WO2001053299A1 - Compounds of the saframycin-ecteinascidin series, uses, and synthesis thereof - Google Patents

Abstract

Compounds of the saframycin-ecteinascidin series with cytotoxic properties having the general formula (1), their uses and synthesis, are disclosed. In said formula, R1 and R4 is H, a C1 to C4 alkyl group, or an acyl group; R2 is an ether, ester, amide, or a phthalimide group; R3 is =O, OH, an ether group, an acyl group such as OC(O)Me, OC(O)Bn and OC(O)Et, or a sulfide group; R5 is H, halogen, OH, an ether group, an acyl group, or an amide group; R6 is =O, OH, OCH3, CN, or an acyfoxy group; wherein R7 is =0, OH, halogen, an ether group, or an acyl group; wherein R8 and R9 are independently H, CH3, OCH3 OC2H5, CF3, halogen such as Br and F, or R8 and R9 are joined together as a methylenedioxy group, or other five or six membered ring; R10 and R11 are independently CH3, OCH3, OC2H5, SCH3, or SC2H5; R12 is H, a C1 to C4 alkyl group, or an acyl group; and the chiral center marked * has the R or the S configuration.

Description

COMPOUNDS OF THE SAFRAMYCIN-ECTEINASCIDIN SERIES, USES, AND SYNTHESIS THEREOF ~ ^"" ~~

This application claims the benefit of U.S. Provisional Application No. 60/177,071, filed January 19, 2000.

This invention has been made with government support under National Institutes of Health Grant Nos. CA-28824 and HL-25848. Accordingly, the U.S. Government may have certain rights in the invention.

Throughout this application, various publications may be referenced by Arabic numerals in brackets. Full citations for these publications may be found at the end of the specification immediately preceding the claims. The disclosures of these publications in their entireties are hereby incorporated by reference into this application in order to more fully describe the state of the art as known to those skilled therein as of the date of the invention described and claimed herein.

Field of Invention

The disclosed invention relates to novel compounds of the saframycin-ecteinascidin series having cytotoxic properties and to schemes for the total synthesis of such compounds.

Background of the Invention

The screening of natural product sources for new drug candidates with useful therapeutic margins has led to a variety of novel structures. One of the most fascinating and promising of these is ecteinascidin 743 (ET 743) derived from the marine tunicate Ecteinascidia turbina ta . (1) The novel structure of Et 743, its difficult availability, and its exceedingly potent cytotoxicity render it an attractive target for total synthesis. This goal was undertaken and accomplished in a most interesting fashion by E. J. Corey and coworkers . (2) Follow-up studies by Corey, Schreiber (3) and co-workers resulted in the demonstration that a significantly simplified version of ET 743 (ie: phthalascidin) retains the cytotoxicity of the natural product. Previously, well before the ecteinascidins were known, some of the named inventors had accomplished what was then the only total synthesis of quinocarcinol . (4 ) The central Mannich-like envelopment strategy, learned from work in the quinocarcin series, was adapted to the ET problem.

While ET 743 was previously known, the total synthesis of ET 743 was first accomplished by Corey in 1996 and, prior to this invention, was the only total synthesis of an ecteinascidin.

It is known that saframycin B, saframycin A (13,14), saframycin S (15), ecteinascidin 729 (Et 729) (16), Et 743 and Phthalascidin (3) all posses cytotoxic antitumor and antibiotic characteristics. It is also known that saframycin S, saframycin B, saframycin A, Et 729, Et 743 (17), and phthalascidin (3) all possess a two tetrahydroisoquinoline aromatic carbon nitrogen framework. Saframycins and ecteinascidins have been shown to interact with DNA. Interactions are believed to occur between DNA and the tetrahydroisoquinoline aromatic carbon nitrogen framework. (2,18)

gnτπmar-γ of the Invention

The subject invention provides compounds of the saframycin- ecteinascidin series with cytotoxic properties having the following general formula, their uses and synthesis:

wherein R_x and R„ is H, a C_: to C₄ alkyl group, or an acyl group; wherein R₂ is an ether, ester, amide, a phthalimide group, a substituted phthalimide group or is covalently bound to R₆; wherein R₃ is =0, OH, an ether group, an acyl group such as 0C(0)Me, 0C(0)Bn and 0C(0)Et, or a sulfide group; wherein R₅ is H, halogen, OH, an ether group, an acyl group, or an amide group; wherein R₆ is =0, OH, 0CH₃, CN, or an acyloxy group or is covalently bound to R₂; wherein R₇, is =0, OH, halogen, an ether group, or an acyl group; wherein R₈ and R₉ are independently H, CH₃, 0CH₃, OC₂H₅, CF₃, halogen such as Br and F, or Re and Rg are joined together as a methylenedioxy group, or other five or six membered ring; wherein R₁₀ and R_n are independently CH₃, 0CH₃, 0C₂H₅, SCH₃, or SCjH_s; wherein R₁₂ is H, a to C₄ alkyl group, or an acyl group; and wherein the chiral center marked * has the R or the S configuration. The subject invention also provides for a group of saframycin- ecteinascidin series compounds with cytotoxic properties having the following general formula, their uses and synthesis:

wherein Rj and R₄ is H, a C_: to C₄ alkyl group, or an acyl group; wherein R₂ is an ether, ester, amide, an aromatic group or is covalently bound to R₆; ; wherein R₃ is =0, OH, an ether group, an acyl group such as OC(0)Me, OC(0)Bn and OC(0)Et, a sulfide group or H; wherein R₅ is H, halogen, OH, an ether group, an acyl group, or an amide group; wherein R₆ is =0, OH, OCH₃, CN, or an acyloxy group or is covalently bound to R₂; wherein R₇, is =0, OH, halogen, an ether group, or an acyl group; wherein R₈ and R_g are independently H, CH₃, 0CH₃, O H_s, CF₃ , halogen such as Br and F, or R₈ and R₉ are joined together as a methylenedioxy group, or other five or six membered ring; wherein R₁₀ and R_u are independently CH₃, 0CH₃, OC₂H₅, SCH₃, or SC₂H₅; wherein R_i2 is H, a Ci to C₄ alkyl group, or an acyl group; and wherein the chiral center marked * has the R or the S configuration. Description of the Figures

Figure 1 shows the structures of Saframycin B and Ecteinascidin 743.

Figure 2 is a Table showing the cytotoxicity, antimetabolism and antimicrobial activity of ET 743.

Figure 3 shows the mechanism for the catalytic activation of ET 743 and alkylation of 6GN2.

Figures 4A, 4B and 4C show the retrosynthesis analysis of ET 743 and Saframycin B.

Figures 5A- and 5B show the enatioselective synthesis of amino acid for the synthesis strategy A of Saframycin B.

Figure 6 shows the enatioselective synthesis of tertahydroisoquinoline, which is used as a subunit in the foregoing synthesis.

Figures ?A and 7B show the coupling strategy for the synthesis strategy A of Saframycin B.

Figures 8A and 8B^lshow the modified synthesis of amino acid for synthesis strategy B of Saframycin B.

Figures 9A and 9B| show the synthesis of the pentasubstituted aromatic system and the tertahydroisoquinoline of ET 743, i.e. the left part of ET 743.

Figure 10A shows the coupling steps for the synthesis strategy B for Saframycin B. Figure 10B shows the cyclization for the synthesis strategy B of Saframycin B.

Figure 11 shows the final steps for the total synthesis of ' Saframycin B.

Figure 12 shows the synthesis for ET 743.

Figure 13 shows the coupling and the cyclization steps in synthesis for ET 743.

Figure 14 shows the ET 743 series cyclization analogs.

Figure 15 shows the plan for the total synthesis of ET 743.

Detailed Description of the Invention

An embodiment of the subject invention provides compounds having the formula :

wherein R_x and R₄ is H, a C to C₄ alkyl group, or an acyl group; wherein R₂ is an ether, ester, amide, a phthalimide group, a substituted phathalimide group or is covalently bound to R₆; wherein R₃ is =0, OH, an ether group, an acyl group, or a sulfide group; wherein R₅ is H, halogen, OH, an ether group, an acyl group, or an amide group; wherein R₆ is =0, OH, 0CH₃, CN, an acyloxy group or is covalently bound to R₂; ; wherein R₇, is =0, OH, halogen, an ether group, or an acyl group; wherein R₈ and R₉ are independently H, CH₃, 0CH₃, OC₂H₅, Br, F, CF₃, or R₈ and R₉ are joined together as a methylenedioxy group, or other five or six membered ring; wherein R₁₀ and R_n are independently CH₃, 0CH₃, OC₂H₅, SCH₃, or

SCH_$; wherein R₁₂ is H, a _λ to C₄ alkyl group, or an acyl group; and wherein the chiral center marked * has the R or the configuration.

In another embodiment, the compound has the formula:

where R_{ι r} R₂, R₃, R₄, R₅, R^, R₇, R_e , and R₉ are as defined above

In yet another embodiment, the compound has the formula:

where R_x, R₂, R₃, R₄, R₅, R₆, and R₇ are as defined above, In preferred embodiments of the immediately preceding formula, R_x is CH₃, R₃ is =0, R₄ is CH₃, R₅ is OCH₃, Rg is =0, and R₇ is H.

In another preferred embodiment of the preceding formula, R_x is _; H, R₃ is =0, R₄ is CH₃, R₅ is 0CH₃, R₆ is =0, and R₇ is H.

In yet another preferred embodiment of the preceding formula, Ri is H, R₃ is =0, R₄ is benzene₃, R₅ is OCH₃, R₆ is =0, and R₇ is H.

In yet another preferred embodiment of the preceding formula, R_τ is H, R₃ is =0, R₄ is H, R₅ is OCH₃, R₆ is =0, and R₇ is H.

In yet another preferred embodiment of the preceding formula, Ri is H, R₃ is =0, R₄ is H, R₅ is H, R₆ is =0, and R₇ is H.

In yet another preferred embodiment of the preceding formula, R₁ is H, R₃ is =0, R₄ is H, R₅ is halogen, Rg is =0, and R₇ is H.

In all of the embodiments, and particularly in the preferred embodiments, R₂ is 0C(0)H, R₂ is H, R₂ is OH, R₂ is -0-benzene, R₂ is OCOCH₃, R₂ is -O-t-butyldimethylsilyl, or R₂ is -0- Pivaloyl.

In yet another embodiment, the compound has the formula;

where R_{l r} R₂, R₃, R₄, R₅, R₆, and R₇ are as defined above.

In preferred embodiments of the immediately preceding formula, Ri is CH₃, R₃ is =0, R₄ is CH₃, Rj is 0CH₃, R₆ is =0, and R, is H.

In another preferred embodiment of the preceding formula, R_: is H, R₃ is =0, R₄ is CH₃, R₅ is 0CH₃, R₆ is =0, and R₇ is H.

In yet another preferred embodiment of the preceding formula, R_: is H, R₃ is =0, R₄ is benzene₃, P^ is 0CH₃, Rg is =0, and R₇ is H.

In yet—another preferred embodiment of the preceding formula, R_x is H, R₃ is =0, R₄ is H, R₅ is 0CH₃, R₆ is =0, and R₇ is H.

In yet another preferred embodiment of the preceding formula, R_x is H, R₃ is =0, R₄ is H, R₅ is H, R₆ is =0, and R₇ is H. In yet another preferred embodiment of the preceding formula, R_x is H, R₃ is =0, R₄ is H, R^ is halogen, R₆ is =0, and R₇ is H.

In all of the embodiments, and particularly in the preferred 5.embodiments, R₂ is 0C(0)H, R₂ is H, R₂ is OH, R₂ is -O-benzene, R₂ is OCOCH₃, R₂ is -O-t-butyldimethylsilyl, or R₂ is -0- Pivaloyl .

The subject invention also provides compounds having the 0 formula:

wherein R_x and R₄ is H, a C_λ to C₄ alkyl group, or an acyl group; wherein R₂ is an ether, ester, amide, or a phthalimide 0 group; wherein R₅ is H, halogen, OH, an ether group, an acyl group, or an amide group; wherein R₆ is =0, OH, 0CH₃, CN, or an acyloxy group; wherein R₇, is =0, OH, halogen, an ether group, or an acyl group; wherein R₈ and Rg are independently H, CH, , OCR,, OQ Α, , Br, F, CF₃, or R₈ and R₉ are joined together as a methylenedioxy group, or other five or six membered ring; wherein R₁₀ and R_u are independently CH₃, OCH₃, OC₂H₅, SCH₃, or SC₂H₅; wherein R₁₂ is H, a C₁ to C₄ alkyl group, or an acyl group.

In another embodiment, the compound has the formula:

where R_{l r} R₂ , R₄ , R₅ , R₆, R₇ , R₈ and R₉ are as def ined above

In a preferred embodiment, the compound has the formula:

where R_{l r} R₂, R₄, R₅, R₆, and R₇ are as defined above.

In preferred embodiments of the immediately preceding formula, R_λ is CH₃, R₄ is CH₃, R₅ is OCH₃, R₆ is =0, and R₇ is H.

In another preferred embodiment of the preceding formula, R_λ is H, R₄ is CH₃, R₅ is OCH₃, R₆ is =0, and R₇ is H.

In yet another preferred embodiment of the preceding formula, Ri is H, R₄ is benzene₃, R₅ is 0CH₃, R₆ is =0, and R₇ is H.

In yet another preferred embodiment of the preceding formula, Ri is H, R„ is H, R₅ is 0CH₃, R₆ is =0, and R₇ is H.

In yet another preferred embodiment of the preceding formula, Ri is H, R₄ is H, R₅ is H, R₆ is =0, and R₇ is H.

In yet another preferred embodiment of the preceding formula, R₁ is H, R₄ is H, R₅ is halogen, R₆ is =0, and R₇ is H .

In all of the embodiments , and particularly in the preferred embodiments , R₂ is OC (0) H, R₂ is H, R₂ is OH, R₂ is -O-benzene , R₂ is 0COCH₃, R₂ is -O- t-butyldimethylsilyl , or R₂ is -0- Pivaloyl .

In another preferred embodiment, the compound has the formula :

where R_l R₂, R₄, R₅, R₆, and R₇ are as defined above.

In preferred embodiments of the immediately preceding formula, R_x is CH₃, R₄ is CH₃, R₅ is 0CH₃, R₆ is =0, and R₇ is H.

In another preferred embodiment of the preceding formula, R_λ is H, R₄ is CH₃, R₅ is 0CH₃, R₆ is =0, and R₇ is H.

In yet another preferred embodiment of the preceding formula, Ri is H, R₄ is benzene₃, R₅ is 0CH₃, R₆ is =0, and R₇ is H. In yet another preferred embodiment of the preceding formula, R_x is H, R₄ is H, R₅ is OCH₃, R₆ is =0, and R₇ is H.

In yet another preferred embodiment of the preceding formula, , R_j. is H, R₄ is H, R₅ is H, R₆ is =0, and R₇ is H.

In yet another preferred embodiment of the preceding formula, R₁ is H, R₄ is H, R₅ is halogen, R₆ is =0, and R₇ is H.

In yet another preferred embodiment of the preceding formula, R₁ is H, R₄ is CH₃, R₅ is CH₃, R₆ is =0, and R₇ is H (Compound 110) .

In all of the embodiments, and particularly in the preferred embodiments, R₂ is 0C(0)H, R₂ is H, R₂ is OH, R₂ is -O-benzene, R₂ is OCOCH₃, R₂ is -0-t-butyldimethylsilyl, or R₂ is -0- Pivaloyl .

The subject invention also provides compounds having the following general formula which are used in the synthesis of compounds within the saframycin-ecteinascidin series:

wherein R₄ is H, a C_x to C₄ alkyl group, or an acyl group; wherein R₅ is H, halogen, OH, an ether group, an acyl group, a sulfide group or an amide group; wherein R is CH₃, OCH₃, OC₂H₅, SCH₃, or SC₂H₅; and wherein R₁₂ is H, a C₁ to C₄ alkyl group, or an acyl group.

In another embodiment, the compound has the formula:

where R₄ and R₅ are defined as above, In a preferred embodiment of the immediately preceding formula, R₄ is CH₃ and R₅ is CH₃ (compound 1) .

In another preferred embodiment of the preceding formula, R₄ is i Benzene and R₅ is H (compound 3).

The subject invention also provides compounds having the following general formula which are used in the synthesis of compounds within the saframycin-ecteinascidin series :

wherein R_: is H, a C_λ to C₄ alkyl group, or an acyl group; wherein R₃ is =0, OH, an ether group, an acyl group, a sulfide group or an amide group; wherein R₈ and R₉ are independently H, CH₃, OCH₃, OC₂H₅, SCH₃,

SC₂H₅, or R₈ and R₉ are joined together to form a five or six membered ring; wherein R₁₀ is CH₃, 0CH₃, OC₂H₅, SCH₃, or SC₂H₅.

In another embodiment, of the immediately preceding formula the compound having the formula:

where R_{l f} R₃ and R₁₀ are defined as above The subject invention also provides compounds having the following general formula which are used in the synthesis of compounds within the saframycin-ecteinascidin series :

wherein R₂ is H, a C_: to C₄ alkyl group, or an acyl group; wherein R₃ is =0, OH, an ether group, an acyl group, a sulfide group, an amide group or H; wherein R₈ and R₉ are independently H, CH₃, OCH₃, OC₂H₅, SCH₃,

SC₂H₅, or R₈ and R₉ are joined together to form a five or six membered ring; wherein R₁₀ is CH₃, OCH₃, OC₂H₅, SCH₃, or SC₂H₅.

In another embodiment, of the immediately preceding formula the compound having the formula:

where R_{l r} R₃ and R₁₀ are defined as above . In yet another preferred embodiment, the compound has the formula:

In yet another preferred embodiment , the compound has the formula :

The subject invention also provides a method of producing the compounds within the saframycin-ecteinascidin series such as compound 1, which method comprises reacting a compound having the formula

with a compound having the formula

wherein R_x and R₄ is H, a C to C₄ alkyl group, or an acyl group; wherein R₃ is =0, OH, an ether group, an acyl group, a sulfide group or an amide group; wherein R₅ is H, halogen, OH, an ether group, an acyl group, or an amide group; wherein R₈ and R₉ are independently H, CH₃, OCH₃, OC₂H₅, Br, F, CF3, or R₈ and R₉ are joined together as a methylenedioxy group, or other five or six membered ring; wherein R₁₀ and R_u are independently CH₃, OCH₃, OC₂H₅, SCH₃, or SC₂H₅; and wherein R₁₂ is H, a C_x to C₄ alkyl group, or an acyl group.

In an embodiment of the preceding method, the reaction is performed in the presence of N, N-bis (2-oxo-3- oxazolidinyl) phosphinic chloride .

In another embodiment of the method, the reaction is performed in the presence of Dess-Martin periodinate. In this embodiment, the reaction is further performed in the presence of CH₂C1₂.

This invention also provides a method of producing the compound 2 above, which comprises reacting compound 1 above with camphor sulfonic acid (CSA) in the presence of toluene.

This invention also provides a method of producing the compound 1 above, which comprises reacting compound 2 above with H₂, 10%Pd/C, Ethanol-ascetic acid in the presence hydrochloric acid.

In another embodiment the subject invention provides for a compound having the formula:

wherein R_x and R₄ is H, a ^ to C₄ alkyl group, or an acyl group; wherein R₂ is an ether, ester, amide, aromatic group or is covalently bound to R₆; wherein R₃ is =0, OH, H, an ether group, an acyl group, or a sulfide group; wherein R₅ is H, halogen, OH, ^_OC₍₂_₆₎ alkyl group, an ether group, an acyl group, or an amide group; wherein R₆ is =0, OH, 0CH₃, CN, or an acyloxy group or is covalently bound to R₂; wherein R₇, is H, =0, OH, 0CH₃, halogen, an ether group, or an acyl group; wherein R₈ and R_s are independently H, CH₃, 0CH₃, OC₂H₅, Br, F,

CF₃, or R₈ and R₉ are joined together as a methylenedioxy group, or other five or six membered ring; wherein R₁₀ and R_u are independently CH₃, 0CH₃, OC₂H₅, SCH₃, or

SC₂H₅; wherein R₁₂ is H, a C_: to C₄ alkyl group, or an acyl group; and wherein the chiral center marked * has the R or the s configuration.

In yet another embodiment the compound has the formula:

wherein R_{l r} R₂, R₃, R₄, R₅, R₆, R₇, R₈, and R₉ are defined as in the preceding formula.

In yet another embodiment, the compound has the formula:

wherein R_l R₂, R₃, R₄, R₅, R₆, and R₇ are defined as in the formula above .

In a preferred embodiment of the immediately preceding formula, Ri is H, R₂ is OH, R₃ is H, R₄ is H, R₅ is H, R_j is =0, and R₇ is H (Compound 113) .

In another preferred embodiment of the preceding formula, R_x is CH₃, R₂ is OH, R₃ is H, R₄ is CH₃, Rg is OCH₃, R_g is H and R₇ is H (Compound 107) .

In yet another preferred embodiment of the preceding formula, R_x is H, R₂ is OH, R₃ is H, R₄ is CH₃, Rg is OCH₃, Rg is =0 and R₇ is H (Compound 104) . In yet another preferred embodiment of the preceding formula, R₁ is H, R₂ and R₆ are joined as an ester bond, R₃ is H, R₄ is CH₃, R₅ is 0CH₃, and R₇ is H (Compound 105) .

In yet another preferred embodiment of the preceding formula, R_x is CH₃ , R₂ and Rg are joined as an ester bond, g is H, R, is CH₃, R₅ is OCH₃, and R₇ is H (Compound 106) .

In another embodiment, the compound has the formula:

wherein R_{l r} R₂, R₃, R₄, R₅, R₆, and R₇ are defined as in the preceding formula.

In a preferred embodiment of the immediately preceding formula, R_x is H, R₂ is OH, R₃ is OH, R₄ is CH₃, R₅ is OCH₃, R₆ is =0, and R₇ is H (Compound 109) . In another preferred embodiment of the preceding formula, R_: is H, R₂ is OH, R₃ is H, R_« is CH₃, Rs is 0CH₃, Rg is =0, and R, is H (Compound 111) .

In yet another preferred embodiment of the preceding formula, R_x is H, R₂ is OH, R₃ is =0, R₄ is CH₃, R₅ is OCH₃, R₆ is =0, and R₇ is H (Compound 108) .

The subject invention also provides for a method of producing compound 3, comprising reacting a compound having the formula A with a compound having the formula C.

In an embodiment of the preceding method, the reaction is performed in the presence of N, N-bis (2-oxo-3- oxazolidinyl) phosphinic chloride.

In another embodiment of the preceding method, the reaction is performed in the presence of Dess-Martin periodinate.

In yet another embodiment of the preceding method, the reaction is further performed in the presence of CH₂C1₂.

In yet another embodiment of the preceding method, the reaction is performed with H₂, 10%Pd/C, Ethanol-ascetic acid in the presence hydrochloric acid.

This invention also provides a method of producing the compound 3 above, which comprises reacting compound 2 above with H₂, 10%Pd/C, Ethanol-ascetic acid in the presence hydrochloric acid.

This invention also provides a method of producing the compound 2 above, which comprises reacting compound 3 above with camphor sulfonic acid (CSA) in the presence of toluene. This invention also provides a pharmaceutical composition for treating a tumor in a subject, which comprises a pharmaceutically effective amount of compound 1 above or compound 2 above or compound 3 above.

This invention also provides a method of inhibiting proliferation of tumor cells which comprises contacting the cells under suitable conditions with an effective amount of compound 1 above or compound 2 above or compound 3 above .

This invention also provides a method of treating a patient having a tumor characterized by proliferation of neoplastic cells which comprises administering to the patient an effective amount of compound 1 above or compound 2 above or compound 3 above. In this method the effective amount may be from about 0.5 mg to about 5 mg per day, preferably from about 1 mg to about 3 mg per day, and most preferably about 2 mg per day.

The abbreviation used throughout this disclosure and in the synthesis schemes are abbreviations commonly used in the art of synthetic chemistry and may be readily found in a synthetic chemistry text book.

The abbreviations used in this disclosure are also provided below:

Ac acetyl BOC t-butoxycarbonyl

DAM di (4-methoxyphenyl) methyl

Dmp dimethylphosphinyl

DMPM 3, 4-dimethoxybenzyl

MOM methoxymethyl PMB or MPM p-methoxybenzyl or p-methoxyphenylmethyl

PMBM p-methoxybenzyloxymethyl

Pv or Piv pivaloyl

TBS or TBDMS t-butyldimethylsilyl

THF tetrahydrofuranyl Tos or Ts p-toluenesulfonyl

BOP-C1 N,N-bis (2-oxo-3-oxazolidinyl)phosphinic chloride

CSA camphorsulfonic acid

DDQ 2, 3-dichloro-5, 6-dicyano-l, -benzoquinone

DIBAL-H diisobutylaluminum hydride DMAP 4-N, N-dimethylaminopyridine

DMF N, N-dimethylformamide

DMPU 1, 3-dimethyl-3, 4, 5, 6-tetrahydro-2 (1H) - pyrimidinone

NBS N-bromosuccinimide

TFA trifluoroacetic acid

This invention will be .better understood from the Experimental Details which follow. However, one skilled in the art will readily appreciate that the specific methods and results discussed are merely illustrative of the invention as described more fully in the claims which follow thereafter. EXPERIMENTAL DETAILS Example 1

Synthetic Explorations in the Saframycin-Ecteinascidin Series:

Construction of Major Chiral Subunits Through Catalytic Asymmetric Induction

We undertook to test a synthesis directed to systems of the 4- Oxy-saframycin type. From the perspective of its two aromatic sectors, 4-Oxy-saframycin can be viewed as more closely related to compounds of the saframycin series (Saframycin B, A , and S) than to ET. (5) Indeed, the aromatic rings in III can be regarded as modified hydroquinone versions of the quinone moieties of saframycin, with the important proviso that III also contains a 4-oxo group. This function, in the context of appropriate aromatic domains, is potentially valuable for synthesizing ET and a new range of analogs thereof.

Saπamyαn S (R = OH)

Referring to Scheme 1, our approach to III contemplated the merger of two moieties, 1 and 2, wherein each component would bear the absolute configuration appropriate to the goal system in high enantiomeric excess. In this experiment, we describe the pathways, which we followed for reaching the key building blocks. Our inquiry was directed to the applicability of catalytic oxidative asymmetric induction to these targets, and was strongly influenced by precedents from Sharpless.(6 a-c)

Scheme 1. a) l.leq. BrCH₂CH=CHCH₂OTBS, 1.5eq. K₂C0₃, CH₃CN, reflux, 5h, 100%; b) l.leq. 30% H₂O₂, cat. Se0₂, t-BuOH, 40°C, 5h, then Et₃N, MeOH, 85%; c) l.leq. MOMC1, 1.5eq. (i-Pr)₂NEt, CH₂C1₂, 80°C, 12h, 100%; ) l.leq. Me₂NPh, toluene, 210°C, 12h, 96%; e) Mel(xs), 1.5eq. K₂C0₃, CH₃CN, reflux, 12h, 87%; f) 1.5eq. TBAF, THF, lh; g) l. leq. PivCl, pyridine-CH₂Cl₂(l:20), 3h; h) 3N HC1, THF-i-PtOH(2.1), 12h, 99% for 3 steps; i) 3eq. Et₂AlCl, (CH₂0)„(xs), CH₂C1₂, 12h, 96%; j) Mel(xs), 1.5eq. K₂C0₃, CHCl₃-MeOH(2:l), reflux, 12 h, 90%; ) 1.2eq. TBSC1, 1.5eq. imidazole, cat. DMAP, CH₂Cl_2l lh, 99%; 1) 2.5eq. DIBAL-H, CH₂C1₂, -78°C, 30min, 94%; m) 8% (D)-DET, 5.6% Ti(OiPr)₄, 2eq. t-BuOOH, m.s. 4A, -20°C, Id, 98% (95% ee); n) 3.5eq. Ti(OiPr)2CN3)₂, PhH, 80°C, 76%(single iso er); o) DMP-acetone(l:2), cat. p-TsOHH₂0, lOmin, 100%; p) H-, Pd/C, EtOAc, 1.2eq. (Boc)₂θ, 5h, 100%; q) 1.5eq. TBAF, THF, lh; r) 1.2 eq. PMBC1, 2eq. NaH, cat. n-BuNT, THF-DMF(5:1), 5h, 96% for 2 steps; s) Mel(xs), 5eq. NaH, THF-DMF(5:1), 12h, reflux, 93%; t) i, 80% AcOH, 12h; ii, 0.2eq. Mnθ₄, 4eq. NaI0₄, 0.5eq. Na₂C0₃, Dioxane-H₂θ(2.5:l), lOh, 95%

We begin with the route followed to reach 1. The starting material was the readily accessible 4, (7) obtained from the commercially available 2, -dimethoxy-3-methyl benzaldehyde . Compound 4 was converted by O-alkylation, as shown to ether 5. Dakin-like (8) oxidative cleavage of the aryl aldehyde linkage generated a formate, which was de-acylated by trans esterification. Protection of the resultant phenol afforded 6. The allylic ether had served to protect the C2 hydroxyl group while the substituent at CI was being adjusted in a constructive way. At this point, p-Claisen rearrangement and sequential protection of the phenol and primary allylic alcohol functions, as indicated, led to 7 and thence 8. Cleavage of the MOM group was now readily accomplished and the resultant phenol function was exploited to bring about O-hydroxymethylation (see compound 9) . Selective methylation of the phenolic hydroxyl and silylation of the primary benzylic alcohol led to compound 10.

The setting was in place to introduce the L-amino acid

•5_: functionality. An allylic alcohol (compound 11) was exposed on cleavage of the pivaloate. Sharpless A.E.,(6a) under the conditions shown, led to 12 in high e.e. (>95%) . Azidolysis of the oxirane linkage under titanium mediated direction (6c) afforded a diol 13. To allow for building the required N-methyl 0 ^tBoc linkage, the diol was protected as its acetonide (see structure 14) . From that point, the azide linkage was reductively cleaved in the presence of Boc anhydride to afford

16. Subsequent to cleavage of the TBS group and installation of a p-methoxybenzyl function, 16 was in hand. Following 5 N-methylation, hydrolysis of the acetonide, and oxidative cleavage of the diol, (9) compound 1 was secured.

Scheme 2. a) 1.6eq. Ph₃P=CH₂Li, THF, 0°C, lh, 96%; b) l.leq. AD-mix-α, t-BuOH-H₂0(l: l), 0°C, 3d, 99%; c) l.leq. TsCl, pyridine-CH₂Cl₂(l:l), Id, 95%; d) 2eq. K₂C0₃, MeOH, 4h, 95%; e) 4eq. NaN₃, 15eq. LiC10₄, CH₃CN, 60°C, 5h, (2°:l^c-6.5:l); f) l.leq. BnBr, 5eq. NaH, cat. n-BuN^T, THF, 5h, 90% for 2 steps; g) H₂, Pd/C, EtOAc, 1.2eq. (Boc^O, 5h, 100%; h) TFA-CH₂C1₂(1:2), then NaHC0₃; i) 4eq. ₂C0₃, 5eq. BrCH₂CH(OEt)₂, CH₃CN, reflux, 3d, 80% for 2 steps; j) 12N HC1-THF(1:1), then NaOH, 88% (β-OH:α-OH=4:l).

0 Referring to scheme 2, the synthesis of 2, with the suitable S configuration at the future C13, commenced with the known and readily available benzaldehdye 17, (10) which was converted to 18. Asymmetric di-hydroxylation (6b) of the styrene like double bond through the action of AD mix-a gave rise to 19 (> 95% e.e.), from which the epoxide 20 was derived as shown. 5 Azidolysis of the epoxide compound, under the conditions indicated, resulted in a 6.5:1 preference for attack at the benzylic, as opposed to primary carbon. The major product, 21, was converted to its O-benzyl derivative 22.

10 The azide linkage was reduced in the presence of Boc anhydride to afford 23. The 'Boc protection maneuver was conducted for convenience in the isolation process. Cleavage of the Boc group of 23 was followed by monoalkylation of the resultant amine function with diethylbromoacetal in high yield (see compound

15 24) . Finally, the tetrahydroisoquinole ring was produced by the Pomerantz-Fritsch type cyclization of 24. (11) Product 2 was obtained as a 4:1 mixture of β,α stereoisomers at the future C . As will be seen, this stereochemical issue is without consequence, since this center is destined to become a ketone 20 in short order.

Example 1 shows that a suitably directed p-Claisen rearrangement followed by Sharpless A.E. (6a) can be used to generate a significantly functionalized tyrosine (see compound 16)

25 analogue. Furthermore, Sharpless A.D., (6b) followed in due course by a modified Pomerantz-Fritsch cyclization, has been used to reach a valuable heavily functionalized tetrahydroisoquinoline subtype 2 in high e.e. Thus, the major subunits needed to reach the targets have been assembled by

30 chemistry, which included p-Claisen rearrangement, asymmetric epoxidation and asymmetric dihydroxylation. Example 2

Construction of Two Additional Chiral Subunits For Use in Preparation of the Saframycin-Ecteinascidin Series The following Schemes 3 and 4 resulted In two additional subunits, 3 and 4, respectively, which were used to prepare analogues within Saframycin-Ecteinascidin Series.

Scheme 3. a) MOMC1, i-Pr₂NEt, CH₂C1₂; b) Br'^ ^ -OTBS, K₂C0₃, CH₃CN, reflux; c) PhNMe,, Toluene, 210°C, 60% for 3 steps; d) Mel, K.₂Cθ₃,CH₃CN; e) TBAF, THF; f) PivCl, Pyridine, CH₂C1₂, 91% for 3steps; g) 3N HC1, THF-iPiOH; h)

Et₂AlCl, (CH₂θ)_n, CH₃C1₂, 84% for 2 steps; i) t-Bu₂Si(OTi)₂, 2,6-Lutidine,CHCl₃;j) DIBA -H, CH,C1₂, -78°C, 89% for 2 steps; k) SAE, 97%, >9^_5% ee; 1) Ti(θiPr)₂(N₃)₂, Benzene, reflux; m) DMP, Acetone, p-TsOH, 88% for 3 steps; n) (Boc^O, H₂, Pd/C, EtOAc; o) Mel, NaH, THF-DMF, reflux, 95% for 2 steps; p) TBAF, THF; q) BnBr, K.₂Cθ₃, nBu^NT, CHC13, MeOH; r) PMBC1, NaH, nBu₄N^"T, THF, DMF, 75% for 3 steps; s) 80% AcOH, then KMnθ₄, Nalθ₃, Na₂Cθ₃, Dioxane-H₂θ, 94% for 3 steps

Example 3

A Novel Face Specific Mannich Closure Providing Access to the Saframycin-Ecteinascidin Series of Piperazine Based Alkaloids

Continuing from Example 1, the following uses the building blocks of Example 1 to reach the saframycin-ecteinascidin series.

The anti backbone relationship between C3 and Cll in III, produced from 3, required a stereochemical correction to reach the syn series of quinocarcinol VI. Such a C3 - Cll syn relationship also pertains in I and II. We set as our goal compound III. In doing so, we would be revisiting the question of the reasons for the outcome of the backbone stereochemistry in the Mannich closure sequence.

Referring to Scheme 5 below, coupling of 1 and 2 via amide bond formation was accomplished through the action of BOPCl, (12) as shown, in 60 - 65% yield. Oxidation of the diastereomeric alcohol functions gave rise to 38 (75 - 80%) , as a homochiral entity. To set the stage for the envisaged annulation, it was necessary to expose the aryl aldehyde function from its protected benzyl alcohol precursor. Following deprotection and oxidation, the homochiral 39, bearing the strategic aldehyde, was in hand. However, attempts to reach 6 by means of a 3-point-attachment of a formic acid equivalent were unsuccessful. Only wit aromatic aldehyde in place was the cyclization realized.

In the event, exposure of compound 39 to the action of formic acid accomplished cleavage of the 'Boc group, thereby triggering Mannich-like double closure to produce 40 (which is also III) (75%) and 41 (17%). These products differ only in the "solvolytic" state of the primary center. In a subsequent step, 40 was converted to 41. Characterization of 40 and 41 by extensive NMR measurements (including COSY, ROESY, HMQC and HMBC techniques) established an unexpected and most welcome result. Not only had cyclization occurred, but also the piperazinone ring had been elaborated with the syn C3-C11 backbone stereochemical relationship required for I and II. The stereochemistry assigned to 40 (III) and 41 was verified by a crystallographic determination at a later stage of the synthetic sequence.

Scheme 5. a) l.leq. BOPCl, 2.5eq. Et₃N, CH Cl₂, lOh, 63%; b) 1.5eq. Dess-Maπin periodinate, CH₂Cl₂, 30min, 78%; c) 1.5eq. DDQ, CH₂Cl₂-buffer7.0-H₂CK20:l :1), 3h, 84%; d) 2eq. NMO. cat. TPAP. m.s. 4A, CH₂Cl₂, 30min, 84%; e) formic acid, reflux, lOh, 75% for 40, 17% for 41, 0 formic acid, reflux; g) H₂, Pd/C, EtOAc, 5h, >50%; h) NaHC0₃, MeOH, >50%; i) BBr₃, CH₂C1₂, 78°C, -80%; j) NaBH₄, MeOH, 0°C, -50%; ) CSA, Toluene, reflux, 62% for 49; 1) AIH₃, THF, 0°C -> r.t., -70%. Exaxnple 4

Synthesis of analogue 55 within the Saframycin-Ecteinascidin Series - Scheme 6

Scheme 6. a) Acθ₂, Pyridine, CH₂C1₂, -70% for 50; or TBSCl, Imidazole, DMAP (CaL), -70% for 51; b) PivCl Pyridine, CH₂C1₂, -60%; c) NaBR,, MeOH, 0°C, -50%; d) Dess-Martin periodinate, CH₂C1₂, -70% Example 5

Synthesis of analogue 63 within the Saframycin-Ecteinascidin Series using subunits 1 and 4 - Scheme 7

^•58 59 g .

62 (β-OH)

Scheme 7. a) l.leq. BOPCl, 2.5eq. Et₃N, CH₂C1 , 10h; b) 1.5eq. Dess-Martin periodinate, CH₂CI₂, 30min, -46% for 2 steps; c) 1.5eq. DDQ, CH₂Cl₂-buffer7.0-H₂O(20:l:l), 3h, 80%; d) 2eq. NMO, cat. TPAP, m.s. 4A, CH₂Cl₂, 30min, 80%; e) formic acid, reflux, lh, 60-70%; f) H₂, Pd/C, EtOAc, 5h; g) BBr₃, CH₂Cl₂, -78°C; h) NaBH₄, MeOH, 0°C; i) CSA Toluene, reflux. Example 6

Synthesis of analogues within the Saframycin-Ecteinascidin Series using subunits 3 and 4 - Scheme 8

Scheme 8. a) l.leq. BOPCl, 2.5eq. Et₃N, CH₂Cl₂, lOh; b) 1.5eq. Dess-Martin periodinate, CH₂C1₂, 30min, -48% for 2 steps; c) 1.5eq. DDQ, CH₂Cl₂-buffer7.0-H₂θ(20:l:l), 3h, 80%; d) 2eq. NMO, cat. TPAP, m.s. 4A, CH₂Cl₂, 30min, 80%; e) formic acid, reflux, lh, 60-70%, (66:67=~5:1); f) H₂, Pd C, EtOAc, 5h, >90%; g) BBr₃, CH₂Cl₂, -78°C; h) NaBH , MeOH, 0°C; i) CSA, Toluene, reflux. Example 7

Synthesis of analogues within the Saframycin-Ecteinascidin Series using subunits 3 and 2 - Scheme 9

^•77 ^♦78

Scheme 9. a) l.leq. BOPCl, 2.5eq. Et₃N, CH₂Cl₂, 10h; b 1.5eq. Dess-Martin periodinate, CH₂Cl₂, 30min, -50% for 2 steps; c) 1.5eq. DDQ, CH₂Cl₂-buffer7.0-H₂O (20:1:1), 3h, 70-80%; d) 2eq. NMO, cat TPAP, m.s. 4 A, CH₂C1₂, 30min, 70-80%; e) formic acid, reflux, lh, 60-70% (75:76=5:1); H₂, Pd C, EtOAc, 5h; g) BBr₃, CH₂C1₂, -78°C 93-99%; h) NaBH^ MeOH, 0°C, 50%; i) CSA, Toluene, reflux, 92%. Exanrple 8

Synthesis of analogues within the Saframycin-Ecteinascidin Series - Scheme 10

^•87

Scheme 10. a) 80% AcOH, lOh, then Mnθ₄, NaI0₄, Na₂C0₃, Dioxane, H₂0, >90%; b) i. l.leq. BOPCl, 2.5eq. Et₃N, CH₂C1₂, lOh; ii. Dess-Martin periodinate, CH₂C1₂, 60% for 2 steps; c) HF Py, THF, AcOH (Cat.), 93%; d) Mnθ₂, acetone, 72%; e) formic acid, reflux, lh, 60-70%; Br₂ or NBS, CC1₄, -60%; g) Ac₂θ, Pyridine, CH₂C1₂, -70%, (87:85=1 : 1); h) H₂, Pd/C, EtOAc. Example 9

Synthesis of analogues within the Saframycin-Ecteinascidin Series - Scheme 11

2

•93 94

Scheme 11. a) TBAF, THF, >90%; b) Mel, K₂C0₃, CHC1₃, MeOH, reflux, 80%; c) PMBC1, NaH, nBuNT, THF, DMF, 90%; d)

80% AcOH, lOh, then KMnθ₄, Nalθ₄, Na₂Cθ₃, Dioxane, H₂θ, 90% for 2 steps; e) l.leq. BOPCl, 2.5eq. Et₃N, CH₂C1₂, lOh; f) Dess-Martin periodinate, C Cl^ -50% for 2 steps; g) DDQ, CH₂C1₂, H₂0, Buffer 7.0, 85%; h) NMO, TPAP, 4A ms, CH₂CK 70%; i) formic acid, reflux, 1 h, 60-70%; j) H₂, Pd C, EtOAc. Mass Spectroscopy and ¹H-NMR Data for Selected Compounds

The following table provides the -NMR and MS data for selected compounds which are useful as cytotoxic agents:

Η NMR (CDC1₃, 500 MHz) 7.24-7.10 (m, 5H), 6.14 (t, J = 3.4 Hz, 1H), 5.08 (d, J = 3.6 Hz, 1H), 4.66 (d, J = 3.1 Hz, 1H), 4.52 (d, J = 12.2 Hz, 1H), 4.32 (d, J = 12.2 Hz, 1H), 4.0-3.5 (m, 3H), 3.88 (m, 1H), 3.80 (s, 3H), 3.77 (s, 3H), 3.76 (s, 3H), 3,67 (s, 3H), 3.55 (s, 3H), 3.54 (s, 3H), 3.01 (m, 2H), 2.51 (s, 3H), 2.03 (s, 6H); HRMS (FAB +) m/z calcd for C₃₆H₄₂θ₉N₂K 658.2527, found 658.2557.

Η NMR (CDC1₃, 500 MHz) 7.93 (s, 1H), 6.24 (dd, J = 6.2 Hz, 3.3 Hz, 1H), 5.02 (d, J = 3.6 Hz, 1H), 4.65 (d, J = 2.8 Hz, 1H), 4.38 (dd, J = 11.5 Hz, 6.4 Hz, 1H), 4.29 (d, J = 1 1.6 Hz, 2.6 Hz, 1H), 3.79 (s, 3H), 3.78 (s, 3H), 3.76 (s, 3H), 3.72 (m, 1H), 3.66 (s, 3H), 3.62 (s, 3H), 3.02-2.90 (m, 2H), 2.52 (s, 3H), 2.02 (s, 3H), 2.01 (s, 3H);

HRMS (FAB +) m/z calcd for C₃₀H₃₆O_l0N₂K 623.2007, found 623.2008.

41

(CDC1₃, 500 MHz) 6.08 (dd, J = 7.7 Hz, 4.4 Hz, 1H), 5.03 (d, J - 3.5 Hz, (d, J = 2.0 Hz, 1H), 4.0-3.5 (m, 3H), 3.80 (s, 3H), 3.79 (s, 3H), 3.77 (s, (m, 1H), 3.54 (s, 3H), 2.95 (m, 2H), 2.56 (s, 3H), 2.07 (s, 6H). MS(ESI+)

42

Η NMR (CDC1₃, 500 MHz) 10.99 (s, 1H), 5.94 (t, J = 3.9 Hz, lH), 5.12 (d, J - 3.0 Hz, 1H), 4.67 (s, 1H), 3.88 (m, 1H), 3.8-3.5 (m, 2H), 3.78 (s, 3H), 3.71 (s, 3H), 3.68 (s, 3H), 3.55 (s, 3H), 3.45 (s, 3H), 3.00 (m, 2H), 2.58 (s, 3H), 2.02 (s, 3H), 1.98 (s, 3H); MS(ESI +) m/z 543.6.

2

Η NMR (CDC1₃, 500 MHz) 7 30-7 15 (m, 5H) . 5 08 (s, IH), 445 (s, 2H), 4 26 (m, 2H), 3 90-3 70 (mjϋ), 3 85 (s, 3H), 3 71 (s, 3H), 3 63 (s, 6H), 3 61 (s, 3H), 3 583 (s, 3H), 3 577 (s, 3H), 3 56 (m, IH), 3 54 (d, J = 102 Hz, IH), 3 35 (br s,

lH), 3 24 (d, J = 124 Hz, 1H), 3 15 (br s, IH), 3 00 (dd, J = 18 3 Hz, 8 3 Hz,

48 IH), 2 78 (d, J = 18 4 Hz, IH), 220 (s, 3H), 2 15 (s, 6H), MS(ESI +) m/z 635 3

49

4 63 6 Hz 1 H) ) 1 92

Η NMR (CDCl_j, 400 MHz) 5 92 (s, IH), 5 10 (s, IH), 4 63 (s, IH), 4 08 (m, IH) 3 89 (m, IH), 3 81 (s, 3H), 3 76 (s, 3H), 3 75 (s, 3H), 3 66 (m, IH), 3 51 (s, 3H), 3 44 (s, 3H), 2 97 ( , 2H), 2 54 (s, 3H), 2 02 (s, 6H), MS(ESI +) m/z 670 8

SI

0 Hz, IH) 3 71 (s, 6H) 6 (s, 3H),

52 ,

4

Hz, 1 (m, , 3H), Hz, 1

667 4

),

76 17.3 Hz, IH), 2.38 (s, 3H), 2.19 (s, 3H), 2.17 (s, 3H); MS (ESI +) m/z 603.3.

5.77 (s, 3.81 d, J -

.3 (m, 17.4

78

2.11 (s,3H).

(s, IH), 6.29 (m, IH), 5.72 (s, H).4.09 (d, J = 11.5 Hz, 1 H), s, 3H), 2.14 (s, 3H); MS (ESI

86

Η NMR (CDCI₃, 500 MHz) 7.20-6.80 (m, 5H), 6.79 (s, IH), 6.28 (m, IH), 5.28 (s, lH),4.34(s, lH),4.20(m, lH),4.08(m, IH), 4.85-3.60 (m, 15H), 3.47 (m, IH), 3.15 (m, IH), 2.84 (d, J = 17.3 Hz, IH), 2.35 (s, 3H), 2.33 (s, 3H), 2.28 (s, 3H).

87

Η NMR (CDC1₃, 00 MHz) 7.20-6.80 (m, 5H), 6.63 (s, IH), 6.28 (t, J - 3.6 Hz, IH), 5.17 (s, IH), 4.46 (s, IH), 4.20-3.60 (m, 18H), 3.15 (m, IH), 2.80 (d, J - 17.3 Hz, IH), 2.38 (s, 3H), 2.21 (s, 3H), 2.18 (s, 3H); MS (ESI +) m/z 616.8.

93 Discussion

Referring to Scheme α, below, there is a strikingly different outcome in the seemingly similar ring closure steps of IV to V and 39 to 40 (or III) . We focus on the hypothetical

5 iminium ions VII and IX which presumably appear in the two progressions. In each case, the system has been programmed such that attack of the nucleophile can only occur from one face of the iminium el^'ectrophile (β-as drawn) . The interesting issue arises with respect to the stereochemistry

10 of the reaction of the nucleophile. If the enol is attacked from its α-face, the "anti" backbone will be produced ⁽cf. I^V to V₎ . Alternatively, attack from the β-face of the enol woul_d give rise to a syn backbone product (39 to 40⁾ .

IX Near planar amide Aside from issues of steric hindrance, there is a potentially important stereoelectronic consideration. In modeling the closure reaction, it is seen that the coplanarity of the amide substituents can be maintained only if the enol is attacked from its β-face. By contrast, attack at the α-face of the enol seems to require rotation about the amide in the direction of orthogonalization. From this perspective the syn backbone cyclization product would be expected (see stereostructure IX, which leads to 40 (or III) .

Comparable modeling reveals that in the case of hypothetical stereostructure VIII, which could also arise from IV, attack at the β-face of the enol, though favored from the perspective of maximal maintenance of amide coplanarity, would incur a serious steric interaction between ring B and the two carbon bridge. This hindrance would be compounded by a particularly close abutment between the β-disposed vinyl and carbomethoxy groups if cyclization leading to the hypothetical X were to ensue. Hence, V rather than X is produced. By contrast, in IX, where the 6-rnembered iminium ring contains two additional sp² centers, the steric problems arising from the emerging syn backbone bridged system are perhaps reduced. In summary, it is proposed that cyclization of 39 (by way of stereostructure IX) is governed by the stereoelectronic factor (maintenance of amide coplanarity) , while cyclization of IV (by way of stereostructure VII) , is dictated by an overriding steric hindrance effect, leads to V.

Subsequent studies revealed that the stereochemical outcome of the Mannich closure step is also a function of the substitution pattern on the aldehyde-containing aromatic ring that enters into the cyclization event. This shows that the Mannich-like closure of 39 to 40 (III₎ directly provides the backbone stereochemistry required for the subject alkaloids, in contrast to the stereochemical outcome in a related, earlier case (IV to V) .

Based on prior art, compounds which contain a two tetrahydroisoquinoline aromatic carbon nitrogen framework, such as saframycin B, saframycin A (13,14), saframycin S (15), ecteinascidin 729 (Et 729) (16) , Et 743 and Phthalascidin (3) have consistently exhibited pharmacological, antibiotic, cytotoxic, antitumor, anti-tumorigenic and cellular anti- proliferative activity both in vivo and in vi tro . Several publications reveal that compounds which possess a two tetrahydroisoquinoline aromatic carbon nitrogen framework can function as cytotoxic antitumor agents . (13, 14, 15 , 16, 3) Saframycins are also known for their antibiotic capabilities. (19) These cytotoxic antitumor agents have been shown to interact with DNA. (18,14) In similar core structured saframycins and ecteinacidins as the compounds of this invention, interactions occur between DNA and the core tetrahydroisoquinoline aromatic carbon nitrogen framework. (2,18,20) Compounds disclosed in this invention, based on chemical and structural similarities to pthalicidins, ecteinicidins and saframycins, are therefore capable of interacting with DNA as well as possessing antitumor, antibiotic, cytotoxic and cellular anti-proliferative activity both in vivo and in vi tro .

The pharmacological, antitumor, anti-tumorigenic, cytotoxic and cellular anti-proliferative activity of the compounds disclosed here both in vivo and in vitro can be determined by using published test procedures.

In vivo assays to determine a compound's antitumor capabilities are typically performed in rodents or other species. Tumor growth is determined by the growth of tumors from transplanted transformed cells or tumor xenographs into or onto the animal.

(See, eg., 13, 16, 21) In vitro assays to determine a compound's antitumor capabilities can be performed using a soft agar cloning assay to determine the in vitro effects of the disclosed compounds against primary tumor specimens taken directly from patients . (See, eg., 22) Anti-proliferative efficacy and cytotoxicity typically can be determined by absorbance of viable cells and the use of a reference wavelength to serve as an index for the viable cells . (See, eg., 3)

Exaπtple 10

Alternative construction of chiral subunits 3 and 4 for use in preparation of the Saframycin-Ecteinascidin Series. The following schemes 12 and 13 result in subunits, 3 and 4, which were used to prepare analogues within the Saframycin- Ecteinascidin Series.

^H

Scheme 12. a) TsCl, Et₃N, CH₂C1₂, 0°C, 2 h, 93%; b) IC1, AcOH, 70°C, 20 h, 92%; c) CH₃I, K₂C0₃, acetone, reflux, 12 h, 100%; d) NaOH, EtOH, H₂0, reflux, 4 h, 94%; e) (CH₂0)_n, Me₂AlCl, CH,C1₂, 0°C->rt, 12 h, 77%; BnBr, K₂C0₃, acetone, reflux, 12 h, 95%; g) PMBC1, NaH, n-Bu₄N⁴T, THF-DMF, it, 1~2 h, 99%; h) 28, (o-tolyl)₃P, Et₃N, Bu₄N"Cr, Pd(OAc)₂, DMF, 130^CC, 12 h, 78%; i) (S.SyEt-DuPhos, H₂ (100 psi), MeOH, it, 2 d, 90%; j) NaH, Mel, THF, 0°C- rt, 12 h,60%.

Scheme 13. (a) m-CPBA,/>-TsOH, CH₂C1₂; then Et₃N, CH₂Cl₂-MeOH, 100%; (b) Br₂, K₂C0₃, CH₂C1₂, -78°C, 80%; (c) A1C1₃, CH₂C1₂, rt, overnight, 99%; (d) BιCH₂Cl, Cs₂C0₃, MeCN, reflux, 82%; (e) Vinyltributyltin, Pd(PPh₃)₄₎ toluene, reflux, 90%; (f) AD-mix- , /-BuOH-H₂0(l :l), 0°C, 95%; (g) TsCl, pyridine-CH₂Cl₂; (h) K₂C0₃, MeOH, 72% for 2 steps; (i) NaN₃, LiC10₄, MeCN, 60°C; (j) BnBr.NaH, THF, 70% for 2 steps; (k) H₂, Pd/C, EtOAc, 90%; (1) K₂C0₃, BrCH₂CH(OEt)₂, MeCN, reflux, 72%; (m) 6N HC1, Dioxane, H₂0, then NaOH, 86% (β-OH:α-OH=2:3). Example 11

Synthesis of analogues within the Saframycin-Ecteinascidin Series using subunits 1 and 2 - Scheme 14.

46 104

^•45

Scheme 14. a) l.leq. BOPCl, 2.₅eq. Et₃N, CH₂C1₂, lOh, 63%; b) l.₅eq. Dess-Martin pcriodinane, CH₂C1₂, 30min, 78%; c) 1.5eq. DDQ, CH₂Cl₂-buffer7.0-H₂O(20:l:l), 3h, 84%; d) 2eq. NMO, cat. TPAP, m.s. 4A, CH₂C1₂, 30min, 84%; e) fomiic acid, reflux, lh, 70% f) BBr₃, CH₂C1₂, 78°C, 85%; g) NaBH₄, MeOH, 0°C, 70%; h) CSA Toluene, reflux, lh, 70% ; i) H₂, 10%Pd/C, EtOH-EtOAc, Conc.HCl, 140psi, 75-85°C, 80%; j) LiAlH,, MeOH; k) NaH, Mel, THF-DMF; 1) EtOH, NaBH^. Exaπrple 12

Synthesis of analogues within the Saframycin-Ecteinascidin Series using subunits 1 and 4 - Scheme 15

Scheme 15 a) l.leq BOPCl, 2 5eq Et₃N, CH₂C1₂, lOh, b) 1 5eq Dess-Martin pcπodmaiie, CH₂C1₂, 30mm, -46% for 2 steps; c) 1.5eq DDQ, CH₂Cl₂-bu fer7 0-H₂O(20 1 1), 3h, 80%, d) 2eq NMO, cat TPAP, m s 4A, CH₂C1₂, 30mιn, 80%, e) formic acid, reflux, lh, 60-70%, f) BBr₃, CH₂C1₂, -78°C, 90%, g) NaBR,, MeOH, 4h, 0^CC. 70%, h) CSA Toluene, reflux, lh, 60%, i) H₂, 10%Pd'C, cone HC1, EtOH-EtOAc, 14h, 75-85°C, 140psι Exarπple 13

Synthesis of analogues within the Saframycin-Ecteinascidin Series using subunits 3 and 4 - Scheme 16.

Scheme 16. a) l. leq. BOPCl, 2.5eq. Et₃N, CH₂C1₂, lOh; b) 1.5eq. Dess-Martin periodinane, CH₂C1₂, 30min, 83% for 2 steps; c) 1.5eq. DDQ, CH₂Cl₂-buffer7.0-H₂O{20:l: l), 3h, 87%; d) 2eq. NMO, cat. TPAP, m.s. 4A, CH₂C1₂, 30min, 94%; e) formic acid, reflux, lh, 60-70%; f) BBr₃, CH C1₂, -78°C, 0.5h, 92%; g) NaBH₄, MeOH, 0°C; h) CSA Toluene, reflux, lh, >80% 2 steps; i) H₂, 10%Pd/C, EtOH-EtOAc, lOOOpsi, 75-85°C, 15h, 80%. Example 14

Synthesis of analogues within the Saframycin-Ecteinascidin Series using subunits 3 and 4 - Scheme 17 ___..____

*75 78

79 81 113- *80

Scheme 17. a) l .leq. BOPCl, 2.5eq. Et₃N, CH₂C1₂, lOh; b) l.Seq. Dess-Martin periodinane, CH₂C1₂, 30min, -50% for 2 steps; c) 1.5eq. DDQ, CH₂Cl₂-buffer7.0-H₂O (20:1:1), 3h, 70-80%; d) 2eq. NMO, cat. TPAP, m.s. 4A, CH₂C1₂, 30min, 70-80%; e) formic acid, reflux, lh, 60-70%; f) BBr₃, CH₂C1₂, -78^CC 93-99%; g) NaBH , MeOH, 0°C, 50%; h) CSA, Toluene, reflux, 92%, i) H₂, 10%Pd C, EtOH-EtOAc, lOOOpsi, 75-85°C, 15h. REFΞKENCES

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5. For the previous work on the total syntheses of saframycins see: (a) T. Fukuyama, R. A. Sachleben, J. Am. Chem. Soc. 1982, 104, 4957. (b) T. Fukuyama, L. Yang. K. Ajeck, R. A. Sachleben, J. Am. Chem. Soc. 1990, 112, 3712. (c) A. Kubo, N. Saito, H. Nishioka, H. Yamato, K. Masubuchi, M. Nakamaura, J. Org. Chem. 1988, 53, 4295. A brilliant and ultimately concise total sytnhesis of the saframycins was disclosed by Professor Andrew Myers, Harvard University at the 1998 Tetrahedron Prize Symposium (216^cr' National Meeting of the American Chemical Society, Boston, MA, 1998) . A. G. Myers, D. W. Kung, J. Am. Chem. Soc. 1999, 121, 10828.

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13. Okumoto T, Kawana M, Nakamura I, Ikeda Y, Isagai K: Activity of safracins A and B, heterocyclic quinone antibiotics, on experimental tumors in mice, J An tibiot

(Tokyo) , vol. 38, No. 6, Jun 1985, pages 767-771

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15. Mikami Y, Yokoyama K, Tabeta H, Nakagaki K, Arai T: Saframycin S, a new saframycin group antibiotic, J Pharmacobiodyn . Vol. 4, No. 4, April 1981, pages 282-286

16. Reid JM, Walker DL, Ames MM. : Preclinical pharmacology of ecteinascidin 729, a marine natural product with potent antitu or activity Vol. 38, No. 4 (1996) pp 329-334

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Claims

What is claimed is

A compound having the formula :

wherein R_λ and R₄ is H, a C_x to C₄ alkyl group, or an acyl group; wherein R is an ether, ester, amide, aromatic group, a phthalimide group, a substituted phthalimide group or is covalently bound to R₆; wherein R_:, is =0, OH, an ether group, an acyl group, or a sulfide group; wherein R₅ is H, halogen, OH, -OC₍₂_₆₎ alkyl group, an ether group, an acyl group, or an amide group; wherein R₆ is =0, OH, 0CH₃, CN, an acyloxy group or is covalently bound to R₂; wherein R₇, is H, =0, OH, 0CH₃, halogen, an ether group, or an acyl group; wherein R₈ and R₉ are independently H, CH₃ , 0CH₃, OC₂H₅, Br, F, CF₃, or R₈ and R₉ are joined together as a methylenedioxy group, or other five or six membered ring; wherein R₁₀ and R_u are independently CH₃, 0CH₃, OC₂H₅, SCH₃, or SC₂H₅; wherein R₁₂ is H, a C_λ to C₄ alkyl group, or an acyl group; and wherein the chiral center marked * has the R or the S configuration.

The compound of claim 1, having the formula:

wherein R_{l r} R₂, R₃, R₄ , R₅, R₆, R₇ , R₈ , and R₉ are defined as aim 1.

3. The compound of claim 2, having the formula:

wherein R_{l r} R₂, R₃, R₄ , R₅, R₆, and R₇ are defined as in claim 1.

4. The compound of claim 3, wherein R_l is CH₃, R₃ is =0, R₄ is CH₃, R₅ is 0CH₃, R₆ is =0, and R_η is H.

5. The compound of claim 4, wherein R₂ is 0C(0)H.

6. The compound of claim 4, wherein R₂ is H.

7. The compound of claim 4, wherein R₂ is OH.

8. The compound of claim 4, wherein R₂ is -0-benzene.

9. The compound of claim 4, wherein R₂ is 0C0CH₃.

10. The compound of claim 4, wherein R₂ is -0-t- butyldimethylsilyl .

11. The compound of claim 4, wherein R, is -O-Pivaloyl

12. The compound of claim 3, wherein R_x is H, R₃ is =0, R₄ is CH₃, R₅ is 0CH₃, R₆ is =0, and R₇ is H.

13. The compound of claim 12, wherein R₂ is -O-pivaloyl.

14. The compound of claim 3, wherein R_x is H, R₃ is =0, R₄ is benzene₃, R₅ is 0CH₃, R₆ is =0, and R₇ is H.

15. The compound of claim 3, wherein R_x is H, R₃ is =0, R₄ is H, R₅ is 0CH₃, R₆ is =0, and R₇ is H.

16. The compound of claim 3, wherein R_x is H, R₃ is =0, R₄ is H, R₅ is H, R₆ is =0, and R₇ is H.

17. The compound of claim 3, wherein R₃ is =0, R₄ is H, R₅ is halogen, R₆ is =0, and R₇ is H.

The compound of claim 2, having the formula:

wherein R_{l r} R₂, R₃, R, R₅, R₆, and R₇ are defined as in claim 1.

19. The compound of claim 18, wherein R_x is CH₃, R₃ is =0, R is CH₃, R₅ is 0CH₃, R₆ is =0, and R₇ is H.

20. The compound of claim 19, wherein R₂ is OC(0)H.

21. The compound of claim 19, wherein R₂ is H.

22. The compound of claim 19, wherein R₂ is OH.

23. The compound of claim 19, wherein R₂ is -0-benzene.

24. The compound of claim 19, wherein R₂ is OC0CH₃.

25. The compound of claim 19, wherein R₂ is -0-t- butyldimethylsilyl .

26. The compound of claim 19, wherein R₂ is -0-Pivaloyl.

27. The compound of claim 18, wherein R is H, R₃ is =0, R₄ is CH₃, R₅ is OCH₃, R₆ is =0, and R₇ is H.

28. The compound of claim 27, wherein R₂ is -O-pivaloyl.

29. The compound of claim 18, wherein R_x is H, R₃ is =0, R₄ is benzene₃, R₅ is 0CH₃, R₆ is =0, and R₇ is H.

30. The compound of claim 18, wherein R_λ is H, R₃ is =0, R₄ is H, R₅ is 0CH₃, R₆ is =0, and R₇ is H.

31. The compound of claim 18, wherein Rj is H, R₃ is =0, R₄ is H, R₅ is H, R₆ is =0, and R₇ is H.

32. The compound of claim 18, wherein R_τ is H, R₃ is =0, R₄ is H, R₅ is halogen, R₆ is =0, and R₇ is H.

33. A compound having the formula:

wherein R_x and R₄ is H, a C_: to C₄ alkyl group, or an acyl group; wherein R₂ is an ether, ester, amide, an aromatic ring, a phthalimide group, a substituted phthalimide group or is covalently bound to R₆; wherein R₅ is H, halogen, OH, an ether group, an acyl group, or an amide group; wherein R₆ is =0, OH, 0CH₃, CN, or an acyloxy group or is covalently bound to R₂; wherein R₇, is =0, OH, halogen, an ether group, or an acyl group; wherein R₈ and R₉ are independently H, CH₃ , 0CH₃, OC₂H,, Br, F, CF₃, or R₈ and R₉ are joined together as a methylenedioxy group, or other five or six membered ring; wherein R₁₀ and R_u are independently CH₃, 0CH₃, OC₂H₅, SCH₃, or SC₂H₅; wherein R₁₂ is H, a C_x to C₄ alkyl group, or an acyl group.

4. The compound of claim 33, having the formula;

wherein R_{l f} R₂, R₄, R₅, R₆, R₇, R₈ and R₉ are defined as in claim 33 .

35. The compound of claim 34, having the formula:

wherein R_{l r} R₂, R₄, R₅, R₆, and R₇ are defined as in claim 33.

36. The compound of claim 35, wherein R_x is CH₃, R₄ is CH₃, R_L is OCH₃, R₆ is =0, and R₇ is H.

37. The compound of claim 36, wherein R₂ is 0C(0)H.

38. The compound of claim 36, wherein R₂ is H.

39. The compound of claim 36, wherein R₂ is OH.

40. The compound of claim 36, wherein R₂ is -0-benzene.

41. The compound of claim 36, wherein R₂ is 0C0CH₃.

42. The compound of claim 36, wherein R₂ is -O-t- butyldimethylsilyl .

43. The compound of claim 36, wherein R₂ is -O-Pivaloyl.

44. The compound of claim 35, wherein R_x is H, R₄ is CH₃, R₅ is 0CH₃, R₆ is =0, and R₇ is H.

45. The compound of claim 44, wherein R₂ is -0-pivaloyl .

46. The compound of claim 35, wherein R_: is H, R₄ is benzene₃, R₅ is OCH₃, R₆ is =0, and R₇ is H.

47. The compound of claim 35, wherein _λ is H, R₄ is H, R₅ is 0CH₃, R₆ is =0, and R₇ is H.

48. The compound of claim 35, wherein R₂ is H, R₄ is H, R₅ is H, R₆ is =0, and R₇ is H.

49. The compound of claim 35, wherein R_j is H, R₄ is H, R₅ is halogen, R₆ is =0, and R₇ is H.

50. The compound of claim 34, having the formula:

wherein R_lf R₂, R₄, R₅, R₆, and R₇ are defined as in claim 33.

51. The compound of claim 50, wherein R_λ is CH₃, R₄ is CH , R, is OCH₃, R₆ is =0, and R₇ is H.

52. The compound of claim 51, wherein R₂ is OC(0)H.

53. The compound of claim 51, wherein R₂ is H.

54. The compound of claim 51, wherein R₂ is OH.

55. The compound of claim 51, wherein R₂ is -O-benzene.

56. The compound of claim 51, wherein R₂ is OC0CH₃.

57. The compound of claim 51, wherein R₂ is -0-t- butyldimethylsilyl .

The compound of claim 51, wherein R₂ is -O-Pivaloyl

59. The compound of claim 50, wherein R₂ is H, R₄ is CH₃, R_s is OCH₃, R₆ is =0, and R₇ is H.

60. The compound of claim 59, wherein R₂ is -O-pivaloyl.

61. The compound of claim 50, wherein R_λ is H, R₄ is benzene₃, R₅ is 0CH₃, R₆ is =0, and R₇ is H.

62. The compound of claim 50, wherein R_x is H, R₄ is H, R₅ is 0CH₃, R_e is =0, and R₇ is H.

63. The compound of claim 50, wherein R_x is H, R₄ is H, R₅ is H, R₆ is =0, and R₇ is H.

64. The compound of claim 50, wherein R, is H, R₄ is H, R₅ is halogen, R₆ is =0, and R₇ is H.

65. A compound having the formula:

wherein R₄ is H, a C_x to C₄ alkyl group, or an acyl group; wherein R₅ is H, halogen, OH, an ether group, an acyl group, a sulfide group or an amide group; wherein R_n is CH₃, OCH₃, OC₂H₅, SCH₃, or SC₂H₅; and wherein R₁₂ is H, a C_x to C₄ alkyl group, or an acyl group.

66. A compound having the formula:

wherein R_: is H, a C_x to C₄ alkyl group, or an acyl group; wherein R₃ is =0, OH, an ether group, an acyl group, a sulfide group or an amide group; wherein R₈ and R₉ are independently H, CH₃, 0CH₃, O ,^ , SCH_j , SC₂H₅, or R₈ and R₉ are joined together to form a five or six membered ring; wherein R₁₀ is CH₃, OCH₃, OC₂H₅, SCH₃, or SC₂H₅.

67. A method of producing the compound of claim 1, comprising reacting a compound having the formula A as follows

with a compound having the formula B as follows

wherein R_x and R₄ is H, a C_x to C₄ alkyl group, or an acyl group; wherein R₃ is =0, OH, an ether group, an acyl group, a sulfide group or an amide group; wherein R₅ is H, halogen, OH, an ether group, an acyl group, a sulfide group or an amide group; wherein R₈ and R₉ are independently H, CH₃, 0CH₃, 0 11,, SCHj , SC₂H₅, or R₈ and R₉ are joined together to form a five or six membered ring; wherein R₁₀ and R_u are independently CH₃, 0CH₃, OC₂H₅, SCH₃, or SC₂H₅; and wherein R₁₂ is H, a C_x to C₄ alkyl group, or an acyl group, so as to produce the compound of claim 1.

68. The method of claim 67, wherein the reaction is performed in the presence of N,N-bis (2-oxo-3-oxazolidinyl) phosphinic chloride.

69. The method of claim 67, wherein the reaction is performed in the presence of Dess-Martin periodinate.

70. The method of claim 69, wherein the reaction is further performed in the presence of CH₂C1₂.

71. A method of producing the compound of claim 33, comprising reacting the compound of claim 1 with camphor sulfonic acid (CSA) in the presence of toluene.

72. A pharmaceutical composition for treating a tumor in a subject, comprising a pharmaceutically effective amount of the compound of claim 1 or 33 and a pharmaceutically acceptable carrier.

73. A method of inhibiting proliferation of tumor cells which comprises contacting the cells under suitable conditions with an effective amount of the compound of claim 1 or 33.

74. A method of treating a patient having a tumor characterized by proliferation of neoplastic cells which comprises administering to the patient an effective amount of the compound of claim 1 or 33.

75. The method of claim 74, wherein the effective amount is from about 0.5 mg to about 5 mg per day.

76. The method of claim 75, wherein the effective amount is from about 1 mg to about 3 mg per day.

77. The method of claim 76, wherein the effective amount is about 2 mg per day.

78. The compound of claim 65, having the formula:

wherein R₄ and R₅ are defined as in claim 65.

79. A compound as in claim 78, wherein R₄ is CH₃ and R₅ is CH₃

(compound 1) .

80. A compoumd as in claim 78, wherein R₄ is Bn and R₅ is H

(compound 3) .

81. The compound of claim 66 having the formula:

( Compound 2 ]

12. The compound of claim 66, having the formula:

wherein R_{l r} R₃, and R₁₀, are defined as in claim 66

83. The compound of claim 82, having the formula:

( Compound 4 )

84. A compound having the formula:

wherein R_λ and R₄ is H, a C_x to C₄ alkyl group, or an acyl group; . . wherein R₂ is an ether, ester, amide, aromatic group or is covalently bound to R₆; wherein R₃ is =0, OH, H, an ether group, an acyl group, or a sulfide group; wherein R₅ is H, halogen, OH, -OC₍₂.₆, alkyl group, an ether group, an acyl group, or an amide group; wherein R₆ is =0, OH, 0CH₃, CN, or an acyloxy group or is covalently bound to R₂; wherein R₇, is H, =0, OH, 0CH₃, halogen, an ether group, or an acyl group; wherein R₈ and R₉ are independently H, CH₃, 0CH₃, OC₂H₅, Br, F, CF₃, or R₈ and R₉ are joined together as a methylenedioxy group, or other five or six membered ring; wherein R^" ₁₀ and R_n are independently CH₃, 0CH₃, OC₂H₅, SCH₃, or SC₂H₅; wherein R₁₂ is H, a C_λ to C„ alkyl group, or an acyl group; and wherein the chiral center marked * has the R or the S configuration . The compound of claim 84, having the formula:

wherein R_x, R₂, R₃, R , R₅, R₆, R₇ , R₈ , and R₉ are defined as in claim 84.

86. The compound of claim 85, having the formula:

wherein R_{l r} R₂, R₃, R₄ , R₅ , Rg , and R₇ are defined as in claim 84

87. The compound of claim 86, wherein R_x is H, R₂ is OH, R₃ is H, R₄ is H, R₅ is H, R₆ is =0, and R₇ is H (Compound 113) .

88. The compound of claim 86, wherein R₃ is H, R₄ is CH₃, R₅ is 0CH₃, and R₇ is H.

89. The compound of claim 88, wherein R₂ is OH.

90. The compound of claim 89, wherein R₆ is H and R_x is CH₃ (Compound 107) .

91. The compound of claim 89, wherein R₆ is =0 and R_: is H (Compound 104) .

92. The compound of claim 88, wherein R₂ and R₆ are joined as an ester bond.

93. The compound of claim 92, wherein R_x is H (Compound 105).

94. The compound of claim 92, wherein R_x is CH₃ (Compound 106) .

95. The compound of claim 84, having the formula:

wherein R_{l r} R₂, R₃, R , R₅, Rg , and R₇ are defined as in claim 84.

96. The compound of claim 95, wherein R_x is H, R₂ is OH, R₆ is =0, and R₇ is H.

97. The compound of claim 96, wherein R₄ is CH₃, R₅ is OCH₃.

98. The compound of claim 97, wherein R₃ is OH (Compound 109) .

99. The compound of claim 97, wherein R₃ is H (Compound 111) .

100. The compound of claim 96, wherein R₃ is H, R₄ is H and R₅ is H (Compound 112) .

101. The compound of claim 95, wherein R_λ is H, R₂ is OH, R₃ is =0, R₄ is CH₃, R₅ is 0CH₃, R₆ is =0, and R₇ is H. (Compound 108) .

102. The compound of claim 50, wherein R_x is H, R₂ is OH, R₄ is CH₃, R₅ is CH₃, R₆ is =0, and R₇ is H (Compound 110) .

103. The method of claim 67, wherein the compound having formula B is:

104. A method of producing the compound of claim 84, comprising reacting a compound having the formula A as follows:

with a compound having the formula C as follows

wherein R_x and R₄ is H, a C_λ to C₄ alkyl group, or an acyl group; wherein R₃ is =0, OH, an ether group, an acyl group, a sulfide group, an amide group H; wherein R₅ is H, halogen, OH, an ether group, an acyl group, a sulfide group or an amide group; wherein R₈ and R₉ are independently H, CH₃, OCH₃ , 0C,I- , SCH; , SC₂H₅, or R₈ and R₉ are joined together to form a five or six membered ring; wherein R₁₀ and R_n are independently CH₃, 0CH₃, OC₂H₅, SCH₃, or SC₂H₅; and wherein R₁₂ is H, a C_x to C₄ alkyl group, or an acyl group, so as to produce the compound of claim 84.

105. The method of claim 104, wherein the compound having the formula C is:

106. The method of claim 104, wherein the reaction is performed in the presence of W,Z\J-bis (2-oxo-3-oxazolidinyl) phosphinic chloride .

107. The method of claim 104, wherein the reaction is performed in the presence of Dess-Martin periodinate.

108. The method of claim 107, wherein the reaction is further performed in the presence of CH₂C1₂.

109. The method of claim 104, wherein the reaction is performed in the presence of H₂, 10%Pd/C, Ethanol-ascetic acid and hydrochloric acid.

110. A method of producing the compound of claim 1, comprising reacting the compound of claim 33 with H₂, 10%Pd/C, Ethanol-ascetic acid in the presence of hydrochloric acid.

111. The compound of claim 33, wherein R₂ is an ether, ester, amide, an aromatic ring or is covalently bound to R₆.

112. A method of preparing the compound in claim 1, comprising reacting the compound in claim 111 with H₂, 10%Pd/C, Ethanol-ascetic acid in the presence of hydrochloric acid.

113. The compound of claim 50, wherein R, is an ether, ester, amide, an aromatic ring or is covalently bound to R₆.

114. A method of preparing the compound in claim 18, comprising reacting the compound in claim 113 with H₂, 10%Pd/C, Ethanol-ascetic acid in the presence of hydrochloric acid.

115. A pharmaceutical composition for treating a tumor in a subject, comprising a pharmaceutically effective amount of the compound of claim 84 or 95 and a pharmaceutically acceptable carrier.

116. A method of inhibiting proliferation of tumor cells which comprises contacting the cells under suitable conditions with an effective amount of the compound of claim 84 or 95.

117. A method of treating a patient having a tumor characterized by proliferation of neoplastic cells which comprises administering to the patient an effective amount of the compound of claim 84 or 95.

118. The method of claim 117, wherein the effective amount is from about 0.5 mg to about 5 mg per day.

119. The method of claim 118, wherein the effective amount is from about 1 mg to about 3 mg per day. The method of claim 119, wherein the effective amount is about 2 mg per day.