604.3 mg, 80.3%):_TLC (50%.EtOAc / hexane) Rf 0.20; 1H-NMR (DMSO-d6) S 8.61 (d, J =
5.4 Hz, 1H), 8.20 (broad s, 1H), 8.02 (d, J = 1.8 Hz, 1H), 7.81 (broad s, 1H), 7.76 to 7.73 (m, 1H). ~ _ Step 2: Preparation of 4-(4-aminophenoxy)-2-pyridinecarboxamide O
NHS
HZN / i N
To 4-aminophenol (418 mg, 3.83 rnmol) in anh DMF(7.7 mL) was added' potassium text-butoxide (447 mg, 3.98, mrnol, 1.04 equiv.) in one portion. The reaction mixture was stirred at room temperature for 2 h, and a solution of 4-chloro-2-pyridinecarboxamide (600 mg, 3.83 mmol, 1.0 equiv.) in anh DMF (4 mL) was then added. The reaction mixture was stirred at 80 °C for 3 days and poured into a mixture of EtOAc and a saturated NaCI solution. The organic layer was sequentially washed with a saturated NH4Cl solution then a~ saturated NaCl solution, dried (MgS04), and concentrated under reduced.pressure. The crude product was purified using MPLC
chromatography (Biotage~; gradient from 100% EtOAc to followed by 10% MeOH /
50% EtOAc / 40% hexane) to give the 4-chloro-5-trifluoromethylaniline as a brown solid (510 mg, 58%). 1H-NMR (DMSO-d6). d 8.43 (d, J = 5,.7 Hz, 1H), 8.07 (br s, 1H), 7.66 (br s, 1H), 7.31 (d, J = 2.7 Hz, 1H), 7.07 (dd, J = 5.7 Hz, 2:7 Hz, 1H),
6.85 (d, J =
9.0 Hz, 2 H), 6.62 (d, J = 8.7 Hz, 2H), 5.17 (broad s, 2H); HPLC EI-MS rnlz ((M+H)+. , Step 3: Preparation of N-[4-chloro-3-(trifluoromethyl)phenyl]-N'-~4-[2-carbamoyl-(4-pyridyloxy)]phenyl} urea w O
FI ~ ~ O. f ~ O ~ ~ NH2 .
F / ~ ~ iN
~N N
I I
F H H
A mixture . of 4-chloro-5-trifluoromethylaniline (451 rng, 2.31 mmol, 1.1 equiv.) and 1,1'-carbonyl diimidazole (419 mg, 2.54 mmol, .l .2 equiv.) in anh dichloroethane (5.5 mL) was stirred under argon at 65 °C for 16 h. Once cooled to room temperature, a solution of 4-(4-aminophenoxy)-2-pyridinecarboxamide (480 mg, 2.09 mmol) in anh THF (4.0 mL) was added, and the reaction mixture Was stirred at 60°C for 4 h. The reaction mixture was poured into EtOAc, and the organic layer was washed with water (2x) and a saturated NaCl solution (lx), dried (MgSOø), filtered, and evaporated in vacuo. Purification using MPLC chromatography (Biotage~;
gradient from , 100% EtOAc to 2% MeOH l EtOAc) gave N-[4-chloro-3-(trifluoromethyl)phenyl]-N'-{4-[2-carbamoyl-(4-pyridyloxy)]phenyl} urea as a ,white solid' (770 mg, 82%): TLC (EtOAc) Rr 0.1 l, 100% ethyl acetate ~H-NMR (DMSO-d6) 8 9.2I (s, IH), 8.99 (s, 1H), 8.50 (d, J = 5.6 Hz, 1H), 8.11 (s, 1H), 8.10 (s, 1H), 7.69 (broad s, 1H), 7.64 (dd, J = 8.2 Hz, 2.I Hz, IH), 7.61 (s, 1H), 7.59 (d, J =
8.8 Hz, 2H),
7.39 ~ (d, J = 2.5 Hz, 1H), 7.15 (d, J = 8.9 Hz, 2H), 7.14 (m, 1H); MS LC-MS
(MHO _ 451). Anal. calcd fox CZOHIøC1F3N403: C 53.29% H 3.13% N 12.43%. Found: C
~ 53.33% H 3.21% N 12.60%;.
Example B
N-[4-chloro-3-(trifluoromethyl)phenyl]-N'- ~4-[2-N-methylcarbamoyl-4-.o FI I ~ O ~ ~ O ~ ~ NHCH3 F / ~ ~ rN
~N N
f I
pyridyloxy]phenyl} urea F ~ H H
Step 1: 4-Chloro-N methyl-2-pyridinecarboxamide is first synthesized from 4-chloropyridine-2-carbonyl chloride by adding 4-chloropyridine-2-carbonyl chloride HCl salt (7.0 g, 32.95 mmol) in portions to a mixture of a 2.0 M methylamine solution in THF (100 mL) and MeOH (20 mL) at 0 °C. The resulting mixture is stored at 3 °C
for 4 h, then concentrated under reduced pressure. The resulting nearly dry solids are suspended in EtOAc (I00 mL) and filtered: The fltrate is washed with a saturated NaCl solution (2 x 100 mL), dried (NaZS04) and concentrated under reduced pressure to provide 4-chloro-N methyl-2-pyridinecarboxamide as. a yellow, crystalline solid.
Step 2: A solution of 4-aminophenol (9.60 g, 88.0 mmol) in anh. pMF (150 mL) is treated with potassium text-butoxide (10.29 g, 91.7 mmol), and the reddish-brown mixture is stirred~at room temp, for 2 h. The contents are treated with 4-chloro-N
methyl-2-pyridinecarboxamide (15.0 g, 87.9 mmol) from Step l and K2CO3 (6.50 g, 47.0 mmol) and then heated at 80 °C for 8 h. The mixture is cooled to room temp.
and separated between EtOAc (500 mL) and a saturated NaCI solution (500 mL).
The aqueous ,phase is back-extracted with EtOAc (300 mL). The combined organic layers are washed with a saturated NaCl solution (4 x 1000 mL), dried (NazSOø) and concentrated under reduced pressure. The resulting solids are dried under reduced
8 PCT/US03/04103 pressuxe at 3S °C for 3 h to afford 4-(2-(N methylcarbamoyl)-4-pyridyloxy)aniline as a light-brown solid. ~H=NMR (DMSO-d6) S 2.77 (d, J--4.8 Hz, 3H), 5.17 (br s, 2H), 6.64, 6.86 (AA.'BB' quartet, J 8.4 Hz, 4H), 7.06 (dd, J--S.S, 2.S Hz, 1H), 7.33 (d, J--2.S Hz, 1H), 8.44 (d, J--S.S Hz, 1H), 8.73 (br d, 1H); HPLC ES-MS m/z 244 ((M+H)+).
Step 3: A solution of 4-chloro-3-(trifluoromethyl)p~enyl isocyanate (14.60 g, 65.90 mmol) in CH2C12 (3S mL) is added -dropwise to a suspension of 4-(2-(N
methylcarbamoyl)-4-pyridyloxy)aniline from Step 2; (16.0 g, 6S.77 mrnol) in ~ (3S mL) at 0 ~°C. The resulting mixture is stirred at room temp. for 22 h. The resulting yellow solids are removed by filtration, then washed with CH2Cl2 (2 x 30 mL) and dried under reduced pressure (approximately 1 mmHg) to afford N (4-chloro-3-(trifluoromethyl)phenyl)-N'-(4-(2-(N methylcarbamoyl)-4-pyridyloxy)phenyl) urea as an off white solid: mp 207-209 °C; 1H-NMR (DMSO-d6) 6 2.77 (d, J--4.8 Hz, 3H), 1S 7.16 (m, 3H), 7.37 (d, J--2.S Hz, 1H); 7.62 (m, 4H), 8.11 (d, .I--2.S Hz, 1H), 8.49 (d, J--S.S Hz, 1H), 8.77 (br d, 1H), 8.99 (s, 1H), 9.21 (s, 1H); HPLC ES-MS mlz ((M+H)+).
Example C
N-[2-methoxy-S-(trifluoromethyl)phenyl]-N'- f 4-[2-N-methylcarbamoyl-4-pyridyloxy]phenyl} urea , ~H3 ' O , O O ~ O ~ NHCH3 , F ~ ~ N~N ~ ~ ~ i N
I I
F H N
2S Step 1: 4-Chloro-N methyl-2-pyridinecarboxamide ~ is first synthesized from chloropyridine-2-carbonyl chloride by adding 4-chloropyridine-2-carbonyl chloride HCI salt (7.0 g, 32.95 mmol) in portions to a mixture of a 2.0 M methylamine solution in THF (100 mL) and MeOH (20 mL) at 0 °C. The resulting, mixture is stored at 3 °C
for 4 h, then concentrated under reduced pressure. The resulting nearly dry solids are.

suspended in EtOAc (100 mL) and filtered. The filtrate is washed with a saturated NaCl solution (2 x 100 mL), dried (NazS04) and concentrated under reduced pressure to provide 4-chloro-N methyl-2-pyridinecarboxamide as a yellow, crystalline solid.
S Step 2: A solution of 4-aminophenol (9.60 g, 88.0 mmol) in anh. DMF (150 mL) is _ treated with potassium tart-butoxide (10.29 g, 9I.7 mmol), and the reddish-brown mixture is stirred at room temp. for 2 h. The contents are treated with 4-chloro-N
methyl-2-pyridinecarboxamide (15.0 g, 87.9 mmol) from Step 1 and KZC03 (6.50 g, 47.0 mmol) and then heated at 80 °C for.8 h. The mixture is cooled to room temp.
and separated between EtOAc (500 mL) and a saturated NaCl solution (S00 mL).
The aqueous phase is back-extracted with EtOAc (300 mL). " The combined organic layers are washed with a saturated NaCl solution (4 x 1000 mL), dried (NaZS04) and concentrated under reduced pressure. The resulting solids are dried under reduced pressure at 35 °C for 3 h to afford 4.-(2-(N methylcarbamoyl)-4-pyridyloxy)anilirie as a light-brown solid. 1H-NMR (DMSO-d6) ~ 2.77 (d, J--4.8 Hz, 3H), 5.17 (br s, 2H), 6.64, 6.86 (AA'BB' quartet, J--8.4 Hz, 4H); 7.06 (dd, J--5.5, 2.5 Hz, 1H), 7.33 (d, J--2.5 Hz, 1H), 8.44 (d, J--5.5 Hz, 1H), 8.73 (br d, 1H); HPLC ES-MS m/z 2,44 ((M+H)+). :
Step 3: To a solution of 2-methoxy-5-(trifluoromethyl)aniline (0.15 g) in anh CH2Cl2 (15 mL) at 0 °C is added CDI (0.13 g). The resulting solution is allowed to warm to room temp. over 1 h, is stirred at room temp. for 16 h, then is treated with 4-(2-(N
methylcarbamoyl)-4-pyridyloxy)aniline (0.18 g) from Step 2. The resulting yellow solution is stirred at room temp.' for 72 h, then is treated with HZO (125 mL). The resulting aqueous mixture is extracted with EtOAc (2 x 150 mL). The combined organics -are washed with a saturated NaCI solution (100 mL), dried (MgS04) and concentrated under reduced pressure. The residue is triturated (90% EtOAc/10%
hexane). The resulting white solids are collected by filtration and washed.
with .
EtOAc. The filtrate is concentrated under reduced pressure and the residual oil purified by column chromatography (gradient from 33% EtOAc/67% hexane to 50%
EtOAc/50% hexane to 100% EtOAc) to give N (2-methoxy-5-(trifluoromethyl)phenyl)-N'-(4-(2-(N methylcarbamoyl)-4-pyridyloxy)phenyl) urea as a light tari solid: TLC (100% EtOAc) R~ 0.62; 1H NMR (DMSO-d6) 8 2.76 (d, J--4.8 Hz, 3H), 3.96 (s, 3H), 7.1-7.6 and 8.4-8.6 (m, 11H), 8.75 (d, J 4.8 Hz, 1H),
9.55 (s, 1 H); FAB-MS rnlz 461 ((M+H)+).

KDR (VEGFR2) Assay The cytasolic kinase domain of KDR kinase was expressed as a 6His fusion protein in S~ insect cells. The I~DR kinase domain fusion protein was purified over a
10 Ni++ chelating column. Ninety-six well ELISA plates were coated with 5 ~l HEPES
buffer (20 mM poly(Glu4;Tyr1) (Sigma Chemical Co., St. Louis, MO) in 100 ~,k HEPES buffer (20 mM HEPES, pH 7.5, 150 mM Na Cl, 0.02% Thimerosal) at 4°
overnight. Before use, the plate was washed with HEPES, NaCI buffer and the plates were blocked with 1% BSA, 0.1% Tween 20 in HEPES, NaCl buffer.
15 Test compounds were serially diluted in 100% DMSO form 4 mM to 0.12 ~,M
in half log dilutions. These dilutions were further diluted twenty fold in H20 to obtain compound solutions in 5% DMSO. Following loading of the assay plate with 85 ~l of assay buffer (20 mM HEPES, pH 7.5, 100 mM ICI, 10 xnM MgCl2, 3 mM
MnCl2, 0.05% glycerol, 0.005% Triton X-100, 1 mM -mercaptoethanol, with or 20 without 3.3 ~M ATP), 5 ~.I of the diluted compounds were added to a final assay volume of 100 ~.1. Final concentrations were between 10 p.M, and 0.3 mM in 0.25%
DMSO. The assay was initiated by the addition of 10,1 (30~ ng) of KI7R kinase domain.
25 The assay was incubated with test cornpourld or vehicle alone with gentle agitation at room temperature for 60 minutes. The wells were washed and phosphotyrosines (PY) were probed with ari anti-phosphotyrosine (PY), mAb clone 4610 (Upstate Biotechnology, Lake Placid, NY). PY/anti-PY complexes were detected with an anti-mouse IgG/I3RP conjugate Iamersham International plc, 30 Buckinghamshire, England). Phosphotyrosine was quantitated by incubating with '100 ~,l 3, 3', 5, 5' tetramethylbenzidine solution (Kirkegaard and Perry, TMB
Microwell 1 Component peroxidase substrate). Color development was arrested by the addition of . . ~ 41 100 ~,l 1% HCl-based stop solution (Kirkegaard and Perry, TMB 1 Component Stop Solution).
Optical densities were determined spectrophotometrically at 450 nm in a 96-well plate reader, SpectraMax 250 (Molecular Devices). Background (no ATP in assay) OD values were subtracted from all Ods and the percent inhibition was calculated according to the equation:
Inhibition = (OD(vehicle controll - OD (with compound) X 100 OD (vehicle control) - OD (no ATP added) The ICSO values were determined with a least squares analysis program using compound concentration versus percent inhibition.
The following compounds were tested in the assay described above and were found to have either an ICSO of less than 10 micromolar or showed greater than 30%
inhibition at 1 micromolar. Compound names were generated using NomenclatorTM v 3.0 and may differ from those in the patent applications.
From WO 1999/32463:
Entry Name No I

73 N-[5-(tert-butyl)-2-(3-thienyl)phenyl][(4-(4-w pyridyloxy)phenyl)amino]carboxamide 96 ~[4-(4-methoxyphenoxy)phenyl]amino]-N-[2-methoxy-5-(trifluoromethyl)phenyl]carboxamide 99 N-[2-methoxy-5-(trifluoromethyl)phenyl][(3-(4-pyridylthio)phenyl)amino]carboxamide 100 N-[2-methoxy-5-(trifluoromethyl)phenyl][(3-(4-pyridylthio)phenyl)amino]carboxarnide 101 N-[2-methoxy-5-(trifluoromethyl)phenyl] [(4-(4-pyridyloxy)pheriyl)amino]carboxamide From WO 1999/32436:

Entry Name No
11 N-[5-(tert-butyl)-2-methoxyphenyl][(3-(4-pyridylthio)phenyl)amino]caxboxamide
12 N-[5-(tert-butyl)-2-(3-thienyl)phenyl][(4-(4-pyridyloxy)phenyl)amino]carboxamide 17 N-[3-(tent-butyl)phenyl][(4-(4-. , pyridyloxy)phenyl')amirio] carboxamide 23 {[3-(tert-butyl)phenyl]amino-N-(4-(3-pyridyl)phenyl)c arboxamide 33 {[4-(4-methoxyphenoxy)phenyl]amino}-N-[2-methoxy-5-(trifluoromethyl)phenyl] carboxamide 36 N-[2-methoxy-5-(trifluoromethyl)phenyl][(3-(4-pyridylthio)phenyl)amino] carboxamide 37 N-[2-methoxy-5-(trifluoromethyl)phenyl][(3-(4-pyridylthio)phenyl)amino] carboxamide 38 N-[2-methoxy-5-(trifluoromethyl)phenyl][(4-(4-pyridyloxy)phenyl)amino]carboxamide 56 N-[2-methoxy-5-(trifluoromethyl)phenyl] {[3-(2-methyl(4-pyridyloxy))phenyl] amino ~ c arboxamide 70 [.(3-chloro-4-(6-quinolyloxy)phenyl)amino]-N-[2-methoxy-5-(trifluoromethyl)phenyl]carboxamide 81 ' [(4-(4-pyridyloxy)phenyl)amino]-N-[3-(trifluoromethyl)phenyl]carboxamide 82 N-[2-chloro-5.-(trifluoromethyl)phenyl] [(4-(4-pyridyloxy)phenyl)amino]carboxamide 83 N-[2-fluoro-5-(trifluoromethyl)phenyl] [(4-(4-pyridyloxy)phenyl)amino]carboxamide 91 {[4-chloro-3-(trifluoromethyl)phenyl]amino]-N-(2-methyl-4-(3-pyridyloxy)phenyl)carboxamide 102 N-[4-chloro-3-(trifluoromethyl)phenyl] [(4-(4-pyridyloxy)phenyl)amino] carboxamide 103 N-[4-chloro-3-(trifluoromethyl)phenyl] {[4-(4-methoxyphenoxy)phenyl] amino } carboxamide 105 ~[4-chloro-3-(trifluoromethyl)phenyl]amino}-N-[3-(4-pyridylcarbonyl)phenyl]carboxamide 106 f [4-chloro-3-(trifluoromethyl)phenyl]amino}-N-[3-(2-methyl(4-pyridyloxy))phenyl]carboxamide 119 N-[4-fluoro-3-(trifluoromethyl)phenyl] [(4-(4-pyridyloxy)phenyl)amino]carboxamide 132 N-[4-chloro-2-methoxy-5-(trifluoromethyl)phenyl][(4-{4-pyridyloxy)phenyl)amino] carboxamide 133 N-[5-methoxy-3-(trifluoromethyl)phenyl][(4-(4-pyridyloxy)phenyl)amino]carboxamide 135 [(3-bromo-4-chlorophenyl)amino]-N-(4-{4-pyridyloxy)phenyl)carboxamide 136 [(4-(4-pyridyloxy)phenyl)amino]-N-[3-(trifluoromethoxy)phenyl]carboxamide 141 . N-[3,5-bis(trifluoromethyl)phenyl][(4-(4-pyridyloxy)phenyl)amino]carboxamide From WO 1999/32111:
Entry Name No 18 N-[5-(tent-butyl)isoxazol-3-yl][(4-(4-pyridylthio)phenyl)amino~carboxamide .

32 f [5-(tert-butyl)isoxazol-3-yl]amino}-N-(3-(4-pyridylthio)phenyl)carboxamide 53 N-[5-(tent-butyl)isoxazol-3-yl][(4-(4-pyridyloxy)phenyl)amino] carboxamide 59 N-[5-(tert-butyl)isoxazol-3-yl] [(4-(3-pyridyloxy)phenyl)arnino]carboxamide 67 f 3-[4-(~[5-(tert-butyl)isoxazol-3-yl] amino} carbonylamino)phenoxy]phenyl} -N-methylcarboxamide 85 ~[5-(tert-butyl)isoxazol-3-yl]amino}-N-[3-(2-methyl(4-pyridyloxy))phenyl]carboxamide 86 N-[5-(tert-butyl)isoxazol-3-yl] ~[4-(2-methyl(4-pyridyloxy))phenyl] amino} carboxamide 103 4-[4-({[5-(tert-butyl)isoxazol-3-yl] amino} carbonylamino)phenoxy]pyridine-2-carboxamide 104 ~[5-(tert-butyl)isoxazol-3-yl]amino}-N-~3-[2-(N-methylcarbamoyl)(4-pyridyloxy)]phenyl} carboxamide 105 4-[3-(~N-[5-(tert-butyl)isoxazol-3-yl]carbamoyl} amino)phenoxy]pyridine-2-carboxarnide 106 3-[4-(~[5-(tert-butyl)isoxazol-3-yl] amino } carbonylamino)phenoxy]benzamide 143 N-[3-(methylethyl)isoxazol-5-yl] [(4-(4-pyridyloxy)phenyl)amino]carboxamide 146 N-(3-cyclobutylisoxazol-5-yl)[(4-(4-pyridyloxy)phenyl)amino] carboxamide 147 N-(3-cyclobutylisoxazol-5-yl)[(4-(6-quinolyloxy)phenyl)amino]carboxamide 162 ~[3-(tert-butyl)isoxazol-5-yl]amino}-N-(3-(4-pyridylthio)phenyl)carboxamide 163 N-[3-(tent-butyl)isoxazol-5-yl][(4-(4-pyridyloxy)phenyl)amino]carboxamide 164 N-[3-(tent-butyl)isoxazol-5-yl] ~[4-(4-methoxyphenoxy)phenyl] amino} carboxamide 188 N-[3-(1,1-dimethylpropyl)isoxazol-5-yl][(3-(4-pyridylthio)phenyl)amino]carboxamide 195 N-[3-(1,1-dimethylpropyl)isoxazol-5-yl][(4-(4-pyridyloxy)phenyl)amino] carboxamide 220 {[3-(tent-butyl)pyrazol-5-yl]amino}-N-(3-(4-pyridylthio)phenyl)carboxamide 221 N-[3-(tent-butyl)pyrazol-S-yl][(4-(4-pyridylthio)phenyl)amino]carboxamide 222 {3-[4-({[3-(tent-butyl)pyrazol-5-yl] amino } carbonylamino)phenoxy]phenyl }
-N-methylcarboxamide, 2,2,2-trifluoroacetic acid 225 N-[3-(tert-butyl)-1-methylpyrazol-5-yl][(3-(4-pyridylthio)phenyl)amino]carboxamide 251 N-[3-(tent-butyl)-1-methylpyrazol-5-yl][(4-(4-pyridyloxy)phenyl)amino]carboxamide 261 N-[3-(tert-butyl)-1-methylpyrazol-5-yl] {[4-(4-pyridylmethyl)phenyl] amino } carboxamide 266 N-[3-(tert-butyl)-1-methylpyrazol-5-yl] {[4-(4-pyridylmethoxy)phenyl] amino } carboxamide 277 tert-butyl 3-(tert-butyl)-5-[( {4-[3-(N-methylcarbamoyl)phenoxy]phenyl} amino)carbonylamino]pyraz olecarboxylate 280 N-[5-(tent-butyl)(1,3,4-thiadiazol-2-yl)][(4-(4-pyridyloxy)phenyl)amino]carboxamide 281 {[5-(tent-butyl)(1,3,4-thiadiazol-2-yl)]amino}-N-(3-(4-pyridylthio)phenyl)carboxamide 284. N-[5-(tert-butyl)(3-thienyl)][(4-(3-pyridyloxy)phenyl)amino]carboxamide 293 N-[5-(tert-butyl)(3-thienyl)][(4-(4-pyridyloxy)phenyl)amino]carboxamide 299 N-(6-chloro(1H-indazol-3-yl))[(4-(4-pyridyloxy)phenyl)amino]carboxamide 302. (~4-[2-(N-methylcarbamoyl)(4-pyridyloxy)]phenyl'~amino)-N-(1-methyl-3-phenylpyrazol-5-yl)carboxamide From WO 1999/
Entry Name , No 21 N-[5-(tert-butyl)isoxazol-3-yl][(4-(4-pyridylthio)phenyl)amino]carboxamide 42 {[5-(tert-butyl)isoxazol-3-yl]amino}-N-(3-(4-pyridylthio)phenyl)carboxamide 59 N-[5-(tert-butyl)isoxazoh3-yl][(4-(4-.

pyridyloxy)phenyl)amino]carboxamide .

64 N-[5-(tert-butyl)isoxazol-3-yl][(4-(3-pyridyloxy')phenyl)amino]carboxamide 69 f 3-[4-{ f [5-(tent-butyl)isoxazol-3-yl]amino} carbonylamino)phenoxy]phenyl}-N-methylcarboxamide 81 ~[~-(tent-butyl)isoxazol-3-yl]amino}-N-[3-(2-methyl(4-pyridyloxy))phenyl]carboxamide 82 N-[5-(tert-butyl)isoxazol-3-yl] f [4-(2-methyl(4-pyridyloxy))phenyl] amino } c arboxamide 1 O1 {4-[4-( ~ [5-(tent-butyl)isoxazol-3-yl] amino ~ c arbonylamino)pherioxy] (2-pyri~dyl) } -N-methylcarboxamide 103 4-[4-( f [5-(tert-butyl)isoxazol-3-yl] amino } carbonylamino)phenoxy]pyridine-2-carboxamide 104 4-[3-( {N-[5-(tert-butyl)isoxazol-3-yl]carbamoyl} amino)phenoxy]pyridine-2-carboxamide 105 {[5-(tert-butyl)isoxazol-3-yl]amino}-N-~3-[2-(N-methylcarbamoyl)(4-pyridyloxy)]phenyl} carboxamide 106 3-[4-(([5-(tert-butyl)isoxazol-3- .

yl] amino} carbonylamino)phenoxy]benzamide 118 f4-[4-({[5-(tent-butyl)isoxazol-3-yl]amino}carbonylamino)-3-chlorophenoxy] (2-pyridyl) } -N-methylcarboxamide 124 {3-[4-({[5-(tert-butyl)isoxazol-3-yl] amino } c arbonylamino)phenoxy]phenyl } -N-(2-morpholin-4-ylethyl)carboxamide 125 {4-[4-({[5-(tent-butyl)isoxazol-3-yl] amino } c arbonylamino)phenoxy] (2-pyridyl) } -N-ethylcarboxamide 126 {4-[4-({[5-(tent-butyl)isoxazol-3-yl]amino}carbonylamino)-2-chlorophenoxy](2-pyridyl)}-N-methylcarboxamide 127 {[5-(tert-butyl)isoxazol-3-yl]amino}-N-{2-methyl-4-[2-(N-methylcarbamoyl)(4-pyridyloxy)]phenyl} carboxamide 128 {[5-(tent-butyl)isoxazol-3-yl]amino} -N-{3-[2-(N-methylcarbamoyl)(4-pyridylthio)]phenyl} carboxamide 130 ~ {3-[4.-({[5-(tent-butyl)isoxazol-3-yl]amino} carbonylamino)phenoxy]phenyl}-N-(3-pyridyl)carboxamide 140 {4-[4-({[5-(tert-butyl)isoxazol-3-yl] amino} carbonylamino)phenylthio] (2-pyridyl)}-N-methylcarboxamide 182 N-methyl{4-[4-({[3-(methylethyl)isoxazol-5-yl]amino}carbonylamino)phenoxy](2-pyridyl)}carboxamide 186 N-methyl {4-[3-( { [3-(methylethyl)isoxazol-5-yl] amino} carbonylamino)phenoxy] (2-pyridyl)}
carboxamide 187 N-(3-cyclobutylisoxazol-5-yl)[(4-(6-quinolyloxy)phenyl)amino]carboxamide 188 N-(3-cyclobutylisoxazol-5-yl)[(4-(4-pyridyloxy)phenyl)amino]carboxamide 194 N-[3-(tert-butyl)isoxazol-5-yl][(4-(4-pyridyloxy)phenyl)amino] carboxamide 195 N-[3-(tent-butyl)isoxazol-5-yl] {[4-(4-methoxyphenoxy)phenyl] amino} carboxamide 206 {[3-(tert-butyl)isoxazol-5-yl]amino}-N-(3-(4-pyridylthio)phenyl)carboxamide 212 N-[3-(tart-butyl)isoxazol-5-yl] {[4-(1,3-dioxoisoindolin-5-yloxy)phenyl]amino} carboxamide 213 {[3-(tart-butyl)isoxazol-5-yI]amino}-N-[4-(1-oxoisoindolin-5-yloxy)phenyl] c arb oxamide 214 {4-[4-({[3-(tart-butyl)isoxazol-5-yl]amino}carbonylamino)phenoxy](2-pyridyl)}-N-, ethylcarboxamide 215 {4-[4-({[3-(tart-butyl)isoxazol-5-yl]amino}carbonylamino)-2-chlorophenoxy](2-pyridyl)}-N-methylcarboxamide 216. {[3-(tart-butyl)isoxazol-S-yl]amino}-N-{3-[2-(N-methylcarbamoyl)(4-pyridylthio)]phenyl} carboxamide 2I7 {4-[4-({[3-(tart-butyl)isoxazol-5-yl]amino} carbonylamino)phenylthio] (2-pyridyl)}-N-methylcarboxamide 218 {4-[4-({[3-(tart-butyl)isoxazol-5-yl]amino}carbonylamino)phenoxy](2-pyridyl)}-N-' methylcarboxamide 228 {[3-(tart-butyl)isoxazol-5-yl]amino}-N-[3~(6-methyl(3-pyridyloxy))phenyl]carboxamide 240 N-[3-(tart-butyl)isoxazol-5-yl][(6-(4-pyridylthio)(3-pyridyl))amino]carboxamide ' 247 {[3-(tart-butyl)isoxazol-5-yl]amino}-N-{3-[2-(N-methylcarbamoyl)(4-pyridyloxy)]phenyl} carboxamide 253 N-[3-(1,1-dimethylpropyl)isoxazol-5-yl][(3-(4-pyridylthio)phenyl)amino]carboxamide ' 255 N-[3-(1,1-dimethylpropyl)isoxazol-5-yl][(4-(4-pyridyloxy)phenyl)amino] carboxamide 261 N-[3-(1,1-dimethylpropyl)isoxazol-5-yl]({4-[2-(N-methylcarbamoyl)(4-pyridyloxy)]phenyl} axnino)carboxamide 263 N-[3-(1,1-dimethylpropyl)isoxazol-5-yI]{[4-(2-methyl(4-pyridylthio))phenyl]amino} carboxamide 292 N-[3-(tent-butyl)pyrazol-5-yl] {[4-(6-methyl(3-pyridyloxy))phenyl]amino} carboxamide 29~ ~[3-(tent-butyl)pyrazol-5-yl]amino}-N-(3-(4-pyridylthio)phenyl)carboxamide 299 N-[3-(tent-butyl)pyrazol-5-yl][(4-(4-pyridylthio)phenyl)amino]carboxamide 300 ~3-[4-({[3-(tent-butyl)pyrazol-5-yl]amino} carbonylarriino)phenoxy]phenyl}-N-methylcarboxamide, 2,2,2-trifluoroacetic acid 304 N-[3-(tert-butyl)-1-rilethylpyrazol-5-yl]
{[4-(4-pyridylmethoxy)phenyl] amino} carboxamide 305 {5-[4-({[3-(tert-butyl)-1-methylpyrazol-5-yl] amino } carbonylamino)phenoxy]-2-methoxyphenyl } -N-methylcarboxamide 309 N-[3-(tent-butyl)-1-methylpyrazol-5-yl][(3-(4-pyridylthio)phenyl)amino]carboxamide 321 N-[3-(tent-butyl)-1-methylpyrazol-5-yl][(4-(4-pyridyloxy)phenyl)amino]carboxamide 326 N-[3-(tent-butyl)-1-methylpyrazol-5-yl] ~[4-(4-pyridylmethyl)phenyl]amino} carboxamide 339 tert-butyl 3-(tent-butyl)-5-[({4-[3-(N-methylcarbamoyl)phenoxy]phenyl} amino)carbonylamino]pyraz olecarboxylate 341 N-[5-(tent-butyl)(1,3,4-thiadiazol-2-yl)][(4-(4-pyridyloxy)phenyl)amino]carboxamide 342 {[5-(tent-butyl)(1,3,4-thiadiazol-2-yl)]amino}-N-(3-(4-pyridylthio)phenyl)carboxamide 356 N-[5-(tent-butyl)(1,3,4-thiadiazol-2-yl)]
~[6-(6-methyl(3-pyridyloxy))(3-pyridyl)] amino } carboxamide 366 N-[5-(1,1-dirnethylpropyl)(1,3,4-thiadiazol-2-yl)][(4-{4-pyridyloxy)phenyl)amino]carboxamide 367 N-[5-(1,1-dimethylpropyl)(1,3,4-thiadiazol-2-yl)][(3-(4-pyridylthio)phenyl)amino]carboxamide 376 N-[5-(tert-butyl)(3-thienyl)][(4-(3-pyridyloxy)phenyl)amino]carboxamide 388 {3-[4-({[5-(tert-butyl)(1,3,4-oxadiazol-2-yl)] amino } carbonylamino)phenoxy]phenyl } -N-ethylcarboxamide 389 ~3-[4-({[5-(tert-butyl)(1,3,4-oxadiazol-2-yl)] amino } c arbonylamino)phenoxy]phenyl } -N-(methylethyl)carboxamide 390 ~3-[4-(~[5-(tent-butyl)(1,3,4-oxadiazol-2-yl)]amino} carbonylamino)phenoxy]phenyl}-N-methylcarboxamide 391 N-[5-(tert-butyl)(1,3,4-oxadiaz~ol-2-yl)][(4-(4-pyridyloxy)phenyl)amino]carboxamide 392 N-(3-cyclopropyl-1-methylpyrazol-5-yl)[(4-(6-quinolyloxy)phenyl)amino] carboxamide 393 (~4-[2-(N-methylcarbamoyl)(4-pyridyloxy)]phenyl}amino)-N-(1-methyl-3-phenylpyrazol-S-yl)carboxamide 395 N-[2-(tent-butyl)(1,3-fhiazol-5-yl)] ~[4-(6-methyl(3-pyridyloxy))phenyl]amino}carboxamide From WO 1999132110 Entry Name No 1 [(2,3-dichlorophenyl)amino]-N-[3-(tert-butyl)-1-phenylpyrazol-5-yl]carboxamide ' 2 N-[1-(4-aminophenyl)-3-(tert-butyl)pyrazol-5-yl][(2,3-dichlorophenyl)amino]carboxamide 11 N-[1-(3-aminophenyl)-3-(tert-butyl)pyrazol-5-yl][(2,3-dichlorophenyl)amino]carboxamide 18 N-[3-(3-(tent-butyl)-5-{[(4-phenoxyphenyl) amino]carbonylamino}pyrazolyl)phenyl]acetamide 23 N-[1-(2,6-dichlorophenyl)-3-(tent-butyl)pyrazol-5-yl]
~[4-(4-pyridylmethyl)phenyl] amino } carboxamide 24 N-[3-(tert-butyl)-1-(~.-fluorophenyl)pyrazol-5-yl]
{[4-(4-pyridylmethyl)phenyl] amino} carboxamide 25 N-[3-(tent-butyl)-1-(2-methylphenyl)pyrazol-5-yl]
f [4-(4-pyridylmethyl)phenyl] amino} carboxamide 26 ~ N-[3-(tert-butyl)-1-(3-fluorophenyl)pyrazol-5-yl]
f [4-(4-pyridylmethyl)phenyl] amino} carboxamide 27 N- f 3-(tert-butyl)-1-[4-(methylsulfonyl)phenyl]pyrazol-5-yl} {[4-(4-pyridylmethyl)phenyl]amino}carboxamide 28 N-[3-(tert-butyl)-1-(4-nitrophenyl)pyrazol-5-yl]
{[4-(4- .

pyridylmethyl)phenyl] amino} carboxamide 29 N-[3-(tert-butyl)-1-(3-methoxyphenyl)pyrazol-5-yl]
{[4-(4-, pyridylmethyl)phenyl] amino} carboxamide 30 N-[1-(3-amirlophenyl)-3-(tert-butyl)pyrazol-5-yl]
~[4-(4-pyridylmethyl)phenyl]amino } carboxamide 32 N-[1-(3-aminophenyl)-3-(tert-butyl)pyrazol-5-yl][(4-(4-pyridylthio)phenyl)amino]carboxamide 34 N-[3-(tert-butyl)-1-(3-fluorophenyl)pyrazol-5-yl][(3-(4-pyridylthio)phenyl)amino]carboxamide 35 N-[3-(tert-butyl)-1-(4-fluorophenyl)pyrazol-5-yl][(3-(4-pyridylthio)phenyl)amino] carboxamide 36 N-[3-(tent-butyl)-1-(3-fluorophenyl)pyrazol.-5-yl][(4-(4-pyridyloxy)phenyl)amino]carboxamide 37 N-[3-(tert-butyl)-1-(4-fluorophenyl)pyrazol-5-yl][(4-(4-pyridyloxy)phenyl)amino]carboxamide From WO 1999/32455 Entry Name No 1 [(2,3-dichlorophenyl)amino]-N-[3-(tert-butyl)-1-phenylpyrazol-5-yl]carboxamide 2 N-[1-(4-aminophenyl)-3-(tent-butyl)pyrazol-5-yl][(2,3-dichlorophenyl)amino]carboxamide 14 N-[1-(3-aminophenyl)-3-{tei-t-butyl)pyrazol-S-yl][(2,3-dichlorophenyl)amino]carboxamide 22 N-[3-(3-(tert-butyl)-5-{[(4-phenoxyphenyl) amino] carbonylamino } pyrazolyl)phenyl]
ac etamide 27 N-[1-(2,6-dichlorophenyl)-3-(tert-butyl)pyrazol-5-yl]
f [4-(4-pyridylmethyl)phenyl] amino} carboxamide 28 N-[3-(tert-butyl)-1-(4-fluorophenyl)pyrazol-5-yl]
f [4-(4-pyridylmethyl)phenyl]amino}carboxamide 29 N-[3-(tent-butyl)-1-(2-methylphenyl)pyrazol-S-yl]
f [4-(4-pyridylmethyl)phenyl] amino } carboxamide 30 N-[3-(tert-butyl)-1-(3-fluorophenyl)pyrazol-5-yl]
{[4-(4-pyridylinethyl)phenyl]amino} carboxamide 31 N- f 3-(tert-butyl)-1-[4-(methylsulfonyl)phenyl]pyrazol-5-yl} {[4-(4-pyridylmethyl)phenyl]amino}carboxamide 32 N-[3-(tert-butyl)-l.-(4-nitrophenyl)pyrazol-5-yl]
{[4-(4-pyridylinethyl)phenyl]amino} carboxamide 33 N-[3-(tert-butyl)-1-(3-methoxyphenyl)pyrazol-5-yl]
{[4-(4-.

pyridylmethyl)phenyl] amino} carboxamide 34 N-[I-(3-aminophenyl)-3-(tert-butyl)pyrazol-5-yl]~[4-(4-pyridylmethyl)phenyl] amino} carboxamide 36 N-[1-(3-aminophenyl)-3-(tert-butyl)pyrazol-5-yl][(4-(4-pyridylthio)phenyl)amino]carboxamide From ~O 2000/41698 Entr Name No 1 {3-[4-({[3-(tert-butyl)phenyl] amino} carbonylarnino)phenoxy]phenyl}
-N-methylcarboxamide 11 N-[2-methoxy-5-(trifluoromethyl)phenyl]({3-[2-(N-methylcarbamoyl)(4- yridyloxy)] henyl}amino)carboxamide 12 4-[3-( {N-[2-methoxy-5-(trifluoromethyl)phenyl] carbanioyl} amino)phenoxy]pyridine-2-carboxamide
13 N-[2-methoxy-5-(trifluoromethyl)phenyl]({4-[2-(N-methylcarbamoyl)(4- yridyloxy)] henyl amino)carboxamide
14 4-[4-( {N-[2-methoxy-5-(trifluoromethyl)phenyl]carbamoyl} amino)phenoxy]pyridine-2-carboxamide 16 {4-[4-( {N-[2-methoxy-5-(trifluoromethyl)phenyl] carbamoyl} amino)-3-methyl henoxy (2-pyridyl)}-N-methylcarboxamide 17 ( {2-chloro-4-[2-(N-methylcarbamoyl)(4-pyridyloxy)]phenyl} amino)-N-[2-methoxy-5-(trifluoromethyl) henyl]carboxatizide 19 ( {4-[2-(N-ethylcarbamoyl)(4-pyridyloxy)]phenyl's amino)-N-[2-methoxy-5-(trifluoroinethyl) henyl]carboxamide 20 ( {3-chloro-4-[2-(N-methylcarbamoyl)(4-pyridyloxy)]phenyl} amino)-N-[2-methoxy-5--(trifluoromethyl) h'enyl carboxamide .

22 3-[4-({N-[2-methoxy-5- -(trifluoromethyl) henyl]carbamoyl}amino) henoxy]benzamide 24 ( {4-[2-(N,N-dimethylcarbamoyl)(4-pyridyloxy)]phenyl}
amino)-N-[2-methoxy-5-(trifluoromethyl) henyl]carboxamide 27 N-[2-methoxy-5-(trifluoromethyl)phenyl]({4-[2-{N-methylcarbamoyl)(4- yridylthio) henyl} amino)carboxamide 29 N-[2-methoxy-5-(trifluoromethyl)phenyl]({3-[2-(N-methylcarbamoyl)(4- yridylthio)] henyl} amino)carboxamide 31 N-[2-methoxy-5-(trifluoromethyl)phenyl][(4-{5-[N-{2-morpholin-4-ylethyl)carbamoyl] (3-yridyloxy)} henyl)amino]caxboxamide 32 ~ N-[2-methoxy-5-(trifluoromethyl)phenyl]({4-[5-(N-methylcarbamoyl)(3-pyridyloxy) henyl}amino)carboxamide 34 N-[2-rnethoxy-5-(trifluoromethyl)phenyl]({4-[3-(N-(3-yridyl)carbamoyl) henoxy] henyl amino)carboxamide 42 {4-[4-({[4-chloro-3-(trifluoromethyl)phenyl] amino} carbonylamino)phenoxy]
(2-yridyl) -N-rnethylcarboxamide 43 4-[4-({[4-chloro-3-(trifluoromethyl)phenyl] amino} carbonylamino)phenoxy]pyridin - e-2-carboxamide 44 4-[3-({[4-chloro-3-(trifluoromethyl)phenyl] amino} carbonylamino)phenoxy]pyridin e-2-carboxamide 45 {[4-chloro-3-(trifluoromethyl)phenyl]amino}-N-{3-[2-(N-methylcarbamoyl) 4- yridyloxy) henyl} carboxamide 47 {[4-chloro-3-(trifluoromethyl)phenyl]amino}-N-{2-methyl-4-[2-(N-methylcarbamoyl)(4- yridyloxy)] henyl}carboxamide 49 {4-[3-chloro-4-({[4-chloro-3-(trifluoromethyl)phenyl] amino } carbonylamino)phenoxy]
(2-yridyl)}-N-methylcarboxamide 51 N-[4-chloro-3-(trifluoromethyl)phenyl]( {4-[2-(N-ethylcarbamoyl) 4-pyridyloxy)] henyl}amino)carboxamide 61 {3-[4-({[4-chloro-3-(trifluoromethyl)phenyl]amino} carbonylamino)phenoxy]phenyl }-N-(2-mo holin-4-ylethyl)carboxamide 62 {3-[4-({[4-chloro-3-(trifluoromethyl)phenyl] amino } carbonylamino)phenoxy]phenyl -N- 2- i eridylethyl)carboxamide 65 {4-[4-({[4-chloro-3-(trifluoromethyl)phenyl] amino } carbonylamino)phenylthio]
(2-yridyl)}-N-methylcarboxamide 69 {[4-chloro-3-(trifluoromethyl)phenyl]amino}-N-{3-[2-(N-.

methylcarbarnoyl)(4- yridylthio)] henyl} carboxamide 70 {4-[4-({[4-chloro-3-(trifluoromethyl)phenyl] amino } carbonylamino)phenoxy],(2-yridyl)}-N- 2-mo holin-4-ylethyl)carboxamide 72 {5-[4-({[4-chloro-3-(trifluoromethyl)phenyl amino}carbonylamino)phenoxy](3-yridyl) } -N-methylcarboxamide 75 N-[4-chloro-3-(trifluoromethyl)phenyl]({4-[3-(N-(3-yridyl)carbamoyl) henoxy] henyl} amino)carboxamide 84 {4-[4-({[4-chloro-3-(trifluoromethyl)phenyl]amino} carbonylamino)phenoxy](2-yridyl)}-N-(2-hydroxyethyl)carboxarnide 87 {4-[4-({[4-bromo-3-(trifluoromethyl)phenyl]amino} carbonylamino)-2-chloro henox (2- yridyl) -N-methylcarboxamide 88 N-[4-bromo-3-(trifluoromethyl)phenyl]({4-[2-(N-ethylcarbamoyl).4- yridyloxy) henyl}amino)carboxamide 89 {[4-bromo-3-(trifluoromethyl)phenyl]amino}-N-{3-[2-(N-methylcarbamoyl)(4- yridyloxy)] henyl}carboxamide 90 {[4-bromo-3-(trifluoromethyl)phenyl]amino}-N-{4-methyl-3-2-(N-methylcarbamoyl) 4- yridyloxy)] henyl}carboxamide 93 {[4-bromo-3-(trifluoromethyl)phenyl]amino}-N-{3-[2-(N-methylcarbamoyl)(4- yridylthio)] henyl} carboxamide 94 {4-[4-({[4-bromo-3-(trifluoromethyl)phenyl] amino } carb onylamino)phenoxy]
(2-yridyl)}-N-(2-morpholin-4-ylethyl)carboxamide 95 N-[4-chloro-2-methoxy-5-(trifluoromethyl)phenyl]
( {4-[2-(N-methylcarbamoyl)(4- yridyloxy)] henyl}amino)carboxamide 96 N-[4-chloro-2-methoxy-5-(trifluoromethyl)phenyl]({2-chloro-4-[2-(N-methylcarbamoyl)(4-yridyloxy)] henyl} amino)carboxamide_ 97 N-[4-chloro-2-methoxy-5-(trifluoromethyl)phenyl]({3-chloro-4-[2-(N-methylcarbamoyl)(4-yridyloxy)] henyl} amino)carboxamide 98 N-[4-chloro-2-methoxy-5-(trifluoromethyl)phenyl]({3-[2-(N-meth lcarbamoyl)(4- ~ridyloxy)] henyl} amino)carboxamide 99 N-[4-chloro-2-methoxy-5-(trifluoromethyl)phenyl]({4-[2-(N-ethylcarbamoyl) 4- yridyloxy)] henyl amino)carboxamide From WO 2000/42012 Ent No Name 1. {3-[4-({[3-(tent-butyl)phenyl]amino} carbonylamino)phenoxy]phenyl}-N-methylcarboxamide 11 N-[2-methoxy-5-(trifluoromethyl)phenyl]({3-[2-(N-rnethylcarbamoyl)(4- yridyloxy)] henyl} amino)carboxamide 12 4-[3-( ~N-[2-methoxy-5-(trifluoromethyl)phenyl]carbamoyl} amino)phenoxy]pyridine-2-carboxamide 13 N-[2-methoxy-5-(trifluoromethyl)phenyl]( f 4-[2-(N-methylcarbamoyl)(4- yridyloxy) henyl amino)carboxamide 14 4-[4-(~N-[2-methoxy-5- .

(trifluoromethyl)phenyl]carbamoyl} amino)phenoxy]pyridine-2-carboxamide 16 (4-[4-( {N-[2-methoxy-5- .

(trifluoromethyl)phenyl]carbamoyl} amino)-3-.

methyl henox ](2- yridyl)}-N-methylcarboxamide 17 (~2-chloro-4-[2-(N-methylcarbamoyl)(4-pyridyloxy)]phenyl} amino)-N-[2-methoxy-5-(trifluoromethyl) henyl carboxamide 19 ( {4-[2-(N-ethylcarbamoyl)(4-pyridyloxy)]phenyl}
amino)-N-[2-methoxy-5-(trifluoromethyl) henyl carboxamide 20 ({3-chloro-4-[2-(N-methylcarbamoyl)(4-pyridyloxy)]phenyl} amino)-N-[2-methoxy-5-(trifluoromethyl) henyl]carboxamide 22 3-[4-(~N-[2-methoxy-5-(trifluoromethyl) henyl carbamoyl}amino) henoxy benzamide 24 ({4-[2-(N,N-dimethylcarbamoyl)(4-pyridyloxy)]phenyl}arnino)-N-[2-methoXy-5-(trifluoromethyl) henyl]carboxamide 27 N-[2-methoxy-5-(trifluoromethyl)phenyl](~4-[2-(N-methylcarbamoyl)(4- yridylthio)] hen 1} amino)carboxamide 29 N-[2-methoxy-5-(trifluoromethyl)phenyl]( f 3-[2-(N-methylcarbamoyl)(4- yridylthio)] henyl} amino)carboxamide 31 N-[2-methoxy-5-(trifluoromethyl)phenyl][(4-{5-[N-(2-morpholin-4-ylethyl)carbamoyl] (3-yridyloxy)} henyl)amino]carboxamide 32 N-[2-methoxy-5-(trifluoromethyl)phenyl]({4-[5-(N-methylcarbamoyl)(3- yridyloxy) henyl} amino)carboxamide 34 N-[2-methoxy-5-{trifluoromethyl)phenyl]( f 4- 3-(N-(3-pyridyl)carbamoyl) henoxy phenyl} amino)carboxamide 42 {4-[4-({[4-chloro-3-(trifluoromethyl)phenyl] amino } c arbonylamino)phenoxy]
(2-yridyl) } -N-methylcarboxamide 43 4-[4-({[4-chloro-3-(trifluoromethyl)phenyl] amino} carbonylamino)phenoxy]pyridin e-2-carbo'xamide 44 4-[3-({[4-chloro-3-(trifluoromethyl)phenyl] amino} carbonylamino)phenoxy]pyridin e-2-carboxamide 45 ~[4-chloro-3-(trifluoromethyl)phenyl]amino}-N-{3-[2-(N-methylcarbamoyl)(4- yridyloxy)] henyl}carboxamide 47 ~[4-chloro-3-(trifluoromethyl)phenyl]amino}-N-~2-methyl-4-[2- -methylcarbamoyl)(4- yridyloxy)] henyl}carboxamide 49 ~4-[3-chloro-4-(f[4-chloro-3-(trifluoromethyl)phenyl] amino } c arbonylamino)phenoxy]
(2-pyridyl)}-N-methylcarboxamide 51. N-[4-chloro-3-(trifluoromethyl)phenyl](~4-[2-(N-ethylcarbamoyl)(4- yridyloxy)] henyl amino)carboxamide 61 ~3-[4-(~[4-chloro-3- -(trifluoromethyl)phenyl] amino } carbonylamino)phenoxy]phenyl }-N- 2-mo holin-4-ylethyl)carboxamide 62 ~3-[4-({[4-chloro-3-(trifluoromethyl)phenyl]amino}carbonylamino)phenoxy]phenyl -}-N-(2- i eridylethyl)carboxamide 65 f4-[4-(~[4-chloro-3-(trifluoromethyl)phenyl] amino } carbonylamino)phenylthio]
(2-yridyl) -N-methylcarboxamide 69 ~[4-chloro-3-(trifluoromethyl)phenyl]amino}-N-{3-[2-(N-methylcarbamoyl)(4- yridylthio)] henyl carboxamide 70 f 4-[4-( f [4-chloro-3-(trifluoromethyl)phenyl]amino}carbonylarnino)phenoxy](2-.

yridyl)}-N-(2-mo holin-4-ylethyl)carboxamide 72 ~5-[4-(~[4-chloro-3-(trifluoromethyl)phenyl]amino}carbonylamino)phenoxy](3-, yridyl)}-N-methylcarboxamide 75 N-[4-chloro-3-(trifluoromethyl)phenyl]( 4-[3-(N-(3-yridyl)carbamoyl) henoxy] henyl} amino)carboxamide 84 {4-[4-({[4-chloro-3-(trifluoromethyl)phenyl] amino } carbonylamino)phenoxy]
(2-yridyl) } -N-(2-hydroxyethyl)carboxamide 87 {4-[4-({[4-bromo-3-(trifluoromethyl)phenyl] amino} carbonylarnino)-2-chlorophenoxy (2- yridyl)}-N-methylcarboxamide 88 N-[4-bromo-3-(trifluoromethyl)phenyl]({4-[2-(N-ethylcarbamoyl (4-pyridyloxy)] henyl} amirio)carboxamide 89 {[4-bromo-3-(trifluoromethyl)phenyl]amino}-N-{3-[2-(N-methylcarbamoyl)(4- yridyloxy) henyl}carboxamide 90 {[4-bromo-3-(trifluoromethyl)phenyl]amino}-N-{4-methyl-3-[2-(N-methylcarbamoyl) 4- yridyloxy)] henyl}
carboxamide 93 {[4-bromo-3-(trifluoromethyl)phenyl]amino}-N-{3-[2-(N-methylcarbamoyl)(4- yridylthio)] henyl}carboxamide 94 {4-[4-({[4-bromo-3-(trifluoromethyl)phenyl] amino } carbonylamino)phenoxy]
(2-yridyl) -N-(2-mo holin-4-ylethyl)carboxamide 95 N-[4-chloro-2-methoxy-5-(trifluoromethyl)phenyl]({4-[2-{N-methylcarbamoyl)(4- yridyloxy) henyl}amino)carboxamide 96 N-[4-chloro-2-methoxy-5-(trifluoromethyl)phenyl]({2-chloro-4-[2-(N-methylcarbamoyl)(4-yridyloxy)] henyl} arnino)carboxamide 97 N-[4-chloro-2-methoxy-5-(trifluoromethyl)phenyl]({3-chloro-4-[2-(N-methylcarbamoyl)(4-yridyloxy)] henyl} amino)carboxamide 98 N-[4-chloro-2-methoxy-5-(trifluoromethyl)phenyl]({3-[2-(N-methylcarbamo 1 (4- yridyloxy)] henyl} amino)carboxamide 99 N-[4-chloro-2-methoxy-5-(trifluoromethyl)phenyl]({4-[2-(N-ethylcarbamoyl)(4- yridyloxy)] henyl} amino)carboxamide From WO 2002/85859 Entry Name No 16 [(4-fluorophenyl)amino]-N-(3-isoquinolyl)carboxamide 25 N-(2-methoxy(3-quinolyl))[(4-(4-pyridyloxy)phenyl)amino] caxboxamide 27 N-(2-methoxy(3-quinolyl))[(3-(4-pyridylthio)phenyl)amino]carboxamide 28 N-[1-(4-methylpiperazinyl)(3-isoquinolyl)][(4-(4-pyridyloxy)phenyl)amino]carboxamide From WO 2002/85857 Entry Name No 2~ N-(2-methoxy(3-quinolyl))[(4-(4-pyridyloxy)phenyl)amino]carboxamide 27 N-(2-methoxy(3-quinolyl))[(3-(4-pyridylthio)phenyl)amino] carboxamide 28 N-[1-(4-methylpiperazinyl)(3-isoquinolyl)][(4-(4-pyridyloxy)phenyl)amino]carboxamide Cell mechanistic assay-Inhibition of 3T3 KDR phosphorylation: .
NIH3T3 cells expressing the full length KDR receptor are grown in DMEM
(Life Technologies, Inc., Grand Island, NY) supplemented with 10% newborn calf serum, low glucose, 25 mM/L sodium pyruvate, pyridoxine hydrochloride and 0.2 mg/ml of 6418 (Life Technologies Inc., Grand Island, NY). The cells are maintained in collagen I-coated T75 flasks (Becton Dickinson Labware, Bedford, MA) in a humidified 5% C02 atmosphere at 37°C.
Fifteen thousand cells are plated into each well of a collagen I-coated 96-well plate in the DMEM growth medium. Six hours later, the cells are washed and the medium is replaced with DMEM without serum. After overnight culture to quiesce the cells,t he medium is replaced by Dulbecco's phosphate-buffered saline (Life Technologies Inc., Grand Island, NY) .with 0.1% bovine albumin (Sigma Chemical Co., St. Louis, MO). After adding various concentrations (0-300 nM) of test compounds to the cells 'in 1% final concentration of DMSO, the cells are incubated at room temperature for 30 minutes. Following VEGF stimulation, the . buffer is removed and the cells are lysed by addtion of 150 wl of extraction buffer (50 mlVl Tris, pH 7.8, supplemented with 10% glycerol, 50 mM BGP, 2 mM EDTA, 10 mM NaF, 0.5 mM NaV04, and 0.3% TX-100) at 4°C for 30 minutes.
5 To assess receptor pliosphorylation, 100 microliters of each cell lysate are added to the wells of an ELISA plate precoated with 300 ng of antibody C20 (Santa Cruz Biotechnology, Inc., Santa Cruz, CA). Following a 60-minute incubation, the plate is washed and bound KDR is probed for phosphotyrosine using an anti-phosphotyrosine mAb clone 4610 (Upstate Biotechnology, Lake Placid, NY). The 10 plate is washed and wells are incubated with anti-mouse IgG/HRP conjugate (Amersham International plc, Buckinghamshire, England) for 60 minutes. Wells are washed and phosphotyrosine is quantitated by addition of 100 ~,1 per well of 3,3',5,5' tetrarnethylbenzidine (I~irkegaard and Ferry, TMB 1 Component Stop Solution).
15 Optical densities (OD) are determined spectrophotometrically at 450 mm in a 96-well plate reader (SpectraMax,250, Molecular Devices). Background (no VEGF
added) OD values are subtracted from all Ods and .percent inhibition is calculated according to the equation:
20 % Inhibition = ~OD(VEGF controls - OD(with test compound)' 100 OD(VEGF control) - OD(no VEGF added) ICsos are determined on some of the exemplary materials with at least squares analysis program using compound concentration versus percent~inhibition.
Matrig_el~o~enesis Model:
Preparation of Martigel Plugs and in vivo Phase: Matrigel~ (Collaborative Biomedical Products, Bedord, MA) is a basement membrane extract from a murine tumor composed primarily of laminin, collagen IV and heparan sulfate proteoglycan.
It is provided as a sterile liquid at 4°C, but rapidly forms a solid gel at 37°C.

Liquid Matrigel at 4°C is mixed with SK-MEL2 human tumor cells that are transfected with a plasmid containing the marine VEGF gene with a selectable marker. Tumor cells are grown in ~it~o under selection and cells are mixed with cold liquid Matrigel at a ratio of 2 X 106 per 0.5 ml. . One half milliliter is implanted subcutaneously near the abdominal midline using a 25 gauge needle. Test compounds are dosed as solutions in Ethanol/Ceremaphor EL/saline (12.5%:12.5%:75%) at 30, 100, and 300 mg/kg .po once daily starting on the day of implantation. Mice are euthanized 12 days post-implantation and the Matrigel pellets are harvested for analysis of hemoglobin content.
Hemoglobin Assay: The Matrigel pellets are placed in 4 volumes (w/v) of 4°C
Lysis Buffer (20mM Tris pH 7.5, 1mM EGTA, 1mM EDTA, 1% Triton X-100 [EM
Science, Gibbstown, N.J.], and complete EDTA-free protease inhibitor cocktail [Mannheim, Germany]), and homogenized at 4°C. homogenates are incubated on ice for 30 minutes with shaking and centrifuged at 14.K x g for 30 minutes at 4°C.
Supernatants are transferred to chilled microfuge tubes and stored at 4°C for hemoglobin assay:
Mouse hemoglobin (Sigma Chemical Co., St. Louis, MO) is suspended in autoclaved water .(BioWhittaker, Inc, Walkersville, MD.) at 5 mg/ml. ~ A
standard curve is generated from 500 micrograms/ml to 30 micrograms/rnl in Lysis Buffer (see above). Standard curve and lysate samples are added at 5 microliters/well in duplicate to a polystyrene 96-well plate. Using the Sigma Plasma Hemoglobin Kit (Sigma Chemical Co., St. Louis, MO), TMB substrate is reconstituted in 50 mls room temperature acetic acid solution. One hundred microliters of substrate is added to each well, folloyved by 100 microliters/well of Hydrogen Peroxide Solution at room temperature. The plate is incubated at room temperature for 10 minutes.
Optical densities are determined spectrophotometrically at 600 nm in a 96-well plate reader, SpectraMax 250 Microplate Spectrophotometer System (Molecular Devices, Sunnyvale, CA). Background Lysis Buffer readings are subtracted from all wells.

Total sample hemoglobin content is calculated according to the following equation:
Total Hemoglobin = (Sample Lysate Volume) x (Hemoglobin Concentration) The average Total Hemoglobin of Matrigel samples without cells is subtracted from each Total Hemoglobin Matrigel sample with cells. Percent inhibition is calculated according to the following equation:
Inhibition = ~Avera~e Total Hemoglobin Drug-Treated. Tumor Lysates) X 100 (Average Total Hemoglobin Non-Treated Tumore Lysates).
The preceding examples can be repeated with similar success by substituting the generically or specifically described reactants and/or operating conditions of this, invention for those used in the preceding examples.
From the foregoing description, 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 conditions and usages.

Claims (36)

1. A method for treating or preventing a disease in a human or other mammal regulated by tyrosine kinase (associated with an aberration in the tyrosine kinase signal transduction pathway), comprising administering to a human or other mammal in need thereof a compound of Formula I, a salt form of a compound of Formula I, an isomer of a compound of Formula I or a prodrug of a compound of Formula I

A-NH-C(O)-NH-B I

wherein A is selected from the group consisting of (i) phenyl, optionally substituted with 1-3 substituents independently selected from the group consisting of R1, OR1, NR1R2, S(O)q R1, SO2NR1R2, NR1SO2R2, C(O)R1, C(O)OR1, C(O)NR1R2, NR1C(O)R2, NR1C(O)OR2, halogen, cyano, and nitro;
(ii) naphthyl, optionally substituted with 1-3 substituents independently selected from the group consisting of R1, OR1, NR1R2, S(O)q R1, SO2NR1R2, NR1SO2R2, C(O)R1, C(O)OR1, C(O)NR1R2, NR1C(O)R2; NR1C(O)OR2, halogen, cyano, and nitro;
(iii) 5 and 6 membered monocyclic heteroaryl groups, having 1-3 heteroatoms independently selected from the group consisting of O, N and S, optionally substituted with 1-3 substituents independently selected from the group consisting of R1, OR1, NR1R2, S(O)q R1, SO2NR1R2, NR1SO2R2, C(O)R1, C(O)OR1, C(O)NR1R2, NR1C(O)R2, NR1C(O)OR2, halogen, cyano, and nitro; and (iv) 8 to 10 membered bicyclic heteroaryl group in which the first ring is bonded to the NH of Figure I and contains 1-3 heteroatoms independently selected from the group consisting of O, N, and S, and the second ring is fused to the first ring using 3 to 4 carbon atoms, the bicyclic heteroaryl group is optionally substituted with 1-3 substituents independently selected from the group consisting of R1, OR1, NR1R2, S(O)q R1, SO2NR1R2, NR1SO2R2, C(O)R1, C(O)OR1, C(O)N1R1R2, NR1C(O)R2, NR1C(O)OR2, halogen, cyano, and nitro, B is selected from the group consisting of (i) phenyl, optionally substituted with 1-3 substituents independently selected from the group consisting of-L-M, C1-C5 linear or branched alkyl, C1-C5 linear or branched haloalkyl, C1-C3 alkoxy, hydroxy, amino, C1-C3 alkylamino, C1-C6 dialkylamino, halogen, cyano, and nitro;
(ii) naphthyl, optionally substituted with 1-3 substituents independently selected from the group consisting of-L-M, C1-C5 linear or branched alkyl, C1-C5 linear or branched haloalkyl, C1-C3 alkoxy, hydroxy, amino, C1-C5 alkylamino, C1-C6 dialkylamino, halogen, cyano, and nitro;
(iii) 5 and 6 membered monocyclic heteroaryl groups, having 1-3 heteroatoms independently selected from the group consisting of O, N and S, optionally substituted with 1-3 substituents independently selected from the group consisting of-L-M, C1-C5 linear or branched alkyl, C1-C5 linear or branched haloalkyl, C1-C3 alkoxy, hydroxy, amino, C1-C3 alkylamino, C1-C6 dialkylamino, halogen, cyano, and nitro; and (iv) 8 to 10 membered bicyclic heteroaryl groups having 1-6 heteroatoms independently selected from the group consisting of O, N and S, optionally substituted with 1-3 substituents independently selected from the group consisting of-L-M, C1-C5 linear or branched alkyl, C1-C5 linear or branched haloalkyl, C1-C3 alkoxy, hydroxy, amino, C1-C3 alkylamino, dialkylamino, halogen, cyano, and nitro.

L is selected from the group consisting of:
(a) -(CH2)m-O-(CH2)l-(b) -(CH2)m-(CH2)l-, (c) -(CH2)m-C(O)-(CH2)l, (d) -(CH2)m-NR3-(CH2)l,-(e) -(CH2)m- NR3C(O)-(CH2)l-, (f) -(CH2)m-S-(CH2)l, (g) (CH2)m-C(O)NR3 -(CH2)l-, (h) -(CH2)m-CF2-(CH2)l-, (i) -(CH2)m-CCl2-(CH2)l-, (j) -(CH2)m-CHF-(CH2)l-, (k) -(CH2)m-CH(OH)-(CH2)l-, (l) -(CH2)m-C~-(CH2)l-(m) -(CH2)m-C=C-(CH2)l, and (n) a single band, where m and 1 are 0;
(a) -(CH2)m-CR4R5-(CH2)l-;
wherein the variables m and 1 are integers independently selected from 0-4, M is selected from the group consisting of:
(i) phenyl, optionally substituted with 1-3 substituents independently selected from the group consisting of R1, OR1, NR1R2, S(O)q R1, SO2NR1R2, NR1SO2R2, C(O)R1, C(O)OR1, C(O)NR1R2, NR1C(O)R2, NR1C(O)OR2, halogen, cyano and nitro;
(ii) naphthyl, optionally substituted with 1-3 substituents independently selected from the group consisting of R1, OR1, NR1R2, S(O)q R1, SO2NR1R2, NR1SO2R2, C(O)R1, C(O)OR1, C(O)NR1R2; NR1C(O)R2, NR1C(O)OR2, halogen, cyano and nitro;
(iii) 5 and 6 membered monocyclic heteroaryl groups, having 1-3 heteroatoms independently selected from the group consisting of O, N and S, optionally substituted with 1-3 substituents independently selected from the group consisting of R1, OR1, NR1R2, S(O)q R1, SO2NR1R2, NR1SO2R2, C(O)R1, C(O)OR1, C(O)NR1R2, NR1C(O)R2, NR1C(O)OR2, halogen, cyano and nitro and also oxides (e.g. =O, -O~ or -OH); and (iv) 8 to 10 membered bicyclic heteroaryl groups, having 1-6 heteroatoms independently selected from the group consisting of O, N and S, optionally substituted with 1-3 substituents independently selected from the group consisting of R1, OR1, NR1R2, S(O)q R1, SO2NR1R2, NR1SO2R2, C(O)R1, C(O)OR1, C(O)NR1R2, NR1C(O)R2, NR1C(O)OR2, halogen, cyano and nitro and also oxides (e.g. =O, -O~ or -OH).

(v) saturated and partially saturated C3-C6 monocyclic carbocyclic moiety optionally substituted with 1-3 substituents independently selected from the group consisting of R1, OR1, NR1R2, S(O)q R1, SO2NR1R2, NR1SO2R2, C(O)R1, C(O)OR1, C(O)NR1R2, NR1C(O)R2, NR1C(O)OR2, halogen, cyano and, nitro;

(vi) saturated and partially saturated C8-C10 bicyclic carbocyclic moiety, optionally substituted with 1-3 substituents independently selected from the group consisting of R1, OR1, NR1R2, S(O)q R1, SO2NR1R2, NR1SO2R1, C(O)R1, C(O)OR1, C(O)NR1R2, NR1C(O)R2, NR1C(O)OR2, halogen, cyano and nitro;
(vii) saturated and partially saturated 5 and 6 membered monocyclic heterocyclic moiety, having 1-3 heteroatoms independently selected from the group consisting of O, N and S, optionally substituted with 1-3 substituents independently selected from the group consisting of R1, OR1, NR1R2, S(O)q R1, SO2NR1R2, NR1SO2R2, C(O)R1, C(O)OR1, C(O)NR1R2, NR1C(O)R2, NR1C(O)OR2, halogen, cyano and nitro, and also oxides (e.g. =O, -O~ or -OH);
and (viii) saturated and partially saturated 8 to 10 membered bicyclic heterocyclic moiety, having 1-6 heteroatoms independently selected from the group consisting of O, N and S, optionally substituted with 1-3 substituents independently selected from the group consisting of R1, OR1, NR1R2, S(O)q R1, SO2NR1R2, NR1SO2R2, C(O)R1, C(O)OR1, C(O)NR1R2, NR1C(O)R2, NR1C(O)OR2, halogen, cyano and nitro, and also oxides (e.g. =O, -O~ or -OH);
wherein each R1 - R5 is independently selected from the group consisting of:
(a) hydrogen, (b) C1-C6 alkyl, preferably, C1-C5 linear, branched, or cyclic alkyl, wherein said alkyl is optionally substituted with halogen up to per-halo;
(c) phenyl;
(d) 5-6 membered monocyclic heteroaryl having 1-4 heteroatoms selected from the group consisting of O, N and S or 8-10 membered bicyclic heteroaryl having 1-6 heteroatoms selected from the group consisting of O, N and S;
(e) C1-C3 alkyl-phenyl wherein said alkyl moiety is optionally substituted with halogen up to per-halo; and (f) C1-C3 alkyl-heteroaryl having 1-4 heteroatoms selected from the group consisting of O, N and S, wherein said heteroaryl group is a 5-6 membered monocyclic heteroaryl or a 8-10 membered bicyclic heteroaryl, and wherein said alkyl moiety is optionally substituted with halogen up to per-halo, wherein each R1 - R5, when not hydrogen is optionally substituted with 1-3 substituents independently selected from the group consisting of C1-C5 linear branched or cyclic alkyl, wherein said alkyl is optionally substituted with halogen up to per-halo, C1-C3 alkoxy, wherein said alkoxy is optionally substituted with halogen up to per-halo, hydroxy, amino, C1-C3 alkylamino, C2-C6 dialkylamino, halogen, cyano, and nitro; and each variable q is independently selected from 0, 1, or 2.
2. A method of claim 1 wherein A, B, and M are each, independently, (i) a substituted or unsubstituted monocyclic heteroaryl group selected from the group consisting of:
2- and 3-furyl, 2- and 3-thienyl, 2- and 4-triazinyl, 1-, 2- and 3-pyrrolyl, 1-, 2-, 4- and 5-imidazolyl, 1-, 3-, 4- and 5-pyrazolyl, 2-, 4- and 5-oxazolyl, 3-, 4- and 5-isoxazolyl, 2-, 4- and 5-thiazolyl, 3-, 4- and 5-isothiazolyl, 2-, 3- and 4-pyridyl, 2-, 4-, 5- and 6-pyrimidinyl,1,2,3-triazol-1-, -4- and-5-yl, 1,2,4-triazol-1-, -3- and -5-yl, 1- and 5-tetrazolyl, 1,2,3-oxadiazol-4- and-5-yl, 1,2,4-oxadiazol-3- and -5-yl, 1,3,4-thiadiazol-2- and-5-yl, 1,2,4-oxadiazol-3-and -5-yl, 1,3,4-thiadiazol-2- and-5-yl, 1,3,4-thiadiazol-3- and -5-yl, 1,2,3-thiadiazol-4- and -5-yl, 2-, 3-, 4-, 5-and 6-2H-thiopyranyl, 2-, 3- and 4-4H-thiopyranyl, 3- and 4-pyridazinyl, 2-,3-pyrazinyl, (ii) a substituted or unsubstituted bicyclic heteroaryl groups selected from the group consisting of:
benzofuryl, benzothienyl, indolyl, benzimidazolyl, benzopyrazolyl, benzoxazolyl;
benzisoxazolyl, benzothiazolyl, benzisothiazolyl, benz-1,3-oxadiazolyl, quinolinyl, isoquinolinyl, quinazolinyl, tetrahydroquinolinyl, tetrahydroisoquinolinyl, dihydrobenzofuryl, pyrazolo[3,4-b]pyrimidinyl, purinyl, benzodiazine, pterindinyl, pyrrolo[2,3-b]pyridinyl, pyrazolo[3,4-b]pyridinyl, oxazo[4,5-b]pyridinyl, imidazo[4,5-b]pyridinyl, cyclopentenopyridine, cyclohexanopyridine, cyclopentanopyrimidine, cyclohexanopyrimidine, cyclcopentanopyrazine, cyclohexanopyrazine, cyclopentanopyridiazine, cyclohexanopyridazine, cyclopentanoimidazole, cyclohexanoimidazole, cyclopentanothiophene and cyclohexanothiophene, or (iii) a substituted or unsubstituted aryl group without heteroatoms selected from the group consisting of:

phenyl, 1-naphthyl, 2-naphthyl, tetrahydronaphthyl, indanyl, indenyl, benzocyclobutanyl, benzocycloheptanyl and benzocycloheptenyl.
3. A method as in claim 2 wherein the substituents on the groups for A, B, and M are selected from the group consisting of: methyl, ethyl, propyl, butyl, pentyl, isopropyl, isobutyl, sec-butyl, and tert-butyl, F, Cl, Br, and I.
4. A method of claim 1 wherein the saturated monocyclic and bicyclic carbocyclic moieties are selected from the group consisting of cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, and decahydronapthalene, the partially saturated monocyclic and bicyclic carbocyclic moieties are selected from the group consisting of cyclopentenyl, cyclohexenyl, cyclohexadienyl and tetrahydronaphthalene, the saturated monocyclic and bicyclic heterocyclic moieties are selected from the group consisting of include tetrahydropyranyl, tetrahydrofuranyl, 1,3-dioxolane, 1,4-dioxanyl, morpholinyl, thiomorpholinyl, piperazinyl, piperidinyl, piperidinonyl, tetrahydropyrimidonyl, pentamethylene sulfide and tetramethylene sulfide and the partially saturated monocyclic and bicyclic heterocyclic moieties are selected from the group consisting of dihydropyranyl, dihydrofuranyl, dihydrothienyl, dihydropiperidinyl, and dihydropyrimidonyl.
5. A method of claim 1 wherein the structures of A, B and M are each independently selected from the group consisting of optionally substituted phenyl, naphthyl, furyl, isoindolinyl, oxadiazolyl, oxazolyl, isooxazolyl, pyrazolyl, pyridinyl, pyrimidinyl, pyrrolyl, quinolinyl, isoquinolinyl, tetrazolyl, thiadiazolyl, thiazolyl and thienyl.
6. A method of claim 5 wherein the substituents of the substituted structures of B are each, independently, selected from the group consisting of methyl, trifluoromethyl, ethyl, n-propyl, n-butyl, n-pentyl, isopropyl, isobutyl, sec-butyl, tent-butyl, cyclopropyl, cyclobutyl, cyclopentyl, methoxy, ethoxy, propoxy, Cl, Br and F, cyano, nitro, hydroxy, amino, methylamino, dimethylamino, ethylamino, diethylamino and the stricture , -L-M.
7. A method of claim 5 wherein the substituents of the substituted structures of A and M
are each, independently, selected from the group consisting of methyl, trifluoromethyl, ethyl, n-propyl, n-butyl, n-pentyl, isopropyl, tert-butyl, sec-butyl, isobutyl, cyclopropyl, cyclobutyl, cyclopentyl, methoxy, ethoxy, propoxy, Cl, Br and F, cyano, nitro, hydroxy, amino, methylamino, dimethylamino, ethylamino and diethylamino and further include:
phenyl, pyridinyl, pyrimidinyl, chlorophenyl, dichlorophenyl, bromophenyl, dibromophenyl, chloropyridinyl, bromopyridinyl, dichloropyridinyl, dibromopyridinyl methylphenyl, methylpyridinyl quinolinyl, isoquinolinyl, isoindolinyl, pyrazinyl, pyridazinyl, pyrrolinyl, imidazolinyl, thienyl, furyl, isoxazolinyl, isothiazolinyl, benzopyridinyl, benzothiazolyl, C1-C5 acyl;
NH(C1-C5 alkyl, phenyl or pyridinyl), such as aminophenyl;
N(C1-C5 alkyl)(C1-C5 alkyl, phenyl or pyridinyl), such as diethylamino and dimethyl amino;
S(O)q(C1-C5 alkyl); such as methanesulfonyl;
S(O)q H;
SO2NH2;
SO2NH(C1-C5 alkyl);
SO2N(C1-C5 alkyl)(C1-C5 alkyl);
NHSO2(C1-C5 alkyl); N(C1-C3 alkyl) SO2(C1-C5 alkyl);
CO(C1-C6 alkyl or phenyl);
C(O)H;
C(O)O(C1-C6 alkyl or phenyl), such as C(O)OCH3, -C(O)OCH2CH3, -C(O)OCH2CH2CH3;
C(O)OH;
C(O)NH2 (carbamoyl);
C(O)NH(C1-C6 alkyl or phenyl) such as N-methylethyl carbamoyl, N-methyl carbamoyl, N-ethylcarbamoyl, or N-dimethylamino ethyl carbamoyl;
C(O)N(C1-C6 alkyl or phenyl)(C1-C6 alkyl, phenyl or pyridinyl), such as N-dimethyl carbamoyl;
C(N(C1-C5 alkyl)) (C1-C5 alkyl);
NHC(O)(C1-C6 alkyl or phenyl) and N(C1-C5 alkyl,)C(O)(C1-C5 alkyl).
wherein each of the above substituents is optionally partially or fully halogenated.
8. A method as in claim 1 wherein A, B or M of formula I or a combination thereof are independently selected from the group consisting of substituted or unsubstituted phenyl, pyridinyl, naphthyl, quinolinyl and isoquinolinyl.
9. A method as in claim .l wherein A, B or M of formula I or a combination thereof are independently a phenyl or pyridinyl group, optionally substituted by halogen up to per halo and 0 s to 3 times by one or more substituent is selected from the group consisting of -CN, C1-C5 alkyl, C1-C5 alkoxy, -OH, phenyl, up to per halo substituted C1-C5 alkyl, up to per halo substituted Ct-C5 alkoxy and up to per halo substituted phenyl.
10. A method as in claim 1 wherein A, B and M of formula I follow one of the following combinations:
A=phenyl, B=phenyl and M is phenyl, pyridinyl, quinolinyl, isoquinolinyl or not present, A=phenyl, B=pyridinyl and M is phenyl, pyridinyl, quinolinyl, isoquinolinyl or not present, A=phenyl, B = naphthyl and M is phenyl, pyridinyl, quinolinyl, isoquinolinyl or not present, A=pyridinyl, B= phenyl and M is phenyl, pyridinyl, quinolinyl, isoquinolinyl or not present, A=pyridinyl, B= pyridinyl and M is phenyl, pyridinyl, quinolinyl, isoquinolinyl or not present, A=pyridinyl, B= naphthyl and M is phenyl, pyridinyl, quinolinyl, isoquinolinyl or not present, A=isoquinolinyl, B=phenyl and M is phenyl, pyridinyl, quinolinyl, isoquinolinyl or not present, A= isoquinolinyl, B=pyridinyl and M is phenyl, pyridinyl, quinolinyl, isoquinolinyl or not present, A= isoquinolinyl, B= naphthyl and M is phenyl, pyridinyl, quinolinyl, isoquinolinyl or not present, page 70 A= quinolinyl, B=.phenyl and.M is phenyl, pyridinyl, quinolinyl, isoquinolinyl or not present, A= quinolinyl, B=pyridinyl and M is phenyl, pyridinyl, quinolinyl, isoquinolinyl or not present, A= quinolinyl, B=naphthyl and M is phenyl, pyridinyl, quinolinyl, isoquinolinyl or not present.
11. A method as in claim 10 wherein L of formula I is -O-, a single bond, -S-, -NH-, -N(CH3)-, -NHCH2-, -NC2H4-, -CH2-, -C(O)-, -CH(OH)-, NHC(O)N(CH3)CH2-, -N(CH3)C(O)N(CH3)CH2-, -CH2C(O)N(CH3)-, -C(O)N(CH3)CH2-; -NHC(O)-, -N(CH3)C(O)-, -C(O)N(CH3)-, -C(O)NH-, -CH2O-, -CH2S-, -CH2N(CH3)-, -OCH2-, -CHF-, -CF2-,-CCl2-, -S-CH2- , and N(CH3)CH2-,
12. A method as in claim 1 wherein the disease is mediated by the VEGF-induced signal transduction pathway.
13. A method as in claim 12 wherein disease mediated by the VEGF-induced signal transduction pathway that is treated is characterized by abnormal angiogenesis or hyperpermiability processes.
14. A method as in claim 13 wherein a compound of Formula I, a salt form of a compound of Formula I, an isolated stereo-isomer of a compound of Formula I or a prodrug of a compound of Formula I is administered simultaneously with another angiogenesis inhibiting agent to a patient with such a disorder in the same formulation or in separate formulations.
15. A method as in claim 1 wherein the disease that is treated is one or more of the following conditions in humans and/or other mammals: tumor growth, retinopathy, ischemic retinal-vein occlusion, retinopathy of prematurity, age related macular degeneration; rheumatoid arthritis, psoriasis, a bolos disorder associated with subepidermal blister formation, including bullous pemphigoid, erythema multiforme, or dermatitis herpetiformis.
16. A method as in claim 1 wherein the disease that is treated is one or more of the following conditions in humans and/or other mammals: tumor growth, retinopathy, ischemic retinal-vein occlusion, retinopathy of prematurity, age related macular degeneration; rheumatoid arthritis, psoriasis, a bullous disorder associated with subepidermal blister formation, including bullous pemphigoid, erythema multiforme, or dermatitis herpetiformis in combination with another condition selected from the group consisting of:
rheumatic fever, bone resorption, postmenopausal osteoporosis, sepsis, gram negative sepsis, septic shock, endotoxic shock, toxic shock syndrome, systemic inflammatory response syndrome, inflammatory bowel disease (Crohn's disease and ulcerative colitis), Jarisch-Herxheimer reaction, asthma, adult respiratory distress syndrome, acute pulmonary fibrotic disease, pulmonary sarcoidosis, allergic respiratory disease, silicosis, coal worker's pneumoconiosis, alveolar injury, hepatic failure, liver disease during acute inflammation, severe alcoholic hepatitis, malaria (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 (demyelation and oligiodendrocyte loss in multiple sclerosis), advanced cancer, lymphoid malignancy, pancreatitis, impaired wound healing in infection, inflammation and cancer, myelodysplastic syndromes, systemic lupus erythematosus, biliary cirrhosis, bowel necrosis, radiation injury] toxicity following administration of monoclonal antibodies, host-versus-graft reaction (ischemia reperfusion injury and allograft rejections of kidney, liver, heart, and skin), lung allogra$ rejection (obliterative bronchitis) and complications due to total hip replacement.
17. A method as in claim 1 wherein the disease that is treated is one or more of the following conditions in humans and/or other mammals:
tumor growth, retinopathy, diabetic retinopathy, ischemic retinal-vein occlusion, retinopathy o.f prematurity, age related macular degeneration; rheumatoid arthritis, psoriasis, bullous disorder associated with subepidermal blister formation, bullous pemphigoid, erythema multiforme, and dermatitis herpetiformis, in combination with an infectious disease selected from the group consisting of:
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 burgdarferi, Treponema pallidum, cytomegalovirus, influenza virus, Theiler's encephalomyelitis virus, and the human immunodeficiency virus (HTV).
18. A method as in claim 1, wherein M is substituted by at Ieast one substituent selected from the group consisting of S(O)q R1, SO2NR1R2, C(O)R1, C(O)OR1, C(O)NR1R2, wherein q, R1 and R2 are independently as defined in claim 1.
19. A method as in claim 1, wherein M is substituted by at least one substituent selected from the group consisting of -C(O)R1, C(O)OR1, and C(O)NR1R2, wherein-R1 and R2 are independently as defined in claim I.
20. A method of claim 1 wherein M is substituted by -C(O) NR1R2, wherein R1 and R2 are independently as defined in claim 1.
21. A method of treating diseases mediated by the VEGF-induced signal transduction pathway comprising administering the compound N-(4-chloro-3-(trifluoromethyl)phenyl)-N'-(4-(2-(N methylcarbamoyl)-4-pyridyloxy)phenyl) urea of the formula below or a pharmaceutically acceptable salt thereof
22. A method of treating diseases mediated by the VEGF-induced signal transduction pathway comprising administering the compound N-(4-chloro-3-(trifluoromethyl)phenyl)-N'-(4-(2-(N-methylcarbamoyl)-4-pyridyloxy)phenyl) urea tosylate.
23: A method of claim 1 wherein the structures of A, B and M are each, independently selected from the group consisting of phenyl, substituted phenyl, pyridinyl, substituted pyridinyl, pyrimidinyl, substituted pyrimidinyl, naphthyl substituted naphthyl, isoquinolinyl, .substituted isoquinolinyl, quinolinyl and substituted quinolinyl.
24. A method as in claim 23, wherein M is substituted by at least one substituent selected from the group consisting of S(O)q R1, SO2NR1R2, C(O)R1, C(O)OR1, C(O)NR1R2, wherein q, R1 and R2 are independently as defined in claim 1.
25. A method of claim 14 wherein M is additionally substituted 1 to 3 tunes by one or more substituents selected from the group consisting of C1-C10 alkyl, up to per halo substituted C1-C10 alkyl, -CN, -OH, halogen, C1-C10 alkoxy and up to per halo substituted C1-C10 alkoxy.
26. A method as in claim 1 wherein L of formula I is -O-, a single bond, -S-, -NH-, N(CH3)-, -NHCH2-, -NC2H4-, -CH2-, -C(O)-, -CH(OH)-, -NHC(O)N(CH3)CH2-, -NCH3C(O)N(CH3)CH2-, -CH2C(O)N(CH3)-, C(O)N(CH3)CH2-, -NHC(O)=, -N(CH3)C(O)-, -C(O)N(CH3)-, -C(O)NH-, -CH2O-, -CH2S-, -CH2N(CH3)-, -OCH2-, -CHF-, -CF2-,-CCl2-, -S-CH2- or -N(CH3)CH2- .
27. A method of claim 1 wherein L of formula I is selected from the group consisting of -O-, -S-, -N(R35)-, -(CH2)m-, -C(O)-, -CH(OH)-, -(CH2)m O, where m= 1-3 and R35 is hydrogen, C1-C10 alkyl, up to per-halo substituted C1-C10 alkyl, -CN, -OH, halogen, C1-C10 alkoxy or up to per halo substituted C1-C10 alkoxy.
28. A method of claim 2 wherein M is substituted by -C(O)NR1R2 and R1 and R2 are as defined in claim 1.
29. A method of claim 1 wherein M is a saturated C3-C6 monocyclic carbocyclic moiety. selected from the group consisting of cyclopropyl, cyclobutyl, cyclopentanyl, and cyclohexanyl;
a saturated C8-C10 bicyclic carbocyclic moiety selected from the group consisting of bicyclopentanyl and bicyclohexanyl;
a partially saturated C3-C6 monocyclic carbocyclic moiety selected from the group consisting of cyclopentenyl, cyclohexenyl and cyclohexadienyl;
the partially saturated C8-C10 bicyclic carbocyclic moiety bicyclohexenyl;

a substituted naphthyl group selected from benzocyclobutanyl, indanyl, indenyl, dihydronaphthyl and tetrahydronaphthyl; or an 8 to 10 membered bicyclic heteroaryl group selected from cyclopentenopyridine, cyclohexanopyridine, - cyclopentanopyrimidine, cyclohexanopyrimidine, cyclcopentanopyrazine, cyclohexanopyrazine, cyclopentanopyridiazine, cyclohexanopyridazine, cyclopentanothiophene and cyclohexanothiophene.
30. A method as in claim 12 wherein the disease that is treated or prevented is a KDR-mediated disorder.
31. A method as in claim 12 wherein the disease that is treated or prevented is a Flk-1 mediated disorder.
32. A method of regulating tyrosine kinase signal transduction comprising administering to a human or other mammal one or more compounds of claim 1.
33. A method for treating or preventing a disease in a human or other mammal regulated by tyrosine kinase, (associated with an aberration in the tyrosine kinase signal transduction pathway) comprising administering to a human or other mammal in need thereof a compound of Formula I, a salt form of a compound of Formula I, an isomer of a compound of Formula I or a prodrug of a compound of Formula I

A-NH-C(O)-NH-B

wherein A is selected from the group consisting of (i) a substituted or unsubstituted monocyclic heteroaryl group selected from the group consisting of:

page 75 2- and 4-triazinyl, 1-, 2- and 3-pyrrolyl, 1-, 2-, 4- and 5-imidazolyl, 3-, 4-and 5-isothiazolyl, 2-, 4-, 5- and 6-pyrimidinyl, 1,2,3-triazol-1-, -4- and -5-yl, 1,2,4-triazol-1-, -3- and -5-yl, 1,2,3-oxadiazol-4- and -5-yl, 1,2,4-oxadiazol-3- and -5-yl, 1,3,4-thiadiazol-2- and -5-yl, 2-, 3-,4-,5- and 6-2H-thiopyranyl, 2-, 3- and 4-4H-thiopyranyl, 3- and 4-pyridazinyl, 2-,3-pyrazinyl, (ii) a substituted or unsubstituted bicyclic heteroaryl groups selected from the group consisting of:
benzofuryl, benzopyrazolyl, benzoxazolyl, benzisoxazolyl, benzothiazolyl, benzisothiazolyl, bent-1,3-oxadiazolyl, quinolinyl, isoquinolinyl, quinazolinyl, tetrahydroquinolinyl, tetrahydroisoquinolinyl, dihydrobenzofuryl, pyrazolo[3,4-b]pyrimidinyl, purinyl, benzodiazine, pterindinyl, pyrrolo[2,3-b]pyridinyl, pyrazolo[3,4-b]pyridinyl, oxazo[4,5-b]pyridinyl, imidazo[4,5-b]pyridinyl, cyclopentenopyridine, cyclohexanopyridine, cyclopentanopyrimidine, cyclohexanopyrimidine, cyclcopentanopyrazine, cyclohexanopyrazine, cyclopentanopyridiazine, cyclohexanopyridazine, cyclopentanoimidazole, cyclohexanoimidazole, cyclopentanothiophene and cyclohexanothiophene, or (iii) substituted or unsubstituted aryl group without heteroatoms selected from the group consisting of:
tetrahydronaphthyl, indanyl, indenyl, benzocyclobutanyl, benzocycloheptanyl and benzocycloheptenyl, B is selected from the group consisting of (i) a substituted or unsubstituted monocyclic heteroaryl group selected from the group consisting of:
2- and 4-triazinyl, 1-, 2- and 3-pyrrolyl, 1-, 2-, 4- and 5-imidazolyl, 3-, 4-and 5-isothiazolyl, 2-, 4-, 5- and 6-pyrimidinyl, 1,2,3-triazol-1-, -4- and -5-yl, 1,2,4-triazol-1-, -3- and -5-yl, 1,2,3-oxadiazol-4- and -5-yl, 1,2,4-oxadiazol-3- and -5-yl, 1,3,4-thiadiazol-2- and -5-yl, 2-, 3-, 4-, 5- and 6-2H-thiopyranyl, 2-, 3- and 4-4H-thiopyranyl, 3- and 4-pyridazinyl, 2-,3-pyrazinyl, (ii) a substituted or unsubstituted bicyclic heteroaryl groups selected from the group consisting of:
benzofuryl, benzopyrazolyl, benzoxazolyl, benziosoxazolyl, benzothiazolyl, benziosothiazolyl, benz-1,3-oxadiazolyl, quinolinyl, isoquinolinyl, quinazolinyl, tetrahydroquinolinyl, tetrahydroisoquinolinyl, dihydrobenzofuryl, pyrazolo[3,4-b]pyrimidinyl, purinyl, benzodiazine, pterindinyl, pyrrolo[2,3-b]pyridinyl, pyrazolo[3,4-b]pyridinyl, oxazo[4,5-b]pyridinyl, imidazo[4,5-b]pyridinyl, cyclopentenopyridine, cyclohexanopyridine, cyclopentanopyrimidine, cyclohexanopyrimidine, cyclcopentanopyrazine, cyclohexanopyrazine, cyclopentanopyridiazine, cyclohexanopyridazine, cyclopentanoimidazole, cyclohexanoimidazone, cyclopentanothiophene and cyclohexanothiophene, or (iii) a substituted or unsubstituted aryl group without heteroatoms selected from 1 group consisting of:
tetrahydronaphthyl, indanyl, indenyl, benzocyclobutanyl, benzocycloheptanyl and benzocycloheptenyl, wherein the groups A and B are optionally substituted with 1-3 substituents independently selected from the group consisting of -L-M, L is selected from the group consisting of:

(a) -(CH2)m-O-(CH2)l-, (b) -(CH2)m-(CH2)l-, (c) -(CH2)m-C(O)-(CH2)l-, (d) -(CH2)m-NR3-(CH2)l-, (e) -(CH2)m-NR3C(O)-(CH2)l-, (f) -(CH2)m-S-(CH2)l-, (g) -(CH2)m-C(O)NR3-(CH2)l-, (h) -(CH2)m-CF2-(CH2)l-, (i) -(CH2)m-CCl2-(CH2)l-, (j) -(CH2)m-CHF-(CH2)l-, (k) -(CH2)m-CH(OH)-(CH2)l-;
(l) -(CH2)m-C.ident.C-(CH2)l-;
(m) -(CH2)m-C=C-(CH2)l-; and (n) a single bond, where m and 1 are 0;
(o) -(CH2)m-CR4R5-(CH2)l-;

where the variables m and 1 are integers independently selected from 0-4, M is selected from the group consisting of:
(i) phenyl, optionally substituted with 1-3 substituents independently selected from the group consisting of R1, OR1, NR1R2, S(O)q R1, SO2NR1R2, NR1SO2R2, C(O)R1, C(O)OR1, C(O)NR1R2, NR1C(O)R2, NR1C(O)OR2, halogen, cyano and nitro;
(ii) naphthyl, optionally substituted with 1-3 substituents independently selected from the group consisting of R1, OR1, NR1R2, S(O)q R1, SO2NR1R2, NR1SO2R2, C(O)R1, C(O)OR1, C(O)NR1R2, NR1C(O)R2, NR1C(O)OR2, halogen, cyano and nitro;

(iii) 5 and 6 membered monocyclic heteroaryl groups, having 1-3 heteroatoms independently selected from the group consisting of O, N and S, optionally substituted with 1-3 substituents independently selected from the group consisting of R1, OR1, NR1R2, S(O)q R1, SO2NR1R2, NR1SO2R2, C(O)R1, C(O)OR1, C(O)NR1R2, NR1C(O)R2, NR1C(O)OR2, halogen, cyano and nitro and also oxides (e.g. =O, -O~ or -OH-); and (iv) 8 to 10 membered bicyclic heteroaryl groups, having 1-6 heteroatoms independently selected from the group consisting of O, N and S, optionally substituted with 1-3 substituents independently selected from the group consisting of R1, OR1, NR1R2, S(O)q R1, SO2NR1R2, NR1SO2R2, C(O)R1, C(O)OR1, C(O)NR1R2, NR1C(O)R2, NR1C(O)OR2, halogen, cyano and nitro and also oxides (e.g. =O, -O~ or -OH).
(v) saturated and partially saturated C3-C6 monocyclic carbocyclic moiety optionally substituted with 1-3 substituents independently selected from the group consisting of R1, OR1, NR1R2, S(O)q R1, SO2NR1R2, NR1SO2R2, C(O)R1, C(O)OR1, C(O)NR1R2, NR1C(O)R2, NR1C(O)OR2, halogen, cyano and, nitro;
(vi) saturated and partially saturated C8-C10 bicyclic carbocyclic moiety, optionally substituted with 1-3 substitutents independently selected from the group consisting of R1, OR1, NR1R2, S(O)q R1, SO2NR1R2, NR1SO2R2, C(O)R1, C(O)OR1, C(O)NR1R2, NR1C(O)R2, NR1C(O)OR2, halogen, cyano and nitro;
(vii) saturated and partially saturated 5 and 6 membered monocyclic heterocyclic moiety, having 1-3 heteroatoms independently selected from the group consisting of O, N and S, optionally substituted with 1-3 substituents independently selected from the group consisting of R1, OR1, NR1R2, S(O)q R1, SO2NR1R2, NR1SO2R2, C(O)R1, C(O)OR1, C(O)NR1R2, NR1C(O)R2, NR1C(O)OR2, halogen, cyano and nitro, and also oxides (e.g. =O, -O~ or -OH);
and (viii) saturated and partially saturated 8 to 10 membered bicyclic heterocyclic moiety, having 1-6 heteroatoms independently selected from the group consisting of O, N and S, optionally substituted with 1-3 substituents independently selected from the group consisting of R1, OR1, NR1R2, S(O)q R1, SO2NR1R2, NR1SO2R2, C(O)R1, C(O)OR1, C(O)NR1R2, NR1C(O)R2, NR1C(O)OR2, halogen, cyano and nitro, and also oxides (e.g. =O, -O~ or -OH);
wherein each R1-R5 is independently selected from the group consisting of:
(a) hydrogen, (b) C1-C6 alkyl, preferably, C1-C5 linear, branched, or cyclic alkyl, wherein said alkyl is optionally substituted with halogen up to per-halo;
(c) phenyl;

(d) 5-6 membered monocyclic heteroaryl having 1-4 heteroatoms selected from the group consisting of O, N and S or 8-10 membered bicyclic heteroaryl having 1-6 heteroatoms selected from the group consisting of O, N and S;
(e) C1-C3 alkyl-phenyl wherein said alkyl moiety is optionally substituted with halogen up to per-halo; and (f) C1-C3 alkyl-heteroaryl having 1-4 heteroatoms selected from the group consisting of O, N and S, wherein said heteroaryl group is a 5-6 membered monocyclic heteroaryl or a 8-10 membered bicyclic heteroaryl, and wherein said alkyl moiety is optionally substituted with halogen up to per-halo;
wherein each R1-R5, when not hydrogen is optionally substituted with 1-3 substituents independently selected from the group consisting of C1-C5 linear, branched or cyclic alkyl, wherein said alkyl is optionally substituted with halogen up to per-halo, C1-C3 alkoxy, wherein said alkoxy is optionally substituted with halogen up to per-halo, hydroxy, amino, C1-C3 alkylamino, C2-C6 dialkylamino, halogen, cyano, and nitro; and each variable q is independently selected from 0, 1, or 2.
34. A method of claim 1 wherein the structures of A, B and M are each independently selected from the group consisting of optionally substituted isoindolinyl, oxadiazolyl, pyrimidinyl, pyrrolyl, quinolinyl, and isoquinolinyl.
35. A method as in claim 1 wherein A, B or M of formula I or a combination thereof are independently selected from the group consisting of substituted or unsubstituted quinolinyl and isoquinolinyl.
36. A method as in claim 1 wherein A, B or M of formula I follow one of the following combinations:
A=pyridinyl, B=pyridinyl and M is phenyl, pyridinyl, quinolinyl, isoquinolinyl or not present, A=pyridinyl, B=naphthyl and M is phenyl, pyridinyl, quinolinyl, isoquinolinyl or not present, A=isoquinolinyl, B=phenyl and M is phenyl, pyridinyl, quinolinyl, isoquinolinyl or not present, A=isoquinolinyl, B=pyridinyl and M is phenyl, pyridinyl, quinolinyl, isoquinolinyl or not present, A=isoquinolinyl, B=naphthyl and M is phenyl, pyridinyl, quinolinyl, isoquinolinyl or not present, A=quinolinyl, B=phenyl and M is phenyl, pyridinyl, quinolinyl, isoquinolinyl or not present, A=quinolinyl, B=pyridinyl and M is phenyl, pyridinyl, quinolinyl, isoquinolinyl or not present, A=quinolinyl, B=naphthyl and M is phenyl pyridinyl, quinolinyl, isoquinolinyl or not present.
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