WO2004033442A2 - Novel taxanes and methods related to use and preparation thereof - Google Patents

Novel taxanes and methods related to use and preparation thereof Download PDF

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Publication number
WO2004033442A2
WO2004033442A2 PCT/CA2003/001521 CA0301521W WO2004033442A2 WO 2004033442 A2 WO2004033442 A2 WO 2004033442A2 CA 0301521 W CA0301521 W CA 0301521W WO 2004033442 A2 WO2004033442 A2 WO 2004033442A2
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Prior art keywords
compound
portion contains
hydroxyl
aryloxy
alkoxy
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PCT/CA2003/001521
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French (fr)
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WO2004033442A3 (en
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Ragina Naidu
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Chatham Biotec Ltd.
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Priority to EP03757580A priority Critical patent/EP1562927B1/en
Priority to CA2501805A priority patent/CA2501805C/en
Priority to AT03757580T priority patent/ATE431343T1/en
Priority to DE60327651T priority patent/DE60327651D1/en
Priority to JP2004542120A priority patent/JP2006513152A/en
Priority to AU2003273671A priority patent/AU2003273671A1/en
Publication of WO2004033442A2 publication Critical patent/WO2004033442A2/en
Publication of WO2004033442A3 publication Critical patent/WO2004033442A3/en

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C233/00—Carboxylic acid amides
    • C07C233/64—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings
    • C07C233/81—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups
    • C07C233/82—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom
    • C07C233/87—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom of a carbon skeleton containing six-membered aromatic rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
    • C07C323/50—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton
    • C07C323/51—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton
    • C07C323/57—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being further substituted by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C323/58—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being further substituted by nitrogen atoms, not being part of nitro or nitroso groups with amino groups bound to the carbon skeleton
    • C07C323/59—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being further substituted by nitrogen atoms, not being part of nitro or nitroso groups with amino groups bound to the carbon skeleton with acylated amino groups bound to the carbon skeleton
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D205/00—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom
    • C07D205/02—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings
    • C07D205/06—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D205/08—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with one oxygen atom directly attached in position 2, e.g. beta-lactams
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D305/00—Heterocyclic compounds containing four-membered rings having one oxygen atom as the only ring hetero atoms
    • C07D305/14—Heterocyclic compounds containing four-membered rings having one oxygen atom as the only ring hetero atoms condensed with carbocyclic rings or ring systems

Definitions

  • the present invention relates generally to taxanes, compounds useful in the preparation of taxanes, and synthetic methods useful in the preparation of taxanes.
  • paclitaxel which has the following structure
  • Paclitaxel was first isolated from the bark of the pacific yew tree (Taxus brevifolia) in 1971 , and has proved to be a potent natural anticancer agent. For example, paclitaxel has been found to have activity against different forms of leukemia and against solid tumors in the breast, ovary, brain, and lung in humans.
  • Taxotere has been found to have very good anti-tumor activity and better bio-availability than paclitaxel. Taxotere is similar in structure to paclitaxel, having t-butoxycarbonyl instead of benzoyl on the amino group at the 3' position, and a hydroxyl group instead of the acetoxy group at the C-10 position (see EP 253738 for a discussion of taxotere).
  • Taxanes are structurally complicated molecules, and the development of commercially viable synthetic methods to make taxanes has been a challenge. Semi-synthetic pathways have been developed, where these methods begin with the isolation of a naturally occurring material and then the conversion of that material to the taxane of interest. One such pathway for the semi-synthesis of paclitaxel begins with 10-deacetylbaccatin III, a taxane isolated from the needles of the English yew tree (Taxus baccata).
  • the present invention provides a process of preparing a beta-lactam, where the process comprises the scheme
  • Ri is hydroxyl, protected hydroxyl, thiol, or protected thiol; LG is a leaving group;
  • R 2 is alkyl, alkenyl, alkynyl, or aryl where R 2 is optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms; and R 3 is hydrogen.
  • Ri is phenyl and R 2 is phenyl.
  • the present invention provides a compound of the formula
  • R is thiol (SH), tBOC, acetate, methoxy, thiophenyl, CI 2 CH-C(O)O- or 1-ethoxyethyl, R 2 is phenyl and R 3 is hydrogen, and salts thereof.
  • the present invention provides a process of opening a beta-lactam ring, where the process comprises the scheme
  • Ri is hydroxyl, protected hydroxyl, thiol, or protected thiol; LG is a leaving group; PG is an amine protecting group; R 2 is alkyl, alkenyl, alkynyl, or aryl where R 2 is optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms; R 3 is hydrogen, Ci-C ⁇ alkyl or aryl where R 3 is optionally substituted with one or more halogens, hydroxyl, alkoxy, aryloxy, heteroaryloxy,
  • the present invention provides an isoserine compound of the formula
  • Ri is hydroxyl, protected hydroxyl, thiol, or protected thiol
  • PG is an amino protecting group
  • R 2 is alkyl, alkenyl, alkynyl, or aryl where R 2 is optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms;
  • R 3 is hydrogen, Ci-C ⁇ alkyl or aryl where R 3 is optionally substituted with one or more halogens, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alky
  • the present invention provides a process comprising the following scheme
  • An and Ar 2 are each aryl groups, where each of A ⁇ and Ar 2 is independently optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbon atoms, and aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon atoms;
  • X is halide;
  • R 5 is selected from hydrogen, benzoyl and tBOC, and M is a halogenating agent.
  • the present invention provides a compound of the formula
  • Ari and Ar 2 are each aryl groups, where each of An and Ar 2 are independently optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbon atoms, and aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon atoms;
  • X is halide; and R 5 is selected from hydrogen, benzoyl tBOC, C ⁇ -C 6 alkyl or aryl where R 5 is optionally substituted with one or more halogens, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano
  • the present invention provides a process comprising the scheme
  • An and Ar 2 are each aryl groups, where each of A ⁇ and Ar 2 are independently optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbon atoms, and aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon atoms; M is metal and X is one or more halides attached to the metal; R 5 is selected from hydrogen, benzoyl and tBOC; and Re is Ci-C ⁇ alkyl.
  • the present invention provides a compound of the formula
  • Ari and Ar 2 are each aryl groups, where each of Ari and Ar 2 are independently optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbon atoms, and aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon atoms;
  • R 5 is selected from hydrogen, benzoyl and tBOC; and
  • Rg is a hydroxyl protecting group.
  • Rg is selected from methoxymethyl, methoxyethyl, 1-ethoxyethyl, benzyloxymethyl, (beta-trimethylsilyl-ethoxy)methyl, tetrahydropyranyl, 2,2,2-trichloro- ethoxycarbonyl, benzyloxycarbonyl, tetf-butoxycarbonyl, 9- fluorenylmethoxycarbonyl, 2,2,2-trichloroethoxymethyl, trimethylsilyl, triethylsilyl, tripropylsilyl, dimethylethylsilyl, dimethyl(t-butyl)silyl, d iethy Imethy Isi ly I , dimethylphenylsilyl, diphenylmethylsilyl, acetyl, chloroacetyl, dichloroacetyl, trichloroacetyl and trifluoroacetyl.
  • R 5 is selected from hydrogen, benzoyl and tBOC
  • Re is a hydroxy protecting group
  • R is hydrogen or Ci-C ⁇ alkyl
  • H+ represents a proton source, e.g., an organic acid or mineral acid.
  • the present invention provides a process of opening a beta lactam according to the scheme
  • PG is a hydroxyl protecting group
  • a and Ar 2 are each aryl groups, where each of An and Ar 2 are independently optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbon atoms, and aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon atoms;
  • Ri is hydrogen, alkyl, or -O-PG wherein PG is a protecting group, and H+ represents a proton source, e.g., organic or mineral acid.
  • the present invention provides a compound of the formula
  • An and Ar 2 are each aryl groups, where each of An and Ar 2 is independently optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbon atoms, and aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon atoms; Re is selected from hydrogen, benzoyl and tBOC; R 6 is a hydroxyl protecting group, and R is hydrogen or C C 6 alkyl.
  • R 6 is selected from methoxymethyl, methoxyethyl, 1- ethoxyethyl, benzyloxymethyl, (beta-trimethylsilyl-ethoxy)methyl, tetrahydropyranyl, 2,2,2-trichloro-ethoxycarbonyl, benzyloxycarbonyl, tert- butoxycarbonyl, 9-fluorenylmethoxycarbonyl, 2,2,2-trichloroethoxymethyl, trimethylsilyl, triethylsilyl, tripropylsilyl, dimethylethylsilyl, dimethyl(t-butyl)silyl, diethylmethylsilyl, dimethylphenylsilyl, diphenylmethylsilyl, acetyl, chloroacetyl, dichloroacetyl, trichloroacetyl and trifluoroacetyl.
  • the present invention provides a process comprising the scheme
  • An and Ar 2 are each aryl groups, where each of An and Ar 2 is independently optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbon atoms, and aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon atoms;
  • R 5 is selected from hydrogen, benzoyl and tBOC,
  • R 6 is C ⁇ -C 6 alkyl
  • R 7 is H or C ⁇ -C 6 alkyl
  • E represents a desulfuration reagent.
  • the present invention provides a compound of the formula
  • Ar 2 is an aryl group optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbon atoms, and aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon atoms;
  • R 5 is selected from hydrogen, benzoyl and tBOC;
  • R 6 is a hydroxyl protecting group, and R 7 is H or C ⁇ -C 6 alkyl.
  • Optional hydroxyl protecting groups for Re include, without limitation, methoxymethyl, methoxyethyl, 1-ethoxyethyl, benzyloxymethyl, (beta- trimethylsilyl-ethoxy)methyl, tetrahydropyranyl, 2,2,2-trichloro-ethoxycarbonyl, benzyloxycarbonyl, te/f-butoxycarbonyl, 9-fluorenylmethoxycarbonyl, 2,2,2- trichloroethoxymethyl, trimethylsilyl, triethylsilyl, tripropylsilyl, dimethylethylsilyl, dimethyl(t-butyl)silyl, diethylmethylsilyl, dimethylphenylsilyl, diphenylmethylsilyl, acetyl, chloroacetyl, dichloroacetyl, trichloroacetyl and trifluoroacetyl.
  • the present invention provides a compound of the formula
  • Ar 2 is an aryl group optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbon atoms, and aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon atoms;
  • R 5 is selected from hydrogen, benzoyl and tBOC, R 6 is a thiol protecting group, and R 7 is H or C ⁇ - C 6 alkyl.
  • the present invention provides a process of substituting the nitrogen of a beta lactam, comprising treating a beta lactam of the structure
  • An and Ar 2 are each aryl groups, where each of An and Ar 2 is independently optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbon atoms, and aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon atoms; and R 5 is selected from benzoyl and tBOC.
  • the protecting agent is benzoyl chloride or di-tert-butyl- dicarbonate.
  • this process is preceeded by forming a beta lactam of the formula
  • the base is ammonia.
  • the present invention provides a process for preparing a beta lactam, comprising the scheme
  • Ri is hydroxyl, protected hydroxyl, thiol, or protected thiol; LG is a leaving group;
  • R 2 is alkyl, alkenyl, alkynyl or aryl, where R 2 may be optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms; and PG is a protecting group.
  • the present invention provides a compound of the formula
  • Ri is hydroxyl, protected hydroxyl, thiol, or protected thiol
  • R 2 is alkyl, alkenyl, alkynyl or aryl, where R 2 may be optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms; and PG is a protecting group.
  • the present invention provides a process comprising the scheme
  • Ri is hydroxyl, protected hydroxyl, thiol, or protected thiol
  • R 2 is alkyl, alkenyl, alkynyl or aryl, where R 2 may be optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms; and PG is a protecting group, where H+ represents a proton source such as organic or mineral acid.
  • the present invention provides a compound of the formula wherein Ri is hydroxyl, protected hydroxyl, thiol, protected thiol, alkyl, alkenyl, alkynyl, or aryl where Ri is optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms; R 2 is alkyl, alkenyl, alkynyl or aryl, where R 2 may be optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy,
  • Ri is selected from methoxymethyl, methoxyethyl, 1-ethoxyethyl, benzyloxymethyl, (beta-trimethylsilyl- ethoxy)methyl, tetrahydropyranyl, 2,2,2-trichloro-ethoxycarbonyl, benzyloxycarbonyl, te/f-butoxycarbonyl, 9-fluorenylmethoxycarbonyl, 2,2,2- trichloroethoxymethyl, trimethylsilyl, triethylsilyl, tripropylsilyl, dimethylethylsilyl, dimethyl(t-butyl)silyl, diethylmethylsilyl, dimethylphenylsilyl, diphenylmethylsilyl, acetyl, chloroacetyl, dichloroacetyl, trichloroacetyl and trifluoroacetyl.
  • the present invention provides a process of replacing a thioaryl group with a hydroxyl group according to the scheme
  • PG is an amine protecting group
  • An and Ar 2 are each aryl groups, where each of An and Ar 2 is independently optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbon atoms, and aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon atoms; E is hydrogen or an organic group, and Hg represents a mercury-containing oxidizing agent.
  • PG is benzoyl or tBOC; optionally, E is hydrogen; optionally, An and Ar 2 are each phenyl; and optionally Hg is HgO or Hg(CF 3 CO 2 ) 2 .
  • the present invention provides a process of replacing a thioaryl group with a hydroxyl group according to the following scheme
  • Hg represents a mercuric reagent
  • An and Ar 2 are independently selected from alkyl, alkenyl, alkynyl, aryl or substituted aryl radical
  • R-io is hydrogen, C-i-C ⁇ alkyl, aryl or substituted aryl radical
  • a substituted aryl radical is substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms.
  • Exemplary mercuric reagents are mercuric oxide and mercuric trifluoroacetate.
  • the present invention provides a process comprising esterifying a compound of the formula
  • Re is acetyl or dichloroacetyl; and R 7 is triethylsilyl, dichloroacetyl or 2,2,2-trichloroethoxycarbonyl (Troc); with an acid compound of a formula selected from
  • the acid compound has the formula
  • An is phenyl and Rg is thiophenyl, acetoxy, methoxy, t-butoxycarbonyloxy, phenoxy, ethoxyethyl, or dichloroacetyl.
  • the acid compound has the formula
  • An is phenyl
  • R 8 is hydrogen or PMP
  • R 9 is acetoxy, methoxy, t-butoxycarbonyloxy, phenoxy, ethoxyethyl, or dichloroacetyl.
  • the present invention provides a compound of the formula
  • Re and R are independently selected from hydrogen, triethylsilyl, acetyl and dichloroacetyl, with the proviso that Re and R 7 may not be simultaneously hydrogen, R 8 is tBOC, PMP, Bz or H, and Rg is thiophenyl, acetoxy, methoxy, t-butoxycarbonyloxy, ethoxyethyl, or dichloroacetyl.
  • R & and R are each dichloroacetyl; Rs is tBOC; and Rg is thiophenyl, acetoxy, methoxy, t-butoxycarbonyloxy, ethoxyethyl, or dichloroacetyl.
  • R 6 is acetyl
  • R 7 is -TES
  • R 8 is t-BOC
  • Rg is thiophenyl, acetoxy, methoxy, t-butoxycarbonyloxy, or dichloroacetoxy.
  • R 6 and R 7 are each dichloroacetyl, R 8 is tBOC, PMP or H, and Rg is acetoxy.
  • R 6 is acetyl
  • R 7 is triethylsilyl
  • R 8 is tBOC
  • the present invention provides a process comprising the scheme wherein R 6 and R are independently selected from hydrogen, triethylsilyl, acetyl and dichloroacetyl, with the proviso that Re and R 7 may not be simultaneously hydrogen, R 8 is tBOC, PMP, Bz or H, and Rg is thiophenyl, acetoxy, methoxy, t-butoxycarbonyloxy, ethoxyethyl, or dichloroacetyl.
  • the compound of structure (I) is deprotected at the 2' position to form an intermediate of structure (la), and the intermediate is treated with zinc acetate dihydrate to form the compound of formula (II), where the intermediate has the structure
  • the compound of formula (I) is treated with protic acid and tertiary amine in an organic solvent to form an intermediate of formula (lb), and the intermediate is deprotected at the 2' position to form the compound of formula (II), where the intermediate has the structure
  • the present invention provides a method of preparing TAXOTERE, comprising reacting a compound of structure (III) with t- BOC, followed by deprotection of at least one of the 2', 7 and 10 positions, where the compound of structure (III) is
  • Re and R 7 are independently selected from hydrogen, triethylsilyl, acetyl, Troc and dichloroacetyl, with the proviso that Re and R 7 may not be simultaneously hydrogen, and R 9 is thiophenyl, acetoxy, methoxy, t-butoxycarbonyloxy, or dichloroacetyl or ethoxyethyl.
  • R 6 and R are each dichloroacetyl and Rg is acetoxy.
  • the compound of structure (III) is prepared by the reduction of a compound of structure (IV)
  • Re and R are each dichloroacetyl, Rg is acetoxy, and Rn is OCO-t-Bu.
  • R 6 is acetyl or dichloroacetyl
  • R 7 is TES or Troc
  • Rg is acetoxy or ethoxyethyl.
  • the compound of structure (III) is prepared by the reduction of a compound of structure (IV)
  • R 6 is Ac
  • R 7 is TES
  • Rg is acetoxy
  • Rn is PMP, OCOO-t-Bu or H.
  • the present invention provides a process comprising the scheme
  • An and Ar 2 are independently selected from alkyl, alkenyl, alkynyl, aryl or substituted aryl radical; and R 10 is hydrogen, C ⁇ -C 6 alkyl, aryl or substituted aryl radical; where a substituted aryl radical is substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms.
  • the wavy line from AnS to the ring indicates that both the alpha and beta forms are included.
  • the present invention provides a process of coupling a beta lactam to a baccatin III compound according to the following scheme
  • R 3 and R are independently selected from hydrogen, hydroxyl, protected hydroxyl, thiol, protected thiol, alkyl, alkenyl, alkynyl, or aryl where R 3 and R 4 are optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms; R 7 is hydroxyl or a protected hydroxyl group; and the coupling is performed by addition of metal hydride, metal alkoxide or lewis acid to the reaction mixture.
  • the present invention provides a process for making a compound of formulas (III 1 ) or (IV):
  • Figure 1 illustrates several chemical routes for the preparation of beta-lactam and phenylisoserine sidechains according to the present invention.
  • Figure 2 illustrates a chemical route for the preparation of beta- lactam and phenylisoserine sidechains according to the present invention.
  • Figure 3 illustrates a chemical route for the preparation of a beta- lactam and phenylisoserine sidechain according to the present invention.
  • Figure 4 illustrates chemical routes for the preparation of taxotere from various intermediate compounds prepared according to the present invention.
  • Figure 5 illustrates chemical routes for the preparation of taxotere from various intermediate compound prepared according to the present invention.
  • the present invention relates to 3-phenylisoserine compounds as well as the preparation thereof and the intermediates formed during their preparation; baccatin III compounds and the preparation thereof; methods of joining together a 3-phenylisoserine compound and a baccatin III compound as well as the resulting chemical structure(s); and the conversion of one taxane compound to another taxane compound as well as the resulting chemical structure(s).
  • hydroxy-protecting group refers to a readily cleavable group bonded to the oxygen of a hydroxyl (-OH) group.
  • hydroxy protecting groups include, without limitation, acetyl (Ac), benzyl (PhCH 2 ), 1- ethoxyethyl (EE), methoxymethyl (MOM), (methoxyethoxy)methyl (MEM), (p- methoxyphenyl)methoxymethyl (MPM), tert-b uty Id i methy Isi ly I (TBS), tert- butyldiphenylsilyl (TBPS), tert-butoxycarbonyl (tBoc, t-Boc, tBOC, t-BOC), tetrahydropyranyl (THP), triphenylmethyl (Trityl, Tr), 2-methoxy-2-methylpropyl, benzyloxycarbonyl (Cbz), trichlor
  • protected hydroxy group refers to a hydroxy group that is bonded to a hydroxy-protecting group.
  • protected hydroxy groups include, without limitation, -O-alkyl, -O-acyl, acetal, and -O-ethoxyethyl, where some specific protected hydroxy groups include, formyloxy, acetoxy, propionyloxy, chloroacetoxy, bromoacetoxy, dichloroacetoxy, trichloroacetoxy, trifluoroacetoxy, methoxyacetoxy, phenoxyacetoxy, benzoyloxy, benzoylformoxy, p-nitro benzoyloxy, ethoxycarbonyloxy, methoxycarbonyloxy, propoxycarbonyloxy, 2,2,2-trichloro ethoxycarbonyloxy, benzyloxycarbonyloxy, tert.-butoxycarbonyloxy, 1 -cyclopropyl ethoxycarbonyloxy,
  • Hydroxy protecting groups and protected hydroxy groups are described in, e.g., C. B. Reese and E. Haslam, "Protective Groups in Organic Chemistry,” J. G. W. McOmie, Ed., Plenum Press, New York, N.Y., 1973, Chapters 3 and 4, respectively, and T. W. Greene and P. G. M. Wuts, "Protective Groups in Organic Synthesis,” Second Edition, John Wiley and Sons, New York, N.Y., 1991 , Chapters 2 and 3.
  • thiol-protecting group refers to a readily cleavable group bonded to the sulfur of a thiol (-SH) group.
  • thiol protecting groups include, without limitation, triphenylmethyl (trityl, Trt), acetamidomethyl (Acm), benzamidomethyl, 1 -ethoxyethyl, benzoyl, and the like.
  • the related term "protected thiol group” refers to a thiol group that is bonded to a thiol- protecting group.
  • protected thiol groups include, without limitation, -S-alkyl (alkylthio, e.g., C ⁇ -C ⁇ oalkylthio), -S-acyl (acylthio), thioacetal, -S-aralkyl (aralkylthio, e.g., aryl(C ⁇ -C 4 )alkylthio), where some specific protected thiols groups include methylthio, ethylthio, propylthio, isopropylthio, butylthio, isobutylthio, sec-butylthio, tert-butylthio, pentylthio, isopentylthio, neopentylthio, hexylthio, heptylthio, nonylthio, cyclobutylthio, cyclopentylthio and cyclohexylthio, benzylthio,
  • Thio protecting groups and protected thio groups are described in, e.g., C. B. Reese and E. Haslam, "Protective Groups in Organic Chemistry,” J. G. W. McOmie, Ed., Plenum Press, New York, N.Y., 1973, Chapters 3 and 4, respectively, and T. W. Greene and P. G. M. Wuts, "Protective Groups in Organic Synthesis,” Second Edition, John Wiley and Sons, New York, N.Y., 1991 , Chapters 2 and 3.
  • amine protecting group refers to groups known in the art that can be used to protect an amine group from undergoing an undesired chemical reaction.
  • examples of amine protecting groups include, but are not limited to: acyl types such as formyl, trifluoroacetyl, phthalyl, and p- toluenesulfonyl; aromatic carbamate types such as benzyloxycarbonyl (Cbz) and substituted benzyloxy-carbonyls, 1-(p-biphenyl)-1-methylethoxy-carbonyl, and 9-fluorenylmethyloxycarbonyl (Fmoc); aliphatic carbamate types such as tert-butyloxycarbonyl (tBoc), ethoxycarbonyl, diisopropylmethoxycarbonyl, and allyloxycarbonyl; cyclic alkyl carbamate types such as cyclopentyloxycarbonyl and adamantyloxycarbonyl;
  • Amine protecting groups and protected amine groups are described in, e.g., C. B. Reese and E. Haslam, "Protective Groups in Organic Chemistry,” J. G. W. McOmie, Ed., Plenum Press, New York, N.Y., 1973, Chapters 3 and 4, respectively, and T. W. Greene and P. G. M. Wuts, "Protective Groups in Organic Synthesis,” Second Edition, John Wiley and Sons, New York, N.Y., 1991, Chapters 2 and 3.
  • the following Table shows the chemical structure of some protecting groups, as well as nomenclature used to identify those chemical structures.
  • alkyl refers to a hydrocarbon structure wherein the carbons are arranged in a linear, branched, or cyclic manner, including combinations thereof.
  • Lower alkyl refers to alkyl groups of from 1 to 5 carbon atoms. Examples of lower alkyl groups include methyl, ethyl, propyl, isopropyl, butyl, s- and t-butyl and the like.
  • Preferred alkyl groups are those of C20 or below. More preferred alkyl groups are those of C13 or below.
  • Cycloalkyl is a subset of alkyl and includes cyclic hydrocarbon groups of from 3 to 13 carbon atoms.
  • cycloalkyl groups include cyclopropyl, cyclobutyl, cyclopentyl, norbornyl, adamantyl and the like.
  • alkyl residue having a specific number of carbons is named, all geometric isomers having that number of carbons are intended to be encompassed; thus, for example, "butyl” is meant to include n-butyl, sec-butyl, isobutyl and t-butyl; "propyl” includes n-propyl and isopropyl.
  • alkenyl refers to an alkyl group having at least one site of unsaturation, i.e., at least one double bond.
  • alkynyl refers to an alkyl group having at least one triple bond between adjacent carbon atoms.
  • alkoxy and “alkoxyl” both refer to moieties of the formula -O-alkyl. Examples include methoxy, ethoxy, propoxy, isopropoxy, cyclopropyloxy, cyclohexyloxy and the like. Lower-alkoxy refers to groups containing one to four carbons.
  • aryloxy refers to moieties of the formula -O-aryl.
  • One or more carbons in the acyl residue may be replaced by nitrogen, oxygen or sulfur as long as the point of attachment to the parent remains at the carbonyl.
  • Examples include acetyl, benzoyl, propionyl, isobutyryl, t- butoxycarbonyl, benzyloxycarbonyl and the like.
  • Lower-acyl refers to groups containing one to four carbons.
  • aryl refers to phenyl or naphthyl.
  • Substituted aryl refers to mono- and poly- substituted phenyl or naphthyl.
  • Exemplary subsituents for aryl include one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms.
  • heteroaryl refers to a 5- or 6-membered heteroaromatic ring containing 1-3 heteroatoms selected from O, N, or S; a bicyclic 9- or 10-membered heteroaromatic ring system containing 0-3 heteroatoms selected from O, N, or S; or a tricyclic 13- or 14-membered heteroaromatic ring system containing 0-3 heteroatoms selected from O, N, or S.
  • Exemplary aromatic heterocyclic rings include, e.g., imidazole, pyridine, indole, thiophene, benzopyranone, thiazole, furan, benzimidazole, quinoline, isoquinoline, quinoxaline, pyrimidine, pyrazine, tetrazole and pyrazole.
  • the term "leaving group” (LG) refer to a chemical moiety that may be displaced during a substitution or elimination reaction.
  • Exemplary leaving groups include halide (e.g., bromide and chloride) and as tosyl.
  • halogenating agent refers to a chemical that may be added to a reaction mixture to cause the addition of a halide to a carbon of an organic molecule.
  • Halogenating agents include, for example, inorganic acid halides, for example thionyl chloride, phosphorus trichloride, phosphorus tribromide, phosphoryl chloride trifluoromethanesulfonic acid, N- iodosuccinimide and phosphorus pentachloride. Other halogenating are known in the art.
  • the reaction is conveniently carried out in the presence of an excess of the halogenating agent in the presence of a solvent or diluent such as, for example, a halogenated solvent such as methylene chloride, chloroform or carbon tetrachloride.
  • a solvent or diluent such as, for example, a halogenated solvent such as methylene chloride, chloroform or carbon tetrachloride.
  • the reaction may conveniently carried out at a temperature in the range, for example, 10 to 150°C, preferably in the range 40 to 100°C.
  • the present invention provides compounds including the designation "-CO 2 -E" where E represents hydrogen or an organic group.
  • the compounds being disclosed are carboxylic acids or esters thereof.
  • E is hydrogen.
  • E is an organic group, where preferred organic groups are alkyl, alkenyl, alkynyl, aryl, or heteroaryl as defined above.
  • E has a molecular weight of less than 1 ,000, preferably less than 500 g/mol.
  • the present invention provides for the preparation of imine compounds, the conversion of an imine compound to a ⁇ - lactam compound, the preparation of oxime compounds, the conversion of an oxime compound to a ⁇ -lactam, the conversion of one ⁇ -lactam compound to another ⁇ -lactam compound, the ring-opening of a ⁇ -lactam compound to provide a 3-phenylisoserine compound, and the conversion of one 3- phenylisoserine compound to another 3-phenylisoserine compound.
  • reaction of benzaldehyde with anisidine yields a para-methoxyphenyl (PMP)- protected imine.
  • the present invention provides a process of forming a beta lactam of the formula
  • An and Ar 2 are each aryl groups, where each of An and Ar 2 are independently optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbon atoms, and aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon atoms.
  • each of An and Ar 2 are phenyl.
  • Reaction 2 an aspect of the present invention is illustrated by Reaction 2, wherein an imine may be prepared by reacting benzaldehyde with ammonia.
  • the present invention provides a process of preparing a beta-lactam, comprising the scheme
  • Ri is hydroxyl, protected hydroxyl, thiol, or protected thiol; LG is a leaving group;
  • R 2 is alkyl, alkenyl, alkynyl, or aryl where R 2 is optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms; and R 3 is hydrogen.
  • Ri is thioaryl or substituted thioaryl, e.g., thiophenyl or substituted thiophenyl. In one embodiment of the invention, Ri is thiophenyl.
  • R 2 is aryl or substituted aryl, e.g., phenyl or substituted phenyl. In one embodiment of the invention, R 2 is phenyl.
  • the scheme shows the formation of the cis product (i.e., Ri and R 2 are cis), however it is typically the case that both the cis and trans products are formed.
  • Reaction 3 shows a specific example of converting an imine to a ⁇ -lactam, where this specific conversion is another aspect of the present invention.
  • an imine is dissolved in an inert solvent such as dichloromethane and cooled to about 0°C under an inert atmosphere such as argon gas.
  • Thiophenyl acetyl chloride or any other respective acid chloride is added dropwise to the cooled stirred solution of the imine at about 0°C.
  • a tertiary amine e.g., triethylamine, also at about 0°C.
  • the reaction mixture is gradually warmed to room temperature and kept at this temperature for about 16 hours.
  • the reaction is quenched by pouring into ice-cold water and extracted three times with dichloromethane and dried over anhydrous magnesium sulfate.
  • the solvent is evaporated to give the crude product which is purified by column chromatography using dichloromethane initially followed by mixtures of hexane/ethyl acetate to get the pure cis and trans ⁇ -lactams shown in Reaction 3.
  • the cis and trans isomers may be separated from one another by, e.g.,. column chromatography. Either isomer, or the mixture of isomers, may be converted to a phenylisoserine compound as described later herein.
  • the present invention also provides compounds of the formula
  • R ⁇ is thiol (SH), tBOC, acetate, methoxy, thiophenyl, CI 2 CH-C(O)O- or 1 -ethoxyethyl, R 2 is phenyl and R 3 is hydrogen.
  • an imine without a protecting group attached to the imine nitrogen may be converted to a ⁇ -lactam as shown in Reaction 4, where this conversion is another aspect of the invention, and the chemical product is another aspect of the invention.
  • acetoxy acetyl chloride dropwise at about 0°C.
  • a tertiary amine such as triethylamine
  • the reaction mixture is gradually warmed to room temperature and kept at this temperature for overnight.
  • the reaction is quenched by pouring into ice- cold water and extracted three times with dichloromethane following by drying over anhydrous magnesium sulfate.
  • the solvent is evaporated to give the crude product which may be purified by column chromatography using dichloromethane initially followed by mixtures of hexane/ethyl acetate to give the ⁇ -lactam.
  • an oxime compound is converted to a protected form as illustrated in Reaction 5.
  • a syn-benzaldehyde oxime is added to a stirred solution of NaH in anhydrous THF at 0°C under an argon atmosphere.
  • the reaction mixture is stirred at this temperature for 20 minutes and then (BOC) 2 is added dropwise.
  • the reaction is stirred at 0°C for 1 hr and worked up as usual.
  • the crude product is purified by column chromatography using hexane/dichloromethane to afford the pure product.
  • the present invention provides a process for preparing a beta lactam, comprising the scheme
  • Ri is hydroxyl, protected hydroxyl, thiol, or protected thiol; LG is a leaving group;
  • R 2 is alkyl, alkenyl, alkynyl or aryl, where R 2 may be optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms; and PG is a protecting group. Noteworthy is that this process provides beta-lactam compounds having -O-PG substitution at the heterocyclic nitrogen ring.
  • an oxime compound is converted to a beta-lactam having oxygen substitution on the ring nitrogen, as shown in Reaction 6.
  • a protected oxime is dissolved in dichloromethane and cooled to 0°C under argon atmosphere.
  • Acetoxy acetyl chloride or any other acid chloride is added dropwise to the cooled stirred solution of the oxime at 0°C.
  • DMAP or any other base is added dropwise to this solution.
  • the reaction mixture is gradually warmed to room temperature (or may be heated to about 40°C) and keep at this temperature for 16 hours.
  • the reaction is quenched by pouring into ice-cold water and extracted three times with dichloromethane and dried over anhydrous magnesium sulfate.
  • the present invention provides compounds of the formula
  • Ri is hydroxyl, protected hydroxyl, thiol, or protected thiol
  • R 2 is alkyl, alkenyl, alkynyl or aryl, where R 2 may be optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms; and PG is a protecting group.
  • Ri is a protected hydroxyl group and the protecting group is selected from methoxymethyl, methoxyethyl, 1- ethoxyethyl, benzyloxymethyl, (beta-trimethylsilyl-ethoxy)methyl, tetrahydropyranyl, 2,2,2-trichloro-ethoxycarbonyl, benzyloxycarbonyl, tert- butoxycarbonyl, 9-fluorenylmethoxycarbonyl, 2,2,2-trichloroethoxymethyl, trimethylsilyl, triethylsilyl, tripropylsilyl, dimethylethylsilyl, dimethyl(t-butyl)silyl, diethylmethylsilyl, dimethylphenylsilyl, diphenylmethylsilyl, acetyl, chloroacetyl, dichloroacetyl, trichloroacetyl and trifluoroacetyl.
  • the protecting group is selected from
  • Ri is a protected thiol group, and the protecting group is selected from triphenylmethyl (trityl, Trt), acetamidomethyl (Acm), benzamidomethyl, 1 -ethoxyethyl and benzoyl. 5. Conversion of a beta-lactam compound to a different beta-lactam compound
  • a thiophenyl-substituted ⁇ -lactam having a protecting group on the ring nitrogen may be deprotected as shown in Reaction 7, where this deprotection reaction is another aspect of the present invention.
  • cis beta lactam is dissolved in a suitable solvent such as acetonitrile under an inert atmosphere such as argon gas, and cooled to about 0°C.
  • a suitable solvent such as acetonitrile under an inert atmosphere such as argon gas
  • CAN eerie ammonium nitrate
  • the reaction mixture is poured into water and extracted three times with ethyl acetate.
  • the combined organic phases are successively washed with (a) 5% sodium bicarbonate solution, (b) saturated sodium sulfate solution, and (c) saturated sodium chloride solution, followed by drying over anhydrous sodium sulfite.
  • the present invention provides a process whereby the nitrogen atom of a beta-lactam is bonded to a protecting group. This aspect of the invention comprises treating a beta lactam of the structure
  • beta lactam of the structure wherein An and Ar 2 are aryl groups independently selected at each occurrence, and R 5 is selected from benzoyl and tBOC.
  • the protecting agent may be, for example, benzoyl chloride or di-tert-butyl-dicarbonate.
  • this process is proceeded by forming a beta lactam of the formula
  • the base may be a nitrogen-containing base, e.g., ammonia.
  • the ring nitrogen of a ⁇ -lactam may be protected with an amine protecting group such as benzoyl (Bz, as shown in the following reaction) or t-BOC. This is illustrated in Reaction 8.
  • an amine protecting group such as benzoyl (Bz, as shown in the following reaction) or t-BOC. This is illustrated in Reaction 8.
  • a ⁇ -lactam is dissolved in an inert solvent such as dichloromethane and cooled to ca. 0°C under an inert atmosphere, e.g., argon gas.
  • Dimethylaminopyridine (DMAP) and triethylamine are added followed by dropwise addition of benzoyl chloride at 0°C with stirring.
  • the reaction mixture is stirred for about 1 hour and then was washed with saturated aqueous ammonium chloride and brine and dried over anhydrous sodium sulfate. After removal of the solvent under reduced pressure the crude product is purified by column chromatography using mixtures of dichloromethane/hexane to afford the pure benzoylated ⁇ -lactam.
  • a paramethoxyphenyl protecting group attached to the ring nitrogen of a ⁇ -lactam is replaced with a benzoyl group as shown in Reaction 9.
  • the paramethoxy group of the trans ⁇ -lactam is removed by using eerie ammonium nitrate (CAN) in aqueous acetonitrile solution, followed by treating the product mixture with benzoyl chloride to afford a mixture of cis and trans benzoylated ⁇ -lactams.
  • CAN eerie ammonium nitrate
  • the present invention provides for the halogenation of a beta-lactam, as illustrated by the scheme
  • An and Ar 2 are each aryl groups, where each of An and Ar 2 is independently optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbon atoms, and aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon atoms;
  • X is halide;
  • R 5 is selected from hydrogen, benzoyl and tBOC, and M is a halogenating agent.
  • each of An and Ar 2 is phenyl.
  • exemplary halogenating agents include, without limitation, inorganic acid halides, for example thionyl chloride, phosphorus trichloride, phosphorus tribromide, phosphoryl chloride trifluoromethanesulfonic acid, N-iodosuccinimide and phosphorus pentachloride.
  • the halogenating agent is SO 2 CI 2 .
  • a trans thiophenyl ⁇ -lactam can be modified by introducing a chloro group at the 3-position as shown in Reaction 10.
  • a trans thiophenyl beta lactam is dissolved in an inert solvent, e.g., anhydrous dichloromethane, under an inert atmosphere, e.g., argon gas, and cooled to about 0°C.
  • an inert atmosphere e.g., argon gas
  • Sulfuryl chloride is added dropwise to the stirred solution at ca. 0°C and left at this temperature for ca. 2 hrs.
  • the solvent is evaporated and the residue dissolved in dichloromethane and washed successively with water, 10% sodium bicarbonate, saturated brine and dried over anhydrous sodium sulfate. After removal of the solvent under reduced pressure the crude solid is purified by recrystallization using mixtures of diehloromethane/hexanes to give the chloro group at the 3-position of the trans thiophenyl beta lactam.
  • An and Ar 2 are each aryl groups, where each of An and Ar 2 are independently optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbon atoms, and aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon atoms;
  • X is halide; and R 5 is selected from hydrogen, benzoyl, tBOC, C ⁇ -C 6 alkyl or aryl where R5 is optionally substituted with one or more halogens, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyan
  • the present invention provides a process wherein a halide substituent on a beta-lactam ring is replaced with a protected hydroxyl group, as illustrated by the following scheme
  • An and Ar 2 are each aryl groups, where each of An and Ar 2 are independently optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbon atoms, and aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon atoms; M is metal and X is one or more halides attached to the metal; R 5 is selected from hydrogen, benzoyl and tBOC; and Re is CI-C ⁇ alkyl.
  • An and Ar 2 are each phenyl.
  • the present invention provides that a chloro- substituted beta-lactam may be converted into the corresponding beta-lactam where the chloride group is replaced with an acetate group. This conversion is illustrated in Reaction 11. Reaction 11
  • the chloro-substituted beta-lactam is dissolved in an inert solvent, e.g., anhydrous dichloromethane, at room temperature under an inert atmosphere, e.g., argon atmosphere.
  • an inert solvent e.g., anhydrous dichloromethane
  • silica gel zinc chloride
  • an alkyl anhydride e.g., acetic anhydride as shown in reaction XI lb.
  • the reaction mixture is left at this temperature for ca. 16 hrs and then worked up.
  • the silica gel is filtered and the filtrate evaporated, dissolved in dichloromethane and worked up as usual for this type of reaction.
  • the crude residue is purified by column chromatography using mixtures of hexanes/ethyl acetate to afford the pure product.
  • An and Ar 2 are each aryl groups, where each of An and Ar 2 are independently optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbon atoms, and aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon atoms;
  • R 5 is selected from hydrogen, benzoyl and tBOC; and
  • R 9 is a hydroxyl protecting group.
  • Rg is selected from methoxymethyl, methoxyethyl, 1 -ethoxyethyl, benzyloxymethyl, (beta-trimethylsilyl-ethoxy)methyl, tetrahydropyranyl, 2,2,2- trichloro-ethoxycarbonyl, benzyloxycarbonyl, ferf-butoxycarbonyl, 9- fluorenylmethoxycarbonyl, 2,2,2-trichloroethoxymethyl, trimethylsilyl, triethylsilyl, tripropylsilyl, dimethylethylsilyl, dimethyl(t-butyl)silyl, diethylmethylsilyl, dimethylphenylsilyl, diphenylmethylsilyl, acetyl, chloroacetyl, dichloroacetyl, trichloroacetyl and trifluoroacetyl.
  • the protecting group of an N- protected beta lactam is replaced with a different protecting group, as shown in Reaction 12.
  • a paramethoxyphenyl (PMP) group is cleaved by using the procedure as in Reaction 7.
  • the product obtained from this cleavage is dissolved in an inert solvent, e.g., anhydrous dichloromethane, at ca. room temperature under argon atmosphere.
  • an inert solvent e.g., anhydrous dichloromethane
  • DMAP dropwise benzoyl chloride
  • the reaction mixture is worked up as usual and purified by column chromatography using mixtures of hexanes/ethyl acetate to afford the pure benzoylated beta lactam
  • the thiophenyl group of a thiophenyl-substituted beta lactam is removed using a desulfurization reagent, and a hydrogen put in its place.
  • a desulfurization reagent is Raney Ni.
  • a thiophenyl-substituted beta lactam is dissolved in ethanol at room temperature and Raney nickel is added in one portion to the stirred solution and the reaction mixture is stirred at this temperature for about 2 hrs.
  • the reaction mixture is filtered and the filtrate is evaporated.
  • the residue is dissolved in an inert solvent such as dichloromethane and worked up as usual.
  • the crude product is purified by column chromatography using mixtures of hexanes/ethyl acetate to afford the pure product. Often, the product will be obtained as a mixture of N-protected and N-deprotected beta lactams.
  • a beta lactam with oxygen substitution on the ring nitrogen is converted to the corresponding beta-lactam with hydrogen substitution on the ring nitrogen.
  • a beta lactam with oxygen substitution on the ring nitrogen is dissolved in methanol at room temperature and treated with Pd(OH) 2 -C (or any other reducing agent) and the resulting suspension is stirred under hydrogen atmosphere for overnight.
  • the reaction mixture is filtered through a pad of celite and the volatile component(s) of the filtrate are evaporated.
  • the residue was dissolved in dichloromethane and worked up as usual.
  • the crude product is purified by column chromatography using mixtures of hexanes/ethyl acetate to afford the pure beta lactam.
  • the present invention provides a process comprising the process disclosed in Reaction 15, wherein a thioaryl group is converted to a protected hydroxyl group
  • An and Ar 2 are independently selected from alkyl, alkenyl, alkynyl, aryl or substituted aryl radical; and R 10 is hydrogen, C ⁇ -C 6 alkyl, aryl or substituted aryl radical; wherein a substituted aryl radical is substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms.
  • a beta lactam with a phenylthio substitution on the ring is dissolved in an organic solvent at room temperature and treated with copper acetate.
  • the reaction mixture is filtered through a pad of celite and the volatile component(s) of the filtrate are evaporated.
  • the crude product is purified by column chromatography using mixtures of hexanes/ethyl acetate to afford the pure beta lactam.
  • the present invention provides a process comprising the process disclosed in Reaction 16 wherein a thioaryl group is converted to a hydroxyl group
  • Hg represents a mercuric reagent, e.g., mercuric oxide or mercuric trifluoroacetate
  • An and Ar 2 are independently selected from alkyl, alkenyl, alkynyl, aryl or substituted aryl radical
  • Rio is hydrogen, C ⁇ -C 6 alkyl, aryl or substituted aryl radical
  • a substituted aryl radical is substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms.
  • the mercuric reagent e.
  • the present invention provides a process of opening a beta-lactam ring.
  • the process may be illustrated by the following scheme
  • Ri is hydroxyl, protected hydroxyl, thiol, or protected thiol; LG is a leaving group; PG is an amino protecting group; R 2 is alkyl, alkenyl, alkynyl, or aryl where R 2 is optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms; R 3 is hydrogen, C ⁇ -C 6 alkyl or aryl where R 3 is optionally substituted with one or more halogens, hydroxyl, alkoxy, aryloxy, heteroaryloxy,
  • the ring- opened product is purified by column chromatography followed by recrystallization, where the recystallization is preferably performed with an organic solvent.
  • the process may be performed in a mixture of organic solvent and aqueous acid.
  • Ri is thiophenyl
  • R 2 is phenyl
  • R 3 is hydrogen.
  • the present invention provides for the conversion of a ⁇ -lactam with thiophenyl substitution to the corresponding phenylisoserine compound as shown in Reaction 17.
  • Reaction 17 the conversion of a ⁇ -lactam with thiophenyl substitution to the corresponding phenylisoserine compound as shown in Reaction 17.
  • a ⁇ -lactam is dissolved in a minimum volume of DMSO or mixtures of DMSO/DCM and hydrochloric acid is added.
  • the stirred reaction mixture is heated to about 85°C for ca. 16 hrs.
  • the reaction mixture is cooled to room temperature and dried under vacuum to give a powder, which is the salt of an intermediate compound of the structure
  • This powder is dissolved in pyridine under an inert atmosphere (e.g., argon) and benzoyl chloride is added dropwise at room temperature.
  • the reaction mixture is stirred at this temperature for about 2 hrs.
  • the reaction mixture is acidified with 0.1N HCI and the crude product is extracted with dichloromethane.
  • the combined organic extracts are dried over anhydrous magnesium sulfate and concentrated in vacuo to dryness.
  • the crude product is purified by column chromatography using hexane/ethyl acetate and dichloromethane/ methanol to afford the pure cis phenylisoserine side chain.
  • ring-opening of a ⁇ -lactam provides a phenylisoserine compound as illustrated in Reaction 18.
  • trans ⁇ -lactam treatment of a trans ⁇ -lactam with protic acid followed by reaction with benzoyl chloride in base (e.g., pyridine) affords a trans phenylisoserine side chain.
  • base e.g., pyridine
  • the present invention provides a process wherein a beta-lactam having both thiophenyl and protected hydroxyl substitution is converted to a ring-opened form, as illustrated by the following scheme
  • An and Ar 2 are aryl groups independently selected at each occurrence, R 5 is selected from hydrogen, benzoyl and tBOC, R 6 is a hydroxy protecting group, and R 7 is hydrogen or Ci-Cealkyl, where R as C ⁇ -C 6 alkyl is introduced in an optional esterification reaction.
  • H+ represents a proton source, e.g., mineral acid or organic acid.
  • An and Ar 2 are each phenyl.
  • the present invention provides a process of opening a beta lactam according to the scheme
  • PG is a hydroxyl protecting group
  • An and Ar 2 are each aryl groups, where each of An and Ar 2 are independently optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbon atoms, and aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon atoms; and Ri is hydrogen, alkyl, or -O-PG wherein PG is a protecting group.
  • a beta-lactam is ring- opened to afford the corresponding phenylisoserine compound as shown in Reaction 19.
  • the paramethoxyphenyl (PMP) group of the beta-lactam shown in Reaction 19 is cleaved by using the procedure as in Reaction 7.
  • the product obtained from this cleavage is dissolved in a minimum volume of dichloromethane at room temperature and a solution of hydrochloric acid is added.
  • the stirred solution is heated to about 60°C for about 3 hrs.
  • the reaction mixture is cooled to room temperature and concentrated in vacuo to dryness, giving the acid as a powder.
  • the present invention provides a process whereby a beta lactam having oxygen substitution on the ring nitrogen is converted into a phenylisoserine compound, as illustrated in Reaction 20.
  • Ri is hydroxyl, protected hydroxyl, thiol, or protected thiol
  • PG is an amino protecting group
  • R 2 is alkyl, alkenyl, alkynyl, or aryl where R 2 is optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms;
  • R 3 is hydrogen, C ⁇ -C 6 alkyl or aryl where R 3 is optionally substituted with one or more halogens, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alky
  • the isoserine compound is characterized by having Ri be hydroxyl or protected hydroxyl; R 2 be aryl; and R 3 be hydrogen; including salts and esters thereof.
  • the isoserine compound is characterized by having Ri be thiol or protected thiol; R be aryl; R 3 be hydrogen; and includes salts and esters thereof.
  • R 5 is selected from hydrogen, benzoyl and tBOC
  • R is a hydroxyl protecting group
  • R is hydrogen or CrC ⁇ alkyl.
  • Re is selected from methoxymethyl, methoxyethyl, 1 -ethoxyethyl, benzyloxymethyl, (beta- trimethylsilyl-ethoxy)methyl, tetrahydropyranyl, 2,2,2-trichloro-ethoxycarbonyl, benzyloxycarbonyl, fetf-butoxycarbonyl, 9-fluorenylmethoxycarbonyl, 2,2,2- trichloroethoxymethyl, trimethylsilyl, triethylsilyl, tripropylsilyl, dimethylethylsilyl, dimethyl(t-butyl)silyl, diethylmethylsilyl, dimethylphenylsilyl, diphenylmethyls
  • Ar 2 is an aryl group
  • R 5 is selected from hydrogen, benzoyl and tBOC
  • R 6 is a thiol protecting group
  • R 7 is H or C ⁇ -C 6 alkyl.
  • the thiol protecting group is triphenylmethyl (trityl, Trt), acetamidomethyl (Acm), benzamidomethyl, 1 -ethoxyethyl or benzoyl.
  • the present invention provides a process whereby a thioaryl group in a phenylisoserine compound is replaced with a hydroxyl group, as shown in the following Reaction 21.
  • PG is an amine protecting group
  • An and Ar 2 are aryl groups
  • E is hydrogen or an organic group
  • Hg represents a mercury-containing oxidizing agent.
  • PG is benzoyl or tBOC
  • E is hydrogen
  • An is phenyl
  • Ar 2 is phenyl.
  • Two exemplary mercuric oxidizing agents are HgO and Hg(CF 3 CO 2 ) 2 .
  • the present invention provides that a thiophenyl group located at the 2-position of a 3-phenylisoserine may be replaced with a hydroxyl group of the opposite configuration, as shown in Reaction 22.
  • a trans 2-thiophenyl 3-phenylisoserine compound is dissolved in an inert solvent, e.g., freshly distilled THF, under an inert atmosphere, e.g., argon gas, and a mercury-containing oxidizing agent, e.g., mercuric oxide (HgO) or Hg(CF 3 CO 2 ) 2 as shown in Reaction 22, is added in one portion at room temperature and the reaction mixture stirred at this temperature for about 72 hrs.
  • an inert solvent e.g., freshly distilled THF
  • an inert atmosphere e.g., argon gas
  • a mercury-containing oxidizing agent e.g., mercuric oxide (HgO) or Hg(CF 3 CO 2 ) 2 as shown in Reaction 22
  • reaction is worked up according to procedures known in the art for reactions with mercuric oxidizing agent, and the product is purified by column chromatography using mixtures of acetone/methanol to afford the pure cis phenylisoserine side chain.
  • the present invention provides a process whereby a hydroxyl group in a phenylisoserine compound is converted to a protected hydroxyl group, as shown in Reaction 23.
  • PGi is an amine protecting group
  • An and Ar 2 are aryl groups
  • E is hydrogen or an organic group
  • PG 2 is a hydroxyl protecting group
  • PG 2 -X represents a reagent that introduces a protecting group onto a hydroxyl group.
  • PGi is benzoyl or tBOC
  • E is hydrogen
  • An is phenyl
  • Ar 2 is phenyl and/or PG 2 is acetyl.
  • An exemplary reagent to add a protecting group onto a hydroxyl group is acetyl chloride.
  • Other reagents are well known in the art, including those set forth in T. W. Greene and P. G. M.
  • the present invention provides for the acylation of the 2-hydroxy group of a 3-phenyl-2-hydroxy isoserine compound, as shown in Reaction 24.
  • a cis phenylisoserine compound is dissolved in a basic solvent, e.g., pyridine, under an inert atmosphere, e.g., argon gas, at about room temperature and acetyl chloride is added dropwise to the stirred solution.
  • a basic solvent e.g., pyridine
  • an inert atmosphere e.g., argon gas
  • the solution is stirred for about 30 minutes and worked up according to methods known in the art for acylation reaction.
  • the crude product is purified by column chromatography using mixtures of dichloromethane/methanol to afford the pure acetylated cis phenylisoserine side chain acid.
  • the present invention provides a process whereby a thioaryl group is removed from an arylisoserine compound, as illustrated by the scheme
  • An and Ar 2 are aryl groups independently selected at each occurrence, R 5 is selected from hydrogen, benzoyl and tBOC, Re is C ⁇ -C 6 alkyl, R 7 is H or C ⁇ -C 6 alkyl, and E represents a desulfuration reagent. Raney nickel is a suitable desulfurization reagent.
  • each of An and Ar 2 is phenyl.
  • the present invention provides a process whereby a thioaryl group is removed from an arylisoserine compound as illustrated by the scheme of Reaction 25. Reaction 25
  • An and Ar 2 are aryl groups, E is hydrogen or an organic group, and OPG represents a protected hydroxyl group.
  • An is phenyl, and/or Ar 2 is phenyl, and/or E is hydrogen and/or PG is acetyl or ethoxyethyl (EE).
  • R 5 is selected from hydrogen, benzoyl and tBOC
  • R 6 is a hydroxyl protecting group
  • R is H or C ⁇ -C 6 alkyl.
  • R 6 is selected from methoxymethyl, methoxyethyl, 1 -ethoxyethyl, benzyloxymethyl, (beta-trimethylsilyl-ethoxy)methyl, tetrahydropyranyl, 2,2,2-trichloro- ethoxycarbonyl, benzyloxycarbonyl, te/f-butoxycarbonyl, 9- fluorenylmethoxycarbonyl, 2,2,2-trichloroethoxymethyl, trimethylsilyl, triethylsilyl, tripropylsilyl, dimethylethylsilyl, dimethyl(t-butyl)silyl, diethylmethylsilyl, dimethylphenylsilyl, diphenylmethylsilyl,
  • the present invention provides a process whereby a protecting group is added to the amino group of an arylisoserine compound, as illustrated in the scheme of Reaction 26.
  • Reaction 26
  • An and Ar 2 are aryl groups, E is hydrogen or an organic group, PGi represents a hydroxyl protecting group and PG2 represents an amine protecting group.
  • An is phenyl, and/or Ar 2 is phenyl, and/or E is hydrogen and/or PGi is acetyl.
  • PG 2 is a benzoyl group.
  • taxotere is the target taxane
  • PG 2 is a tBOC group.
  • a protecting group is added to the amine group of a 3-arylisoserine compound, and a thioaryl group is removed from the alpha carbon, as illustrated in Reaction 27, where phenyl is shown as a representative aryl group, acetate is shown as a representative hydroxyl protecting group, and benzoyl is shown as a representative amine protecting group.
  • a phenylisoserine compound is dissolved in ethanol at room temperature and Raney nickel is added in one portion to the stirred solution and the reaction mixture is stirred at this temperature for 3 hrs.
  • the reaction mixture is filtered and the filtrate is evaporated.
  • the residue is dissolved in dichloromethane and worked up as usual.
  • This resulting solid is dissolved in pyridine under argon atmosphere and benzoyl chloride added dropwise at room temperature.
  • the reaction mixture is stirred at this temperature for about 4 hrs.
  • the reaction mixture is acidified with 0.1N HCI and the crude product is extracted with dichloromethane. The combined organic extracts are dried over anhydrous magnesium sulfate and concentrated in vacuo to dryness.
  • the crude product is purified by column chromatography using dichloromethane/methanol to afford the pure cis 2'-acetylated phenylisoserine side chain.
  • a reagent that adds a tBOC group to an amine group may be used in lieu of benzoyl chloride.
  • the protecting group on the nitrogen atom of a 3-phenylisoserine compound is replaced with a different protecting group as illustrated in Reaction 28.
  • a O-t-BOC protected phenylisoserine compound is treated under reducing conditions as shown in reaction 28, and then benzoylated using benzoyl chloride in pyridine according to reaction 27 to give the 2'-protected phenylisoserine taxol side chain.
  • This compound is a useful intermediate in the production of taxanes.
  • This compound may be prepared according to Reaction 29, which is another aspect of the present invention.
  • the base may be an amine base, e.g., dimethylaminopyridine (DMAP).
  • DMAP dimethylaminopyridine
  • the reaction is typically conducted in an inert solvent, e.g., dichloromethane (DCM).
  • DCM dichloromethane
  • Baccatin III may be dissolved in anhydrous dichloromethane under an argon atmosphere at room temperature. To this solution is added DMAP followed by dichloroacetyl chloride. The mixture is left at room temperature for overnight. The mixture is then quenched with cold water and extracted thrice with dichloromethane. The organic layer is washed with water and than with brine to remove unwanted salts. The organic layer may then be dried and evaporated under vacuum, and the residue recrystallized or column chromatographed with dichloromethane/ethyl acetate mixtures to afford C7 protected baccatin III.
  • DCM dichloromethane
  • C7 protected baccatin III or C7 and C10 protected baccatin III can also be prepared from 10 DAB or 9DHB (9-dihydro- 13-acetylbaccatin III) in a similar manner.
  • This compound is a useful intermediate in the production of taxanes.
  • This compound may be prepared according to Reaction 30, which is another aspect of the present invention.
  • the base may be an amine base, e.g., dimethylaminopyridine (DMAP) or pyridine.
  • DMAP dimethylaminopyridine
  • the reaction is typically conducted in an inert solvent, e.g., dichloromethane (DCM).
  • DCM dichloromethane
  • Baccatin III may be dissolved in anhydrous dichloromethane under an argon atmosphere at room temperature. To this solution is added pyridine followed by triethylsilyl chloride. The mixture is left at room temperature for overnight. The mixture is then quenched with cold water and extracted thrice with dichloromethane. The organic layer is washed with water and than with brine to remove unwanted salts.
  • the present invention provides for the coupling of a sidechain as described in the previous section, which may be either a beta lactam or a phenylisoserine, with a baccatin-type compound.
  • a sidechain as described in the previous section, which may be either a beta lactam or a phenylisoserine
  • baccatin-type compound is described by the formula
  • Re and R are selected from hydrogen and hydroxy protecting groups.
  • the sidechain couples to the baccatin-type compound at the hydroxyl group located at C13 of the baccatin-type compound.
  • Re is acetyl and R is tnethylsily (TES);
  • R 6 is acetyl and R is -COCHCI 2 ;
  • R 6 is dichloroacetyl and R is tnethylsily (TES); or
  • Re is dichloroacetyl and R 7 is -COCHCI 2 .
  • the coupling is performed in the presence of a dialkylcarbodiimide, e.g., dicyclohexylcarbodiimide.
  • the intermediate of formula (III") or (IV") is further modified to yield paclitaxel or analogs thereof.
  • the R group at the C7 position and the R group at the C2' site may be converted to hydroxyl groups to yield paclitaxel.
  • these coupling reactions are accomplished under the influence of a dialkylcarbodiimide, e.g., DCC.
  • reaction of a beta lactam may be accomplished by reacting with a C7 protected baccatin III (Schemes I and II below) to yield an intermediate of the following formula (Ilia”) or (1Mb") or (IVa") or (IVb M ): wherein R is acetyl, R 7 is a hydroxy protecting group, and Re is benzoyl (compound Ilia”) or t-BOC (compound lllb"); and
  • R is acetyl
  • R 7 is a hydroxy protecting group
  • R 8 is benzoyl (compound IVa") or t-BOC (compound IVb").
  • R 7 OTES or OCOCHCl 2
  • R 3 is H, SPh, OH, OAc or ethoxyethyl
  • R 4 is H or SPh
  • R 7 is O-TES or OCOCHCI 2 .
  • the beta lactam of formula lib obtained as described previously
  • the C7 protected baccatin III is dissolved in anhydrous freshly distilled THF under argon atmosphere at room temperature. This stirred solution is cooled to 0°C and added to a suspension of NaH in THF at 0°C. The solution is warmed slowly to room temperature and maintained at this temperature for 3 hrs. The reaction mixture was cooled to 0°C and quenched with brine.
  • the reaction mixture was extracted with dichloromethane and the combined extracts were washed several times with brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to give the crude product.
  • the crude product was purified by column chromatography using mixtures of hexanes/ethyl acetate to afford the pure coupled intermediate taxane of formula III" or IV" that could be converted to taxol or its analogs.
  • the coupling is performed in the presence of a metal base salts, e.g., a metal hexamethyldisilazide (e.g., LiHMDS, NaHMDS, KHMDS), or a Lewis acid, e.g., boron trifluoride etherate.
  • a metal base salts e.g., a metal hexamethyldisilazide (e.g., LiHMDS, NaHMDS, KHMDS)
  • a Lewis acid e.g., boron trifluoride etherate.
  • Scheme 2 is suited for the preparation of paclitaxel since the nitrogen atom of the beta-lactam is protected with a benzoyl (Bz) group.
  • the process of Scheme 2 is performed with the nitrogen atom of the beta-lactam being protected by a t-BOC protecting group, where this embodiment is well- suited for the preparation of taxotere.
  • R represents hydrogen or an organic group, e.g., R may be hydroxyl, protected hydroxyl, thiol, or protected thiol; alternatively R may be alkyl, alkenyl, alkynyl or aryl, where R may be optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms
  • R is selected as appropriate for the preparation of paclitaxel or taxotere.
  • DCC is shown as the coupling reagent in Schemes 3 and 4 for illustrative purpoes, however, other dialkylcarbodiimides may be used in lieu of, or in combination with, dicyclohexylcarbodiimide (DCC).
  • R 3 H or SPh or OH or OAc
  • R 4 H or SPh
  • R 7 OTES or OCOCHCl 2
  • R, H or SPh or OH or OAc
  • R 2 H or SPh
  • R 7 OTES or OCOCHCl 2

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Abstract

Disclosed are compounds of formula having utility as intermediates in the preparation of paclitaxel, taxotere and analogs thereof, and intermediates thereof.

Description

NOVEL TAXANES AND METHODS RELATED TO USE AND PREPARATION THEREOF
BACKGROUND OF THE INVENTION
Field of the Invention
The present invention relates generally to taxanes, compounds useful in the preparation of taxanes, and synthetic methods useful in the preparation of taxanes.
Description of the Related Art
The taxane family of terpenes has received much attention in the scientific and medical community because members of this family have demonstrated broad spectrum anti-leukemic and tumor-inhibitory activity. A well-known member of this family is paclitaxel, which has the following structure,
Figure imgf000003_0001
wherein Ac is acetyl, Bz is benzoyl, Ph is phenyl, the 2' position has the R configuration and the 3' position has the S configuration. Paclitaxel was first isolated from the bark of the pacific yew tree (Taxus brevifolia) in 1971 , and has proved to be a potent natural anticancer agent. For example, paclitaxel has been found to have activity against different forms of leukemia and against solid tumors in the breast, ovary, brain, and lung in humans.
This activity has stimulated an intense research effort over recent years, including the search for other taxanes having similar or improved properties, and the development of synthetic pathways for making taxanes such as paclitaxel. One result from this research effort was the discovery of an analog of paclitaxel called taxotere. Taxotere has been found to have very good anti-tumor activity and better bio-availability than paclitaxel. Taxotere is similar in structure to paclitaxel, having t-butoxycarbonyl instead of benzoyl on the amino group at the 3' position, and a hydroxyl group instead of the acetoxy group at the C-10 position (see EP 253738 for a discussion of taxotere).
Taxanes are structurally complicated molecules, and the development of commercially viable synthetic methods to make taxanes has been a challenge. Semi-synthetic pathways have been developed, where these methods begin with the isolation of a naturally occurring material and then the conversion of that material to the taxane of interest. One such pathway for the semi-synthesis of paclitaxel begins with 10-deacetylbaccatin III, a taxane isolated from the needles of the English yew tree (Taxus baccata). A semi-synthetic route for the production of taxotere has been reported that involves coupling of N-tert-butoxycarbonyl-(2R, 3S)-3-phenylisoserine with 10- deacetylbaccatin III in conjunction with proper protecting groups (Tetrahedron Letters 33:5185, 1992). The synthesis of taxotere has also been reported using enantiomerically pure beta-lactams as intermediates (J. Org. Chem. 56:1681, 1991 ; Tetrahedron 48:6985, 1992).
While significant advances have been made in this field, there remain a need for improved synthetic techniques for the production of paclitaxel and analogs thereof such as taxotere. For example, existing semi-synthetic pathways for production of paclitaxel generally involve coupling of a suitable side chain precursor to the free hydroxyl group at position 13 of 10- deacetylbaccatin III. Fully synthetic pathways also employ addition of such side-chains in a similar way. Thus, there is a need for improved routes for the generation of such precursors of the C-13 side chain, particularly since this side-chain has been found to be an important structural feature. The present invention fulfils these needs and provides other related advantages.
BRIEF SUMMARY OF THE INVENTION
In one aspect, the present invention provides a process of preparing a beta-lactam, where the process comprises the scheme
Figure imgf000004_0001
wherein Ri is hydroxyl, protected hydroxyl, thiol, or protected thiol; LG is a leaving group; R2 is alkyl, alkenyl, alkynyl, or aryl where R2 is optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms; and R3 is hydrogen. Optionally, (R2)(H)C=N-R3 is prepared by reaction between an aldehyde of the formula R2-CHO, and an amine of the formula R3-NH2. Also optionally, Ri is phenyl and R2 is phenyl.
In another aspect, the present invention provides a compound of the formula
Figure imgf000005_0001
wherein R is thiol (SH), tBOC, acetate, methoxy, thiophenyl, CI2CH-C(O)O- or 1-ethoxyethyl, R2 is phenyl and R3 is hydrogen, and salts thereof.
In another aspect, the present invention provides a process of opening a beta-lactam ring, where the process comprises the scheme
Figure imgf000005_0002
wherein Ri is hydroxyl, protected hydroxyl, thiol, or protected thiol; LG is a leaving group; PG is an amine protecting group; R2 is alkyl, alkenyl, alkynyl, or aryl where R2 is optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms; R3 is hydrogen, Ci-Cβ alkyl or aryl where R3 is optionally substituted with one or more halogens, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms; and H+ is a proton source.
In another aspect, the present invention provides an isoserine compound of the formula
PG^ R3
Ή O
R.
wherein Ri is hydroxyl, protected hydroxyl, thiol, or protected thiol; PG is an amino protecting group; R2 is alkyl, alkenyl, alkynyl, or aryl where R2 is optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms; R3 is hydrogen, Ci-Cδ alkyl or aryl where R3 is optionally substituted with one or more halogens, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms; and salts and esters thereof. . In another aspect, the present invention provides a process of forming a beta lactam of the formula
Figure imgf000007_0001
wherein Ari and Ar2 are each aryl groups, where each of Ari and Ar2 are independently optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbon atoms, and aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon atoms; and where the process comprises reacting together compounds of the formula ArιS-CH2-C(=O)CI, NH3, and Ar2-CHO under conditions that form the beta lactam.
In another aspect, the present invention provides a process comprising the following scheme
Figure imgf000007_0002
wherein An and Ar2 are each aryl groups, where each of Aη and Ar2 is independently optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbon atoms, and aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon atoms; X is halide; R5 is selected from hydrogen, benzoyl and tBOC, and M is a halogenating agent. In another aspect, the present invention provides a compound of the formula
Figure imgf000008_0001
wherein Ari and Ar2 are each aryl groups, where each of An and Ar2 are independently optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbon atoms, and aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon atoms; X is halide; and R5 is selected from hydrogen, benzoyl tBOC, Cι-C6 alkyl or aryl where R5 is optionally substituted with one or more halogens, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms, and salts thereof.
In another aspect, the present invention provides a process comprising the scheme
Figure imgf000008_0002
wherein An and Ar2 are each aryl groups, where each of Aη and Ar2 are independently optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbon atoms, and aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon atoms; M is metal and X is one or more halides attached to the metal; R5 is selected from hydrogen, benzoyl and tBOC; and Re is Ci-Cβ alkyl.
In another aspect, the present invention provides a compound of the formula
Figure imgf000009_0001
wherein Ari and Ar2 are each aryl groups, where each of Ari and Ar2 are independently optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbon atoms, and aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon atoms; R5 is selected from hydrogen, benzoyl and tBOC; and Rg is a hydroxyl protecting group. Optionally, Rg is selected from methoxymethyl, methoxyethyl, 1-ethoxyethyl, benzyloxymethyl, (beta-trimethylsilyl-ethoxy)methyl, tetrahydropyranyl, 2,2,2-trichloro- ethoxycarbonyl, benzyloxycarbonyl, tetf-butoxycarbonyl, 9- fluorenylmethoxycarbonyl, 2,2,2-trichloroethoxymethyl, trimethylsilyl, triethylsilyl, tripropylsilyl, dimethylethylsilyl, dimethyl(t-butyl)silyl, d iethy Imethy Isi ly I , dimethylphenylsilyl, diphenylmethylsilyl, acetyl, chloroacetyl, dichloroacetyl, trichloroacetyl and trifluoroacetyl. In another aspect, the present invention provides a process comprising the scheme
Figure imgf000009_0002
wherein An and Ar2 are aryl groups independently selected at each occurrence, R5 is selected from hydrogen, benzoyl and tBOC, Re is a hydroxy protecting group, R is hydrogen or Ci-Cβalkyl, and H+ represents a proton source, e.g., an organic acid or mineral acid.
In another aspect, the present invention provides a process of opening a beta lactam according to the scheme
Figure imgf000010_0001
wherein PG is a hydroxyl protecting group; A and Ar2 are each aryl groups, where each of An and Ar2 are independently optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbon atoms, and aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon atoms; Ri is hydrogen, alkyl, or -O-PG wherein PG is a protecting group, and H+ represents a proton source, e.g., organic or mineral acid.
In another aspect, the present invention provides a compound of the formula
Figure imgf000010_0002
wherein An and Ar2 are each aryl groups, where each of An and Ar2 is independently optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbon atoms, and aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon atoms; Re is selected from hydrogen, benzoyl and tBOC; R6 is a hydroxyl protecting group, and R is hydrogen or C C6alkyl. Optionally, R6 is selected from methoxymethyl, methoxyethyl, 1- ethoxyethyl, benzyloxymethyl, (beta-trimethylsilyl-ethoxy)methyl, tetrahydropyranyl, 2,2,2-trichloro-ethoxycarbonyl, benzyloxycarbonyl, tert- butoxycarbonyl, 9-fluorenylmethoxycarbonyl, 2,2,2-trichloroethoxymethyl, trimethylsilyl, triethylsilyl, tripropylsilyl, dimethylethylsilyl, dimethyl(t-butyl)silyl, diethylmethylsilyl, dimethylphenylsilyl, diphenylmethylsilyl, acetyl, chloroacetyl, dichloroacetyl, trichloroacetyl and trifluoroacetyl.
In another aspect, the present invention provides a process comprising the scheme
Figure imgf000011_0001
wherein An and Ar2 are each aryl groups, where each of An and Ar2 is independently optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbon atoms, and aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon atoms; R5 is selected from hydrogen, benzoyl and tBOC, R6 is Cι-C6 alkyl, R7 is H or Cι-C6 alkyl, and E represents a desulfuration reagent.
In another aspect, the present invention provides a compound of the formula
NHR5 o
OR6
wherein Ar2 is an aryl group optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbon atoms, and aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon atoms; R5 is selected from hydrogen, benzoyl and tBOC; R6 is a hydroxyl protecting group, and R7 is H or Cι-C6 alkyl. Optional hydroxyl protecting groups for Re include, without limitation, methoxymethyl, methoxyethyl, 1-ethoxyethyl, benzyloxymethyl, (beta- trimethylsilyl-ethoxy)methyl, tetrahydropyranyl, 2,2,2-trichloro-ethoxycarbonyl, benzyloxycarbonyl, te/f-butoxycarbonyl, 9-fluorenylmethoxycarbonyl, 2,2,2- trichloroethoxymethyl, trimethylsilyl, triethylsilyl, tripropylsilyl, dimethylethylsilyl, dimethyl(t-butyl)silyl, diethylmethylsilyl, dimethylphenylsilyl, diphenylmethylsilyl, acetyl, chloroacetyl, dichloroacetyl, trichloroacetyl and trifluoroacetyl.
In another aspect, the present invention provides a compound of the formula
NHR5 O
SR6
wherein Ar2 is an aryl group optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbon atoms, and aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon atoms; R5 is selected from hydrogen, benzoyl and tBOC, R6 is a thiol protecting group, and R7 is H or Cι- C6 alkyl.
In another aspect, the present invention provides a process of substituting the nitrogen of a beta lactam, comprising treating a beta lactam of the structure
Figure imgf000012_0001
with a base and a protecting agent, to provide a beta lactam of the structure
Figure imgf000012_0002
wherein An and Ar2 are each aryl groups, where each of An and Ar2 is independently optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbon atoms, and aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon atoms; and R5 is selected from benzoyl and tBOC. Optionally, the protecting agent is benzoyl chloride or di-tert-butyl- dicarbonate. Optionally, this process is preceeded by forming a beta lactam of the formula
Figure imgf000013_0001
by a process comprising reacting together compounds of the formula AnS-CH2- C(=O)CI, base, and Ar2-CHO under conditions that form the beta lactam. Optionally, the base is ammonia.
In another aspect, the present invention provides a process for preparing a beta lactam, comprising the scheme
Figure imgf000013_0002
wherein Ri is hydroxyl, protected hydroxyl, thiol, or protected thiol; LG is a leaving group; R2 is alkyl, alkenyl, alkynyl or aryl, where R2 may be optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms; and PG is a protecting group. In another aspect, the present invention provides a compound of the formula
Figure imgf000014_0001
wherein Ri is hydroxyl, protected hydroxyl, thiol, or protected thiol; R2 is alkyl, alkenyl, alkynyl or aryl, where R2 may be optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms; and PG is a protecting group.
In another aspect, the present invention provides a process comprising the scheme
Figure imgf000014_0002
wherein Ri is hydroxyl, protected hydroxyl, thiol, or protected thiol; R2 is alkyl, alkenyl, alkynyl or aryl, where R2 may be optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms; and PG is a protecting group, where H+ represents a proton source such as organic or mineral acid.
In another aspect, the present invention provides a compound of the formula
Figure imgf000015_0001
wherein Ri is hydroxyl, protected hydroxyl, thiol, protected thiol, alkyl, alkenyl, alkynyl, or aryl where Ri is optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms; R2 is alkyl, alkenyl, alkynyl or aryl, where R2 may be optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms; PG is a protecting group; and salts and esters thereof. Optionally, Ri is selected from methoxymethyl, methoxyethyl, 1-ethoxyethyl, benzyloxymethyl, (beta-trimethylsilyl- ethoxy)methyl, tetrahydropyranyl, 2,2,2-trichloro-ethoxycarbonyl, benzyloxycarbonyl, te/f-butoxycarbonyl, 9-fluorenylmethoxycarbonyl, 2,2,2- trichloroethoxymethyl, trimethylsilyl, triethylsilyl, tripropylsilyl, dimethylethylsilyl, dimethyl(t-butyl)silyl, diethylmethylsilyl, dimethylphenylsilyl, diphenylmethylsilyl, acetyl, chloroacetyl, dichloroacetyl, trichloroacetyl and trifluoroacetyl.
In another aspect, the present invention provides a process of replacing a thioaryl group with a hydroxyl group according to the scheme
Figure imgf000015_0002
wherein PG is an amine protecting group, An and Ar2 are each aryl groups, where each of An and Ar2 is independently optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbon atoms, and aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon atoms; E is hydrogen or an organic group, and Hg represents a mercury-containing oxidizing agent. Optionaly, PG is benzoyl or tBOC; optionally, E is hydrogen; optionally, An and Ar2 are each phenyl; and optionally Hg is HgO or Hg(CF3CO2)2.
In another aspect, the present invention provides a process of replacing a thioaryl group with a hydroxyl group according to the following scheme
Figure imgf000016_0001
wherein Hg represents a mercuric reagent, and An and Ar2 are independently selected from alkyl, alkenyl, alkynyl, aryl or substituted aryl radical; and R-io is hydrogen, C-i-Cβalkyl, aryl or substituted aryl radical; wherein a substituted aryl radical is substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms. Exemplary mercuric reagents are mercuric oxide and mercuric trifluoroacetate. Optionally, the process is conducted with the addition of eerie ammonium nitrate (CAN).
In another aspect, the present invention provides a process comprising esterifying a compound of the formula
Figure imgf000017_0001
wherein Re is acetyl or dichloroacetyl; and R7 is triethylsilyl, dichloroacetyl or 2,2,2-trichloroethoxycarbonyl (Troc); with an acid compound of a formula selected from
Figure imgf000017_0002
wherein Rs is tBOC, PMP, Bz or H; Rg is thiophenyl, acetoxy, methoxy, t-butoxycarbonyloxy, phenoxy, ethoxyethyl, or dichloroacetyl; and R-io is hydrogen. Optionally, the acid compound has the formula
Figure imgf000017_0003
wherein An is phenyl and Rg is thiophenyl, acetoxy, methoxy, t-butoxycarbonyloxy, phenoxy, ethoxyethyl, or dichloroacetyl. As another option, the acid compound has the formula
Figure imgf000017_0004
wherein An is phenyl, R8 is tBOC, PMP or H, and Rg is acetoxy. As another option, the acid compound has the formula
Figure imgf000018_0001
wherein An is phenyl, R8 is hydrogen or PMP, and R9 is acetoxy, methoxy, t-butoxycarbonyloxy, phenoxy, ethoxyethyl, or dichloroacetyl.
In another aspect, the present invention provides a compound of the formula
Figure imgf000018_0002
wherein Re and R are independently selected from hydrogen, triethylsilyl, acetyl and dichloroacetyl, with the proviso that Re and R7 may not be simultaneously hydrogen, R8 is tBOC, PMP, Bz or H, and Rg is thiophenyl, acetoxy, methoxy, t-butoxycarbonyloxy, ethoxyethyl, or dichloroacetyl.
Optionally, R& and R are each dichloroacetyl; Rs is tBOC; and Rg is thiophenyl, acetoxy, methoxy, t-butoxycarbonyloxy, ethoxyethyl, or dichloroacetyl. As another option, R6 is acetyl, R7 is -TES, R8 is t-BOC, and Rg is thiophenyl, acetoxy, methoxy, t-butoxycarbonyloxy, or dichloroacetoxy. As yet another option, R6 and R7 are each dichloroacetyl, R8 is tBOC, PMP or H, and Rg is acetoxy. One additional option is that R6 is acetyl, R7 is triethylsilyl, R8 is tBOC,
PMP, Bz or H, and Rg is acetoxy, where these options are exemplary options. In another aspect, the present invention provides a process comprising the scheme
Figure imgf000019_0001
wherein R6 and R are independently selected from hydrogen, triethylsilyl, acetyl and dichloroacetyl, with the proviso that Re and R7 may not be simultaneously hydrogen, R8 is tBOC, PMP, Bz or H, and Rg is thiophenyl, acetoxy, methoxy, t-butoxycarbonyloxy, ethoxyethyl, or dichloroacetyl. Optionally, the compound of structure (I) is deprotected at the 2' position to form an intermediate of structure (la), and the intermediate is treated with zinc acetate dihydrate to form the compound of formula (II), where the intermediate has the structure
Figure imgf000019_0002
Also optionally, the compound of formula (I) is treated with protic acid and tertiary amine in an organic solvent to form an intermediate of formula (lb), and the intermediate is deprotected at the 2' position to form the compound of formula (II), where the intermediate has the structure
Figure imgf000020_0001
In another aspect, the present invention provides a method of preparing TAXOTERE, comprising reacting a compound of structure (III) with t- BOC, followed by deprotection of at least one of the 2', 7 and 10 positions, where the compound of structure (III) is
Figure imgf000020_0002
wherein Re and R7 are independently selected from hydrogen, triethylsilyl, acetyl, Troc and dichloroacetyl, with the proviso that Re and R7 may not be simultaneously hydrogen, and R9 is thiophenyl, acetoxy, methoxy, t-butoxycarbonyloxy, or dichloroacetyl or ethoxyethyl. Optionally, R6 and R are each dichloroacetyl and Rg is acetoxy. Also optionally, the compound of structure (III) is prepared by the reduction of a compound of structure (IV)
Figure imgf000021_0001
wherein Re and R are each dichloroacetyl, Rg is acetoxy, and Rn is OCO-t-Bu. In a preferred embodiment, R6 is acetyl or dichloroacetyl, R7 is TES or Troc, and Rg is acetoxy or ethoxyethyl. In one option, the compound of structure (III) is prepared by the reduction of a compound of structure (IV)
Figure imgf000021_0002
wherein R6 is Ac, R7 is TES, Rg is acetoxy, and Rn is PMP, OCOO-t-Bu or H.
In another aspect, the present invention provides a process comprising the scheme
Figure imgf000021_0003
wherein An and Ar2 are independently selected from alkyl, alkenyl, alkynyl, aryl or substituted aryl radical; and R10 is hydrogen, Cι-C6alkyl, aryl or substituted aryl radical; where a substituted aryl radical is substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms. The wavy line from AnS to the ring indicates that both the alpha and beta forms are included.
In another aspect, the present invention provides a process of coupling a beta lactam to a baccatin III compound according to the following scheme
Figure imgf000022_0001
wherein R3 and R are independently selected from hydrogen, hydroxyl, protected hydroxyl, thiol, protected thiol, alkyl, alkenyl, alkynyl, or aryl where R3 and R4 are optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms; R7 is hydroxyl or a protected hydroxyl group; and the coupling is performed by addition of metal hydride, metal alkoxide or lewis acid to the reaction mixture.
In another aspect, the present invention provides a process for making a compound of formulas (III1) or (IV):
Figure imgf000022_0002
Figure imgf000023_0001
comprising the step of reacting a compound of formula (I')
Figure imgf000023_0002
with a compound of formula (lla1) or (lib1)
Figure imgf000023_0003
wherein Ri, R2, R3 and R are independently selected from hydrogen, hydroxyl, protected hydroxyl, thiol, protected thiol, alkyl, alkenyl, alkynyl, or aryl where Ri and R3 are optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms; R = -OCOCHCI2, triethylsilyl or Troc; and R12 is an amine protecting group.
These and other aspects of this invention will be evident upon reference to the following detailed description. BRIEF DESCRIPTION OF THE FIGURES
Figure 1 illustrates several chemical routes for the preparation of beta-lactam and phenylisoserine sidechains according to the present invention.
Figure 2 illustrates a chemical route for the preparation of beta- lactam and phenylisoserine sidechains according to the present invention.
Figure 3 illustrates a chemical route for the preparation of a beta- lactam and phenylisoserine sidechain according to the present invention.
Figure 4 illustrates chemical routes for the preparation of taxotere from various intermediate compounds prepared according to the present invention.
Figure 5 illustrates chemical routes for the preparation of taxotere from various intermediate compound prepared according to the present invention.
DETAILED DESCRIPTION OF THE INVENTION In brief, the present invention relates to 3-phenylisoserine compounds as well as the preparation thereof and the intermediates formed during their preparation; baccatin III compounds and the preparation thereof; methods of joining together a 3-phenylisoserine compound and a baccatin III compound as well as the resulting chemical structure(s); and the conversion of one taxane compound to another taxane compound as well as the resulting chemical structure(s). Before providing a detailed description of these and other aspects of the present invention, the following list of definitions is provided to assist the reader in understanding the invention.
A. Definitions The term "hydroxy-protecting group" refers to a readily cleavable group bonded to the oxygen of a hydroxyl (-OH) group. Examples of hydroxy protecting groups include, without limitation, acetyl (Ac), benzyl (PhCH2), 1- ethoxyethyl (EE), methoxymethyl (MOM), (methoxyethoxy)methyl (MEM), (p- methoxyphenyl)methoxymethyl (MPM), tert-b uty Id i methy Isi ly I (TBS), tert- butyldiphenylsilyl (TBPS), tert-butoxycarbonyl (tBoc, t-Boc, tBOC, t-BOC), tetrahydropyranyl (THP), triphenylmethyl (Trityl, Tr), 2-methoxy-2-methylpropyl, benzyloxycarbonyl (Cbz), trichloroacetyl (OCCCI3), 2,2,2- trichloroethoxycarbonyl (Troc), benzyloxymethyl (BOM), tert-butyl (t-Bu), triethylsilyl (TES), trimethylsilyl (TMS), and triisopropylsilyl (TIPS). The related term "protected hydroxy group" refers to a hydroxy group that is bonded to a hydroxy-protecting group. General examples of protected hydroxy groups include, without limitation, -O-alkyl, -O-acyl, acetal, and -O-ethoxyethyl, where some specific protected hydroxy groups include, formyloxy, acetoxy, propionyloxy, chloroacetoxy, bromoacetoxy, dichloroacetoxy, trichloroacetoxy, trifluoroacetoxy, methoxyacetoxy, phenoxyacetoxy, benzoyloxy, benzoylformoxy, p-nitro benzoyloxy, ethoxycarbonyloxy, methoxycarbonyloxy, propoxycarbonyloxy, 2,2,2-trichloro ethoxycarbonyloxy, benzyloxycarbonyloxy, tert.-butoxycarbonyloxy, 1 -cyclopropyl ethoxycarbonyloxy, phthaloyloxy, butyryloxy, isobutyryloxy, valeryioxy, isovaleryloxy, oxalyoxy, succinyloxy and pivaloyloxy, phenylacetoxy, phenylpropionyloxy, mesyloxy, chlorobenzoyloxy, para-nitrobenzoyloxy, para-tert-butyl benzoyloxy, capryloyloxy, acryloyloxy, methylcarbamoyloxy, phenylcarbamoyloxy, naphthylcarbamoyloxy, and the like. Hydroxy protecting groups and protected hydroxy groups are described in, e.g., C. B. Reese and E. Haslam, "Protective Groups in Organic Chemistry," J. G. W. McOmie, Ed., Plenum Press, New York, N.Y., 1973, Chapters 3 and 4, respectively, and T. W. Greene and P. G. M. Wuts, "Protective Groups in Organic Synthesis," Second Edition, John Wiley and Sons, New York, N.Y., 1991 , Chapters 2 and 3. The term "thiol-protecting group" refers to a readily cleavable group bonded to the sulfur of a thiol (-SH) group. Examples of thiol protecting groups include, without limitation, triphenylmethyl (trityl, Trt), acetamidomethyl (Acm), benzamidomethyl, 1 -ethoxyethyl, benzoyl, and the like. The related term "protected thiol group" refers to a thiol group that is bonded to a thiol- protecting group. General examples of protected thiol groups include, without limitation, -S-alkyl (alkylthio, e.g., Cι-Cιoalkylthio), -S-acyl (acylthio), thioacetal, -S-aralkyl (aralkylthio, e.g., aryl(Cι-C4)alkylthio), where some specific protected thiols groups include methylthio, ethylthio, propylthio, isopropylthio, butylthio, isobutylthio, sec-butylthio, tert-butylthio, pentylthio, isopentylthio, neopentylthio, hexylthio, heptylthio, nonylthio, cyclobutylthio, cyclopentylthio and cyclohexylthio, benzylthio, phenethylthio, propionylthio, n-butyrylthio and iso- butyrylthio. Thio protecting groups and protected thio groups are described in, e.g., C. B. Reese and E. Haslam, "Protective Groups in Organic Chemistry," J. G. W. McOmie, Ed., Plenum Press, New York, N.Y., 1973, Chapters 3 and 4, respectively, and T. W. Greene and P. G. M. Wuts, "Protective Groups in Organic Synthesis," Second Edition, John Wiley and Sons, New York, N.Y., 1991 , Chapters 2 and 3.
The term "amine protecting group" refers to groups known in the art that can be used to protect an amine group from undergoing an undesired chemical reaction. Examples of amine protecting groups include, but are not limited to: acyl types such as formyl, trifluoroacetyl, phthalyl, and p- toluenesulfonyl; aromatic carbamate types such as benzyloxycarbonyl (Cbz) and substituted benzyloxy-carbonyls, 1-(p-biphenyl)-1-methylethoxy-carbonyl, and 9-fluorenylmethyloxycarbonyl (Fmoc); aliphatic carbamate types such as tert-butyloxycarbonyl (tBoc), ethoxycarbonyl, diisopropylmethoxycarbonyl, and allyloxycarbonyl; cyclic alkyl carbamate types such as cyclopentyloxycarbonyl and adamantyloxycarbonyl; alkyl types such as triphenylmethyl and benzyl; trialkylsilane such as trimethylsilane; and thiol containing types such as phenylthiocarbonyl and dithiasuccinoyl. Amine protecting groups and protected amine groups are described in, e.g., C. B. Reese and E. Haslam, "Protective Groups in Organic Chemistry," J. G. W. McOmie, Ed., Plenum Press, New York, N.Y., 1973, Chapters 3 and 4, respectively, and T. W. Greene and P. G. M. Wuts, "Protective Groups in Organic Synthesis," Second Edition, John Wiley and Sons, New York, N.Y., 1991, Chapters 2 and 3. The following Table shows the chemical structure of some protecting groups, as well as nomenclature used to identify those chemical structures.
Figure imgf000027_0001
The term "alkyl" refers to a hydrocarbon structure wherein the carbons are arranged in a linear, branched, or cyclic manner, including combinations thereof. Lower alkyl refers to alkyl groups of from 1 to 5 carbon atoms. Examples of lower alkyl groups include methyl, ethyl, propyl, isopropyl, butyl, s- and t-butyl and the like. Preferred alkyl groups are those of C20 or below. More preferred alkyl groups are those of C13 or below. Cycloalkyl is a subset of alkyl and includes cyclic hydrocarbon groups of from 3 to 13 carbon atoms. Examples of cycloalkyl groups include cyclopropyl, cyclobutyl, cyclopentyl, norbornyl, adamantyl and the like. When an alkyl residue having a specific number of carbons is named, all geometric isomers having that number of carbons are intended to be encompassed; thus, for example, "butyl" is meant to include n-butyl, sec-butyl, isobutyl and t-butyl; "propyl" includes n-propyl and isopropyl.
The term "alkenyl" refers to an alkyl group having at least one site of unsaturation, i.e., at least one double bond.
The term "alkynyl" refers to an alkyl group having at least one triple bond between adjacent carbon atoms. The terms "alkoxy" and "alkoxyl" both refer to moieties of the formula -O-alkyl. Examples include methoxy, ethoxy, propoxy, isopropoxy, cyclopropyloxy, cyclohexyloxy and the like. Lower-alkoxy refers to groups containing one to four carbons. The analogous term "aryloxy" refers to moieties of the formula -O-aryl. The term "acyl" refers to moieties of the formula -C(=O)-alkyl.
One or more carbons in the acyl residue may be replaced by nitrogen, oxygen or sulfur as long as the point of attachment to the parent remains at the carbonyl. Examples include acetyl, benzoyl, propionyl, isobutyryl, t- butoxycarbonyl, benzyloxycarbonyl and the like. Lower-acyl refers to groups containing one to four carbons.
The term aryl refers to phenyl or naphthyl. Substituted aryl refers to mono- and poly- substituted phenyl or naphthyl. Exemplary subsituents for aryl include one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms.
The term "heteroaryl" refers to a 5- or 6-membered heteroaromatic ring containing 1-3 heteroatoms selected from O, N, or S; a bicyclic 9- or 10-membered heteroaromatic ring system containing 0-3 heteroatoms selected from O, N, or S; or a tricyclic 13- or 14-membered heteroaromatic ring system containing 0-3 heteroatoms selected from O, N, or S. Exemplary aromatic heterocyclic rings include, e.g., imidazole, pyridine, indole, thiophene, benzopyranone, thiazole, furan, benzimidazole, quinoline, isoquinoline, quinoxaline, pyrimidine, pyrazine, tetrazole and pyrazole. The term "leaving group" (LG) refer to a chemical moiety that may be displaced during a substitution or elimination reaction. Exemplary leaving groups include halide (e.g., bromide and chloride) and as tosyl.
The term "halogenating agent" refers to a chemical that may be added to a reaction mixture to cause the addition of a halide to a carbon of an organic molecule. Halogenating agents include, for example, inorganic acid halides, for example thionyl chloride, phosphorus trichloride, phosphorus tribromide, phosphoryl chloride trifluoromethanesulfonic acid, N- iodosuccinimide and phosphorus pentachloride. Other halogenating are known in the art. The reaction is conveniently carried out in the presence of an excess of the halogenating agent in the presence of a solvent or diluent such as, for example, a halogenated solvent such as methylene chloride, chloroform or carbon tetrachloride. The reaction may conveniently carried out at a temperature in the range, for example, 10 to 150°C, preferably in the range 40 to 100°C.
In several instances, the present invention provides compounds including the designation "-CO2-E" where E represents hydrogen or an organic group. In these instances, the compounds being disclosed are carboxylic acids or esters thereof. Optionally, E is hydrogen. Alternatively, E is an organic group, where preferred organic groups are alkyl, alkenyl, alkynyl, aryl, or heteroaryl as defined above. Optionally, E has a molecular weight of less than 1 ,000, preferably less than 500 g/mol.
B. Sidechain Preparation
In various aspects, the present invention provides for the preparation of imine compounds, the conversion of an imine compound to a β- lactam compound, the preparation of oxime compounds, the conversion of an oxime compound to a β-lactam, the conversion of one β-lactam compound to another β-lactam compound, the ring-opening of a β-lactam compound to provide a 3-phenylisoserine compound, and the conversion of one 3- phenylisoserine compound to another 3-phenylisoserine compound. These various aspects of the invention are described in detail below. The individual reaction steps, the starting materials and products when novel, and sequences of reaction steps are all aspects of the present invention. 1. Preparation of imine compounds
In one aspect of the invention, as illustrated in Reaction 1 , the reaction of benzaldehyde with anisidine yields a para-methoxyphenyl (PMP)- protected imine.
Reaction 1
Figure imgf000030_0001
More specifically, to a solution of benzaldehyde in an inert solvent such as dichloromethane is added anisidine at about room temperature followed by magnesium sulfate and the reaction mixture stirred at room temperature for about 16 hours. The solid is filtered and the filtrate is evaporated to give the product imine.
In another aspect, the present invention provides a process of forming a beta lactam of the formula
Figure imgf000030_0002
wherein An and Ar2 are each aryl groups, where each of An and Ar2 are independently optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbon atoms, and aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon atoms. The process comprises reacting together compounds of the formula AnS-CH2-C(=O)CI, NH3, and Ar2-CHO under conditions that form the beta lactam. In one embodiment, each of An and Ar2 are phenyl. For example, an aspect of the present invention is illustrated by Reaction 2, wherein an imine may be prepared by reacting benzaldehyde with ammonia.
Reaction 2
Figure imgf000031_0001
More specifically, to a solution of benzaldehyde in a suitable solvent such as ethanol is added ammonia solution at room temperature, and the stirred reaction mixture is heated to about 40-50°C for about 2-3 hours. The resulting solid is filtered and washed with methanol or equivalent followed by water to give the imine.
2. Conversion of an imine compound to a beta-lactam compound
In one aspect, the present invention provides a process of preparing a beta-lactam, comprising the scheme
Figure imgf000031_0002
In this scheme, Ri is hydroxyl, protected hydroxyl, thiol, or protected thiol; LG is a leaving group; R2 is alkyl, alkenyl, alkynyl, or aryl where R2 is optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms; and R3 is hydrogen. In a preferred embodiment, Ri is thioaryl or substituted thioaryl, e.g., thiophenyl or substituted thiophenyl. In one embodiment of the invention, Ri is thiophenyl. In a preferred embodiment, R2 is aryl or substituted aryl, e.g., phenyl or substituted phenyl. In one embodiment of the invention, R2 is phenyl. The scheme shows the formation of the cis product (i.e., Ri and R2 are cis), however it is typically the case that both the cis and trans products are formed. As one option, the imine may be prepared as shown in Reaction 2, wherein (R2)(H)C=N-R3 is prepared by reaction between an aldehyde of the formula R2-CHO, and an amine of the formula R3-NH2.
Reaction 3 shows a specific example of converting an imine to a β-lactam, where this specific conversion is another aspect of the present invention.
Reaction 3
Figure imgf000032_0001
More specifically, an imine is dissolved in an inert solvent such as dichloromethane and cooled to about 0°C under an inert atmosphere such as argon gas. Thiophenyl acetyl chloride or any other respective acid chloride is added dropwise to the cooled stirred solution of the imine at about 0°C. To the resulting solution is added dropwise a tertiary amine, e.g., triethylamine, also at about 0°C. The reaction mixture is gradually warmed to room temperature and kept at this temperature for about 16 hours. The reaction is quenched by pouring into ice-cold water and extracted three times with dichloromethane and dried over anhydrous magnesium sulfate. The solvent is evaporated to give the crude product which is purified by column chromatography using dichloromethane initially followed by mixtures of hexane/ethyl acetate to get the pure cis and trans β-lactams shown in Reaction 3. The cis and trans isomers may be separated from one another by, e.g.,. column chromatography. Either isomer, or the mixture of isomers, may be converted to a phenylisoserine compound as described later herein.
Thus, in another aspect, the present invention also provides compounds of the formula
Figure imgf000032_0002
wherein R^ is thiol (SH), tBOC, acetate, methoxy, thiophenyl, CI2CH-C(O)O- or 1 -ethoxyethyl, R2 is phenyl and R3 is hydrogen.
In another aspect of the invention, an imine without a protecting group attached to the imine nitrogen may be converted to a β-lactam as shown in Reaction 4, where this conversion is another aspect of the invention, and the chemical product is another aspect of the invention.
Reaction 4
Figure imgf000033_0001
More specifically, to a stirred solution of an imine in an inert solvent such as anhydrous dichloromethane, and preferably under an inert atmosphere such as argon gas, is added acetoxy acetyl chloride dropwise at about 0°C. To this solution is added dropwise a tertiary amine, such as triethylamine, also at about 0°C. The reaction mixture is gradually warmed to room temperature and kept at this temperature for overnight. The reaction is quenched by pouring into ice- cold water and extracted three times with dichloromethane following by drying over anhydrous magnesium sulfate. The solvent is evaporated to give the crude product which may be purified by column chromatography using dichloromethane initially followed by mixtures of hexane/ethyl acetate to give the β-lactam.
3. Conversion of an oxime compound to a different oxime compound
In another aspect of the invention, an oxime compound is converted to a protected form as illustrated in Reaction 5.
Reaction 5
Figure imgf000033_0002
More specifically, a syn-benzaldehyde oxime is added to a stirred solution of NaH in anhydrous THF at 0°C under an argon atmosphere. The reaction mixture is stirred at this temperature for 20 minutes and then (BOC)2 is added dropwise. The reaction is stirred at 0°C for 1 hr and worked up as usual. The crude product is purified by column chromatography using hexane/dichloromethane to afford the pure product.
4. Conversion of an oxime compound to a beta-lactam compound
In another aspect the present invention provides a process for preparing a beta lactam, comprising the scheme
Figure imgf000034_0001
wherein Ri is hydroxyl, protected hydroxyl, thiol, or protected thiol; LG is a leaving group; R2 is alkyl, alkenyl, alkynyl or aryl, where R2 may be optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms; and PG is a protecting group. Noteworthy is that this process provides beta-lactam compounds having -O-PG substitution at the heterocyclic nitrogen ring.
As an example, in one aspect of the invention, an oxime compound is converted to a beta-lactam having oxygen substitution on the ring nitrogen, as shown in Reaction 6.
Reaction 6
Figure imgf000034_0002
More specifically, a protected oxime is dissolved in dichloromethane and cooled to 0°C under argon atmosphere. Acetoxy acetyl chloride or any other acid chloride is added dropwise to the cooled stirred solution of the oxime at 0°C. To this solution is added dropwise DMAP or any other base also at 0°C. The reaction mixture is gradually warmed to room temperature (or may be heated to about 40°C) and keep at this temperature for 16 hours. The reaction is quenched by pouring into ice-cold water and extracted three times with dichloromethane and dried over anhydrous magnesium sulfate. The solvent is evaporated to give the crude product which is purified by column chromatography using dichloromethane initially followed by mixtures of hexane/ethyl acetate to get the pure product. Thus, in a related aspect, the present invention provides compounds of the formula
Figure imgf000035_0001
wherein Ri is hydroxyl, protected hydroxyl, thiol, or protected thiol; R2 is alkyl, alkenyl, alkynyl or aryl, where R2 may be optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms; and PG is a protecting group. Optionally, Ri is a protected hydroxyl group and the protecting group is selected from methoxymethyl, methoxyethyl, 1- ethoxyethyl, benzyloxymethyl, (beta-trimethylsilyl-ethoxy)methyl, tetrahydropyranyl, 2,2,2-trichloro-ethoxycarbonyl, benzyloxycarbonyl, tert- butoxycarbonyl, 9-fluorenylmethoxycarbonyl, 2,2,2-trichloroethoxymethyl, trimethylsilyl, triethylsilyl, tripropylsilyl, dimethylethylsilyl, dimethyl(t-butyl)silyl, diethylmethylsilyl, dimethylphenylsilyl, diphenylmethylsilyl, acetyl, chloroacetyl, dichloroacetyl, trichloroacetyl and trifluoroacetyl. Optionally, Ri is a protected thiol group, and the protecting group is selected from triphenylmethyl (trityl, Trt), acetamidomethyl (Acm), benzamidomethyl, 1 -ethoxyethyl and benzoyl. 5. Conversion of a beta-lactam compound to a different beta-lactam compound
A thiophenyl-substituted β-lactam having a protecting group on the ring nitrogen may be deprotected as shown in Reaction 7, where this deprotection reaction is another aspect of the present invention.
Reaction 7
Figure imgf000036_0001
More specifically, cis beta lactam is dissolved in a suitable solvent such as acetonitrile under an inert atmosphere such as argon gas, and cooled to about 0°C. To this stirred cooled solution is added an aqueous solution of eerie ammonium nitrate (CAN) dropwise and the mixture is stirred for about 1 hour. The reaction mixture is poured into water and extracted three times with ethyl acetate. The combined organic phases are successively washed with (a) 5% sodium bicarbonate solution, (b) saturated sodium sulfate solution, and (c) saturated sodium chloride solution, followed by drying over anhydrous sodium sulfite. After evaporation of the solvent under reduced pressure the crude product is purified by column chromatography twice using mixtures of hexane/ethyl acetate and dichloromethane/ethyi acetate to get the pure cis product. The same procedure could also be used to remove the paramethoxy group from trans β-lactam to give the corresponding 3-thiophenyl-azetidinone. In another aspect, the present invention provides a process whereby the nitrogen atom of a beta-lactam is bonded to a protecting group. This aspect of the invention comprises treating a beta lactam of the structure
Figure imgf000036_0002
with a base and a protecting agent, to provide a beta lactam of the structure wherein An and Ar2 are aryl groups independently selected at each occurrence, and R5 is selected from benzoyl and tBOC. The protecting agent may be, for example, benzoyl chloride or di-tert-butyl-dicarbonate. Optionally, this process is proceeded by forming a beta lactam of the formula
Figure imgf000037_0002
by a process comprising reacting together compounds of the formula AnS-CH2- C(=O)CI, base, and Ar2-CHO under conditions that form the beta lactam. The base may be a nitrogen-containing base, e.g., ammonia.
For example, the ring nitrogen of a β-lactam may be protected with an amine protecting group such as benzoyl (Bz, as shown in the following reaction) or t-BOC. This is illustrated in Reaction 8.
Reaction 8
Figure imgf000037_0003
More specifically, a β-lactam is dissolved in an inert solvent such as dichloromethane and cooled to ca. 0°C under an inert atmosphere, e.g., argon gas. Dimethylaminopyridine (DMAP) and triethylamine are added followed by dropwise addition of benzoyl chloride at 0°C with stirring. The reaction mixture is stirred for about 1 hour and then was washed with saturated aqueous ammonium chloride and brine and dried over anhydrous sodium sulfate. After removal of the solvent under reduced pressure the crude product is purified by column chromatography using mixtures of dichloromethane/hexane to afford the pure benzoylated β-lactam.
In another aspect of the invention, a paramethoxyphenyl protecting group attached to the ring nitrogen of a β-lactam is replaced with a benzoyl group as shown in Reaction 9.
Reaction 9
Figure imgf000038_0001
trans
More specifically, the paramethoxy group of the trans β-lactam is removed by using eerie ammonium nitrate (CAN) in aqueous acetonitrile solution, followed by treating the product mixture with benzoyl chloride to afford a mixture of cis and trans benzoylated β-lactams.
In another aspect, the present invention provides for the halogenation of a beta-lactam, as illustrated by the scheme
Figure imgf000038_0002
wherein An and Ar2 are each aryl groups, where each of An and Ar2 is independently optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbon atoms, and aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon atoms; X is halide; R5 is selected from hydrogen, benzoyl and tBOC, and M is a halogenating agent. In one embodiment, each of An and Ar2 is phenyl. Exemplary halogenating agents include, without limitation, inorganic acid halides, for example thionyl chloride, phosphorus trichloride, phosphorus tribromide, phosphoryl chloride trifluoromethanesulfonic acid, N-iodosuccinimide and phosphorus pentachloride. In one embodiment of the invention, the halogenating agent is SO2CI2.
For example, a trans thiophenyl β-lactam can be modified by introducing a chloro group at the 3-position as shown in Reaction 10.
Reaction 10
Figure imgf000039_0001
More specifically, a trans thiophenyl beta lactam is dissolved in an inert solvent, e.g., anhydrous dichloromethane, under an inert atmosphere, e.g., argon gas, and cooled to about 0°C. Sulfuryl chloride is added dropwise to the stirred solution at ca. 0°C and left at this temperature for ca. 2 hrs. The solvent is evaporated and the residue dissolved in dichloromethane and washed successively with water, 10% sodium bicarbonate, saturated brine and dried over anhydrous sodium sulfate. After removal of the solvent under reduced pressure the crude solid is purified by recrystallization using mixtures of diehloromethane/hexanes to give the chloro group at the 3-position of the trans thiophenyl beta lactam.
Thus, the present invention provides compounds of the formula
Figure imgf000039_0002
wherein An and Ar2 are each aryl groups, where each of An and Ar2 are independently optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbon atoms, and aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon atoms; X is halide; and R5 is selected from hydrogen, benzoyl, tBOC, Cι-C6 alkyl or aryl where R5 is optionally substituted with one or more halogens, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms. For example, the invention provides compounds wherein An and Ar2 are each phenyl, X is chloride or bromide; and R5 is hydrogen, benzoyl or tBOC.
In another aspect, the present invention provides a process wherein a halide substituent on a beta-lactam ring is replaced with a protected hydroxyl group, as illustrated by the following scheme
Figure imgf000040_0001
wherein An and Ar2 are each aryl groups, where each of An and Ar2 are independently optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbon atoms, and aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon atoms; M is metal and X is one or more halides attached to the metal; R5 is selected from hydrogen, benzoyl and tBOC; and Re is CI-CΘ alkyl. In one exemplary embodiment of this aspect of the invention, An and Ar2 are each phenyl.
For instance, the present invention provides that a chloro- substituted beta-lactam may be converted into the corresponding beta-lactam where the chloride group is replaced with an acetate group. This conversion is illustrated in Reaction 11. Reaction 11
Figure imgf000041_0001
More specifically, the chloro-substituted beta-lactam is dissolved in an inert solvent, e.g., anhydrous dichloromethane, at room temperature under an inert atmosphere, e.g., argon atmosphere. To this stirred solution at room temperature is added sequentially silica gel, zinc chloride and an alkyl anhydride, e.g., acetic anhydride as shown in reaction XI lb. The reaction mixture is left at this temperature for ca. 16 hrs and then worked up. The silica gel is filtered and the filtrate evaporated, dissolved in dichloromethane and worked up as usual for this type of reaction. The crude residue is purified by column chromatography using mixtures of hexanes/ethyl acetate to afford the pure product.
Thus, the present invention provides compounds of the formula
Figure imgf000041_0002
wherein An and Ar2 are each aryl groups, where each of An and Ar2 are independently optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbon atoms, and aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon atoms; R5 is selected from hydrogen, benzoyl and tBOC; and R9 is a hydroxyl protecting group. For instance, in one aspect Rg is selected from methoxymethyl, methoxyethyl, 1 -ethoxyethyl, benzyloxymethyl, (beta-trimethylsilyl-ethoxy)methyl, tetrahydropyranyl, 2,2,2- trichloro-ethoxycarbonyl, benzyloxycarbonyl, ferf-butoxycarbonyl, 9- fluorenylmethoxycarbonyl, 2,2,2-trichloroethoxymethyl, trimethylsilyl, triethylsilyl, tripropylsilyl, dimethylethylsilyl, dimethyl(t-butyl)silyl, diethylmethylsilyl, dimethylphenylsilyl, diphenylmethylsilyl, acetyl, chloroacetyl, dichloroacetyl, trichloroacetyl and trifluoroacetyl. Alternatively, or in addition, in another aspect An and Ar2 are each phenyl.
In another aspect of the invention, the protecting group of an N- protected beta lactam is replaced with a different protecting group, as shown in Reaction 12.
Reaction 12
Figure imgf000042_0001
More specifically, a paramethoxyphenyl (PMP) group is cleaved by using the procedure as in Reaction 7. The product obtained from this cleavage is dissolved in an inert solvent, e.g., anhydrous dichloromethane, at ca. room temperature under argon atmosphere. To this stirred solution is added DMAP and dropwise benzoyl chloride, and the reaction is maintained at this temperature for about 1.5 hrs. The reaction mixture is worked up as usual and purified by column chromatography using mixtures of hexanes/ethyl acetate to afford the pure benzoylated beta lactam
In another aspect of the invention, the thiophenyl group of a thiophenyl-substituted beta lactam is removed using a desulfurization reagent, and a hydrogen put in its place. An example is shown in Reaction 13, where the desulfurization reagent is Raney Ni.
Reaction 13
Figure imgf000042_0002
In one specific example, a thiophenyl-substituted beta lactam is dissolved in ethanol at room temperature and Raney nickel is added in one portion to the stirred solution and the reaction mixture is stirred at this temperature for about 2 hrs. The reaction mixture is filtered and the filtrate is evaporated. The residue is dissolved in an inert solvent such as dichloromethane and worked up as usual. The crude product is purified by column chromatography using mixtures of hexanes/ethyl acetate to afford the pure product. Often, the product will be obtained as a mixture of N-protected and N-deprotected beta lactams.
In another aspect of the invention, and as illustrated in Reaction 14, a beta lactam with oxygen substitution on the ring nitrogen is converted to the corresponding beta-lactam with hydrogen substitution on the ring nitrogen.
Reaction 14
Figure imgf000043_0001
More specifically, a beta lactam with oxygen substitution on the ring nitrogen is dissolved in methanol at room temperature and treated with Pd(OH)2-C (or any other reducing agent) and the resulting suspension is stirred under hydrogen atmosphere for overnight. The reaction mixture is filtered through a pad of celite and the volatile component(s) of the filtrate are evaporated. The residue was dissolved in dichloromethane and worked up as usual. The crude product is purified by column chromatography using mixtures of hexanes/ethyl acetate to afford the pure beta lactam.
In another aspect, the present invention provides a process comprising the process disclosed in Reaction 15, wherein a thioaryl group is converted to a protected hydroxyl group
Reaction 15
CuOAc
Figure imgf000043_0003
Figure imgf000043_0002
wherein An and Ar2 are independently selected from alkyl, alkenyl, alkynyl, aryl or substituted aryl radical; and R10 is hydrogen, Cι-C6alkyl, aryl or substituted aryl radical; wherein a substituted aryl radical is substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms.
More specifically, a beta lactam with a phenylthio substitution on the ring is dissolved in an organic solvent at room temperature and treated with copper acetate. The reaction mixture is filtered through a pad of celite and the volatile component(s) of the filtrate are evaporated. The crude product is purified by column chromatography using mixtures of hexanes/ethyl acetate to afford the pure beta lactam.
In another aspect, the present invention provides a process comprising the process disclosed in Reaction 16 wherein a thioaryl group is converted to a hydroxyl group
Reaction 16
Figure imgf000044_0001
wherein Hg represents a mercuric reagent, e.g., mercuric oxide or mercuric trifluoroacetate, and An and Ar2 are independently selected from alkyl, alkenyl, alkynyl, aryl or substituted aryl radical; and Rio is hydrogen, Cι-C6alkyl, aryl or substituted aryl radical; wherein a substituted aryl radical is substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms. Optionaly, the mercuric reagent may be combined with eerie ammonium nitrate (CAN). 6. Conversion of a beta-lactam compound to a 3-phenylisoserine compound
In another aspect, the present invention provides a process of opening a beta-lactam ring. The process may be illustrated by the following scheme
Figure imgf000045_0001
wherein Ri is hydroxyl, protected hydroxyl, thiol, or protected thiol; LG is a leaving group; PG is an amino protecting group; R2 is alkyl, alkenyl, alkynyl, or aryl where R2 is optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms; R3 is hydrogen, Cι-C6 alkyl or aryl where R3 is optionally substituted with one or more halogens, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms; and H+ is a proton source. Optionally, the ring- opened product is purified by column chromatography followed by recrystallization, where the recystallization is preferably performed with an organic solvent. The process may be performed in a mixture of organic solvent and aqueous acid. In a preferred embodiment, Ri is thiophenyl, R2 is phenyl, and R3 is hydrogen.
For example, in one embodiment the present invention provides for the conversion of a β-lactam with thiophenyl substitution to the corresponding phenylisoserine compound as shown in Reaction 17. Reaction 17
Figure imgf000046_0001
More specifically, a β-lactam is dissolved in a minimum volume of DMSO or mixtures of DMSO/DCM and hydrochloric acid is added. The stirred reaction mixture is heated to about 85°C for ca. 16 hrs. The reaction mixture is cooled to room temperature and dried under vacuum to give a powder, which is the salt of an intermediate compound of the structure
Figure imgf000046_0002
This powder is dissolved in pyridine under an inert atmosphere (e.g., argon) and benzoyl chloride is added dropwise at room temperature. The reaction mixture is stirred at this temperature for about 2 hrs. The reaction mixture is acidified with 0.1N HCI and the crude product is extracted with dichloromethane. The combined organic extracts are dried over anhydrous magnesium sulfate and concentrated in vacuo to dryness. The crude product is purified by column chromatography using hexane/ethyl acetate and dichloromethane/ methanol to afford the pure cis phenylisoserine side chain.
In another aspect of the invention, ring-opening of a β-lactam provides a phenylisoserine compound as illustrated in Reaction 18.
Reaction 18
Figure imgf000046_0003
More specifically, treatment of a trans β-lactam with protic acid followed by reaction with benzoyl chloride in base (e.g., pyridine) affords a trans phenylisoserine side chain. In another aspect, the present invention provides a process wherein a beta-lactam having both thiophenyl and protected hydroxyl substitution is converted to a ring-opened form, as illustrated by the following scheme
Figure imgf000047_0001
wherein An and Ar2 are aryl groups independently selected at each occurrence, R5 is selected from hydrogen, benzoyl and tBOC, R6 is a hydroxy protecting group, and R7 is hydrogen or Ci-Cealkyl, where R as Cι-C6alkyl is introduced in an optional esterification reaction. H+ represents a proton source, e.g., mineral acid or organic acid. In one aspect of the invention, An and Ar2 are each phenyl.
In a separate aspect, the present invention provides a process of opening a beta lactam according to the scheme
Figure imgf000047_0002
wherein PG is a hydroxyl protecting group; An and Ar2 are each aryl groups, where each of An and Ar2 are independently optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbon atoms, and aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon atoms; and Ri is hydrogen, alkyl, or -O-PG wherein PG is a protecting group.
For example, in one aspect of the invention, a beta-lactam is ring- opened to afford the corresponding phenylisoserine compound as shown in Reaction 19. Reaction 19
Figure imgf000048_0001
More specifically, the paramethoxyphenyl (PMP) group of the beta-lactam shown in Reaction 19 is cleaved by using the procedure as in Reaction 7. The product obtained from this cleavage is dissolved in a minimum volume of dichloromethane at room temperature and a solution of hydrochloric acid is added. The stirred solution is heated to about 60°C for about 3 hrs. The reaction mixture is cooled to room temperature and concentrated in vacuo to dryness, giving the acid as a powder.
In another aspect, the present invention provides a process whereby a beta lactam having oxygen substitution on the ring nitrogen is converted into a phenylisoserine compound, as illustrated in Reaction 20.
Reaction 20
Figure imgf000048_0002
More specifically, a beta lactam having oxygen substitution on the ring nitrogen is dissolved in dichloromethane at room temperature under argon atmosphere and TMSCI is added. This solution is stirred for about 4 hrs and worked up as usual. The combined organic extracts are dried over anhydrous magnesium sulfate and concentrated in vacuo to dryness to give a solid product. Thus, the present invention generally provides isoserine compound of the formula
Figure imgf000048_0003
, _ . ,,, 004/033442
wherein Ri is hydroxyl, protected hydroxyl, thiol, or protected thiol; PG is an amino protecting group; R2 is alkyl, alkenyl, alkynyl, or aryl where R2 is optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms; R3 is hydrogen, Cι-C6 alkyl or aryl where R3 is optionally substituted with one or more halogens, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms; and salts and esters thereof. In one aspect, the isoserine compound is characterized by having Ri be hydroxyl or protected hydroxyl; R2 be aryl; and R3 be hydrogen; including salts and esters thereof. In another aspect, the isoserine compound is characterized by having Ri be thiol or protected thiol; R be aryl; R3 be hydrogen; and includes salts and esters thereof.
In addition, the present invention provides compounds of the formula
Figure imgf000049_0001
wherein An and Ar2 are aryl groups independently selected at each occurrence, R5 is selected from hydrogen, benzoyl and tBOC, R is a hydroxyl protecting group, and R is hydrogen or CrCβalkyl. Optionally, Re is selected from methoxymethyl, methoxyethyl, 1 -ethoxyethyl, benzyloxymethyl, (beta- trimethylsilyl-ethoxy)methyl, tetrahydropyranyl, 2,2,2-trichloro-ethoxycarbonyl, benzyloxycarbonyl, fetf-butoxycarbonyl, 9-fluorenylmethoxycarbonyl, 2,2,2- trichloroethoxymethyl, trimethylsilyl, triethylsilyl, tripropylsilyl, dimethylethylsilyl, dimethyl(t-butyl)silyl, diethylmethylsilyl, dimethylphenylsilyl, diphenylmethylsilyl, acetyl, chloroacetyl, dichloroacetyl, trichloroacetyl and trifluoroacetyl. Furthermore, the present invention provides isoserine compounds of the formula
Figure imgf000050_0001
wherein Ar2 is an aryl group R5 is selected from hydrogen, benzoyl and tBOC, R6 is a thiol protecting group, and R7 is H or Cι-C6 alkyl. Optionally, the thiol protecting group is triphenylmethyl (trityl, Trt), acetamidomethyl (Acm), benzamidomethyl, 1 -ethoxyethyl or benzoyl.
7. Conversion of a 3-phenylisoserine compound to another 3- phenylisoserine compound In one aspect, the present invention provides a process whereby a thioaryl group in a phenylisoserine compound is replaced with a hydroxyl group, as shown in the following Reaction 21.
Reaction 21
Figure imgf000050_0002
In Reaction 21 , PG is an amine protecting group, An and Ar2 are aryl groups, E is hydrogen or an organic group, and Hg represents a mercury-containing oxidizing agent. Optionally, PG is benzoyl or tBOC, and/or E is hydrogen, and/or An is phenyl, and/or Ar2 is phenyl. Two exemplary mercuric oxidizing agents are HgO and Hg(CF3CO2)2. For example, the present invention provides that a thiophenyl group located at the 2-position of a 3-phenylisoserine may be replaced with a hydroxyl group of the opposite configuration, as shown in Reaction 22. Reaction 22
Figure imgf000051_0001
More specifically, a trans 2-thiophenyl 3-phenylisoserine compound is dissolved in an inert solvent, e.g., freshly distilled THF, under an inert atmosphere, e.g., argon gas, and a mercury-containing oxidizing agent, e.g., mercuric oxide (HgO) or Hg(CF3CO2)2 as shown in Reaction 22, is added in one portion at room temperature and the reaction mixture stirred at this temperature for about 72 hrs. The reaction is worked up according to procedures known in the art for reactions with mercuric oxidizing agent, and the product is purified by column chromatography using mixtures of acetone/methanol to afford the pure cis phenylisoserine side chain.
In another aspect, the present invention provides a process whereby a hydroxyl group in a phenylisoserine compound is converted to a protected hydroxyl group, as shown in Reaction 23.
Reaction 23
In Reaction 23, PGi is an amine protecting group, An and Ar2 are aryl groups, E is hydrogen or an organic group, PG2 is a hydroxyl protecting group, and PG2-X represents a reagent that introduces a protecting group onto a hydroxyl group. Optionally, PGi is benzoyl or tBOC, and/or E is hydrogen, and/or An is phenyl, and/or Ar2 is phenyl and/or PG2 is acetyl. An exemplary reagent to add a protecting group onto a hydroxyl group is acetyl chloride. Other reagents are well known in the art, including those set forth in T. W. Greene and P. G. M. Wuts, "Protective Groups in Organic Synthesis," Second Edition, John Wiley and Sons, New York, N.Y., 1991, Chapters 2 and 3. For example, the present invention provides for the acylation of the 2-hydroxy group of a 3-phenyl-2-hydroxy isoserine compound, as shown in Reaction 24.
Reaction 24
Figure imgf000052_0001
More specifically, a cis phenylisoserine compound is dissolved in a basic solvent, e.g., pyridine, under an inert atmosphere, e.g., argon gas, at about room temperature and acetyl chloride is added dropwise to the stirred solution. The solution is stirred for about 30 minutes and worked up according to methods known in the art for acylation reaction. The crude product is purified by column chromatography using mixtures of dichloromethane/methanol to afford the pure acetylated cis phenylisoserine side chain acid.
In another aspect, the present invention provides a process whereby a thioaryl group is removed from an arylisoserine compound, as illustrated by the scheme
Figure imgf000052_0002
wherein An and Ar2 are aryl groups independently selected at each occurrence, R5 is selected from hydrogen, benzoyl and tBOC, Re is Cι-C6 alkyl, R7 is H or Cι-C6 alkyl, and E represents a desulfuration reagent. Raney nickel is a suitable desulfurization reagent. In a preferred embodiment, each of An and Ar2 is phenyl. For example, the present invention provides a process whereby a thioaryl group is removed from an arylisoserine compound as illustrated by the scheme of Reaction 25. Reaction 25
Figure imgf000053_0001
In the above scheme, An and Ar2 are aryl groups, E is hydrogen or an organic group, and OPG represents a protected hydroxyl group. Optionally, An is phenyl, and/or Ar2 is phenyl, and/or E is hydrogen and/or PG is acetyl or ethoxyethyl (EE).
Thus, the present invention provides compounds of the formula
NHR5 o
OR6
wherein Ar2 is an aryl group R5 is selected from hydrogen, benzoyl and tBOC, R6 is a hydroxyl protecting group, and R is H or Cι-C6 alkyl. Optionally, R6 is selected from methoxymethyl, methoxyethyl, 1 -ethoxyethyl, benzyloxymethyl, (beta-trimethylsilyl-ethoxy)methyl, tetrahydropyranyl, 2,2,2-trichloro- ethoxycarbonyl, benzyloxycarbonyl, te/f-butoxycarbonyl, 9- fluorenylmethoxycarbonyl, 2,2,2-trichloroethoxymethyl, trimethylsilyl, triethylsilyl, tripropylsilyl, dimethylethylsilyl, dimethyl(t-butyl)silyl, diethylmethylsilyl, dimethylphenylsilyl, diphenylmethylsilyl, acetyl, chloroacetyl, dichloroacetyl, trichloroacetyl and trifluoroacetyl.
In another aspect, the present invention provides a process whereby a protecting group is added to the amino group of an arylisoserine compound, as illustrated in the scheme of Reaction 26. Reaction 26
Figure imgf000054_0001
In Reaction 26, An and Ar2 are aryl groups, E is hydrogen or an organic group, PGi represents a hydroxyl protecting group and PG2 represents an amine protecting group. Optionally, An is phenyl, and/or Ar2 is phenyl, and/or E is hydrogen and/or PGi is acetyl. Optionally, when paclitaxel is the target taxane, PG2 is a benzoyl group. However, when taxotere is the target taxane, then PG2 is a tBOC group.
In another aspect of the present invention, a protecting group is added to the amine group of a 3-arylisoserine compound, and a thioaryl group is removed from the alpha carbon, as illustrated in Reaction 27, where phenyl is shown as a representative aryl group, acetate is shown as a representative hydroxyl protecting group, and benzoyl is shown as a representative amine protecting group.
Reaction 27
OH
Figure imgf000054_0002
More specifically, a phenylisoserine compound is dissolved in ethanol at room temperature and Raney nickel is added in one portion to the stirred solution and the reaction mixture is stirred at this temperature for 3 hrs. The reaction mixture is filtered and the filtrate is evaporated. The residue is dissolved in dichloromethane and worked up as usual. This resulting solid is dissolved in pyridine under argon atmosphere and benzoyl chloride added dropwise at room temperature. The reaction mixture is stirred at this temperature for about 4 hrs. The reaction mixture is acidified with 0.1N HCI and the crude product is extracted with dichloromethane. The combined organic extracts are dried over anhydrous magnesium sulfate and concentrated in vacuo to dryness. The crude product is purified by column chromatography using dichloromethane/methanol to afford the pure cis 2'-acetylated phenylisoserine side chain. When taxotere is the target taxane, a reagent that adds a tBOC group to an amine group may be used in lieu of benzoyl chloride.
In another aspect of the invention, the protecting group on the nitrogen atom of a 3-phenylisoserine compound is replaced with a different protecting group as illustrated in Reaction 28.
Reaction 28
Figure imgf000055_0001
Here, a O-t-BOC protected phenylisoserine compound is treated under reducing conditions as shown in reaction 28, and then benzoylated using benzoyl chloride in pyridine according to reaction 27 to give the 2'-protected phenylisoserine taxol side chain.
8. Combinations of Reactions
The various reactions described in this section may be carried out sequentially, so long as the product of one reaction may be used as the starting material of another reaction. Each of these possible combinations is a separate aspect of the present invention. Exemplary reaction sequences are shown in Figures 1-3.
C. Baccatin III Compounds
C7-dichloroacetyl baccatin III
In one aspect the present invention provides C7-dichloroacetyl baccatin III of the following formula (R7 = -OCOCHCI2).
Figure imgf000056_0001
This compound is a useful intermediate in the production of taxanes. This compound may be prepared according to Reaction 29, which is another aspect of the present invention.
Reaction 29
Figure imgf000056_0002
In Reaction 29, the base may be an amine base, e.g., dimethylaminopyridine (DMAP). The reaction is typically conducted in an inert solvent, e.g., dichloromethane (DCM). For example, Baccatin III may be dissolved in anhydrous dichloromethane under an argon atmosphere at room temperature. To this solution is added DMAP followed by dichloroacetyl chloride. The mixture is left at room temperature for overnight. The mixture is then quenched with cold water and extracted thrice with dichloromethane. The organic layer is washed with water and than with brine to remove unwanted salts. The organic layer may then be dried and evaporated under vacuum, and the residue recrystallized or column chromatographed with dichloromethane/ethyl acetate mixtures to afford C7 protected baccatin III.
Alternatively, the C7 protected baccatin III or C7 and C10 protected baccatin III can also be prepared from 10 DAB or 9DHB (9-dihydro- 13-acetylbaccatin III) in a similar manner. C7-triethylsilyl baccatin III
In one aspect the present invention provides C7-triethylsilyl baccatin III of the following formula (R7 = -O-Si(CH2CH3)3).
Figure imgf000057_0001
This compound is a useful intermediate in the production of taxanes. This compound may be prepared according to Reaction 30, which is another aspect of the present invention.
Reaction 30
Figure imgf000057_0002
In Reaction 30, the base may be an amine base, e.g., dimethylaminopyridine (DMAP) or pyridine. The reaction is typically conducted in an inert solvent, e.g., dichloromethane (DCM). For example, Baccatin III may be dissolved in anhydrous dichloromethane under an argon atmosphere at room temperature. To this solution is added pyridine followed by triethylsilyl chloride. The mixture is left at room temperature for overnight. The mixture is then quenched with cold water and extracted thrice with dichloromethane. The organic layer is washed with water and than with brine to remove unwanted salts. The organic layer may then be dried and evaporated under vacuum, and the residue recrystallized or column chromatographed with dichloromethane/ethyl acetate mixtures to afford C7 protected baccatin III. D. Condensation of the C7 Protected Baccatin III with the Side Chain
In another aspect, the present invention provides for the coupling of a sidechain as described in the previous section, which may be either a beta lactam or a phenylisoserine, with a baccatin-type compound. In general, the baccatin-type compound is described by the formula
Figure imgf000058_0001
wherein Re and R are selected from hydrogen and hydroxy protecting groups. The sidechain couples to the baccatin-type compound at the hydroxyl group located at C13 of the baccatin-type compound. In various exemplary embodiments of the invention: Re is acetyl and R is tnethylsily (TES); R6 is acetyl and R is -COCHCI2; R6 is dichloroacetyl and R is tnethylsily (TES); or Re is dichloroacetyl and R7 is -COCHCI2. In a preferred embodiment, the coupling is performed in the presence of a dialkylcarbodiimide, e.g., dicyclohexylcarbodiimide. In one embodiment, a di-chloroacetyl baccatin III (R7 = -
OCOCHCI2) or triethylsilyl (TES) baccatin III (R7 = TES) of the following formula (I"):
Figure imgf000058_0002
is reacted with an N-CBz C2'-protected 3-phenylisoserine side chain of the following formula (lla"), or with a β-lactam of the following formula (Mb"):
Figure imgf000059_0001
(lla") (lib")
to form an intermediate of the following formulas (III") or (IV):
Figure imgf000059_0002
Figure imgf000059_0003
In another embodiment, the intermediate of formula (III") or (IV") is further modified to yield paclitaxel or analogs thereof. For example, the R group at the C7 position and the R group at the C2' site may be converted to hydroxyl groups to yield paclitaxel. In one embodiment of the invention, these coupling reactions are accomplished under the influence of a dialkylcarbodiimide, e.g., DCC.
In general, reaction of a beta lactam (see, e.g., Reactions 6, 8, 9, 12, and 13) or a phenylisoserine side chain (see, e.g., Reactions 10, 11 , 18, 20, 22 and 24) may be accomplished by reacting with a C7 protected baccatin III (Schemes I and II below) to yield an intermediate of the following formula (Ilia") or (1Mb") or (IVa") or (IVbM):
Figure imgf000060_0001
wherein R is acetyl, R7 is a hydroxy protecting group, and Re is benzoyl (compound Ilia") or t-BOC (compound lllb"); and
Figure imgf000060_0002
wherein R is acetyl, R7 is a hydroxy protecting group, and R8 is benzoyl (compound IVa") or t-BOC (compound IVb").
Such reaction between compounds of formulas (I") and those of formulas (lla") and (Mb") may be accomplished as illustrated in following reaction Schemes.
Scheme 1
Figure imgf000060_0003
R 7 = OTES or OCOCHCl 2
C7 protected baccatin HI Here, the side chain acid of formula lla" (obtained as described previously) is dissolved in anhydrous toluene under argon atmosphere at room temperature. To this stirred solution of the side chain acid is added sequentially DCC, DMAP and the C7 protected baccatin III of formula I". The resulting mixture is then heated at about 75°C for 16 hrs. It should be noted that any other dialkycarbodiimides may be substituted for the dicyclohexylcarbodiimide (DCC), with one example being diisopropylcarbodiimide. The solution is then allowed to cool to room temperature, and next an equal volume of dichloromethane is added. The combined organics are then washed with cold dilute hydrochloric acid solution, water, and finally brine. The organic layer is separated, dried, and reduced under vacuum. The resulting residue is purified by column chromatography using mixtures of dichloromethane/ethyl acetate or hexanes/ethyl acetate to afford the pure coupled intermediate taxane of formula III" or IV". The process illustrated by Scheme 1 is suited for the preparation of paclitaxel since the sidechain amino group is protected with a benzoyl group. In another embodiment of the invention (not illustrated) the process of Scheme 1 is performed with a sidechain having a t-BOC protecting group for the sidechain amino group, where this embodiment is well-suited for the preparation of taxotere.
Scheme 2
Figure imgf000061_0001
In Scheme 2, in preferred embodiments, R3 is H, SPh, OH, OAc or ethoxyethyl, R4 is H or SPh, and R7 is O-TES or OCOCHCI2. Here, the beta lactam of formula lib" (obtained as described previously) and the C7 protected baccatin III is dissolved in anhydrous freshly distilled THF under argon atmosphere at room temperature. This stirred solution is cooled to 0°C and added to a suspension of NaH in THF at 0°C. The solution is warmed slowly to room temperature and maintained at this temperature for 3 hrs. The reaction mixture was cooled to 0°C and quenched with brine. The reaction mixture was extracted with dichloromethane and the combined extracts were washed several times with brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to give the crude product. The crude product was purified by column chromatography using mixtures of hexanes/ethyl acetate to afford the pure coupled intermediate taxane of formula III" or IV" that could be converted to taxol or its analogs. Although this reaction is illustrated with sodium hydride, in other aspects of the invention the coupling is performed in the presence of a metal base salts, e.g., a metal hexamethyldisilazide (e.g., LiHMDS, NaHMDS, KHMDS), or a Lewis acid, e.g., boron trifluoride etherate.
The process illustrated by Scheme 2 is suited for the preparation of paclitaxel since the nitrogen atom of the beta-lactam is protected with a benzoyl (Bz) group. In another embodiment of the invention (not illustrated) the process of Scheme 2 is performed with the nitrogen atom of the beta-lactam being protected by a t-BOC protecting group, where this embodiment is well- suited for the preparation of taxotere.
Additional examples of the coupling of a sidechain to a baccatin- type compound are shown in the following Schemes 3 and 4. Each of Schemes 3 and 4 is a separate aspect of the present invention. In these schemes "R" represents hydrogen or an organic group, e.g., R may be hydroxyl, protected hydroxyl, thiol, or protected thiol; alternatively R may be alkyl, alkenyl, alkynyl or aryl, where R may be optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms. Preferably, "R" is selected as appropriate for the preparation of paclitaxel or taxotere. DCC is shown as the coupling reagent in Schemes 3 and 4 for illustrative purpoes, however, other dialkylcarbodiimides may be used in lieu of, or in combination with, dicyclohexylcarbodiimide (DCC). Scheme 3
Figure imgf000063_0001
C7, C10-bis(dichIoroacetyl)10DAB
Figure imgf000063_0002
C7, triethylsilyl baccatin III
Scheme 4
Figure imgf000064_0001
C7, C10-bis(dichloroacetyl)10DAB
II
Figure imgf000064_0002
C7, triethylsilyl baccatin III
E. Conversion of the compound of formula III or IV to paclitaxel, taxotere, or an analog thereof Following synthesis of compounds of formula III" or IV", the same may then be used as an intermediate for the preparation of paclitaxel, taxotere, or analogs thereof. For example, the following Scheme 5 illustrates hydrolysis of the C2'-protected groups and C7-dichloroacetyl or TES to form paclitaxel under mild conditions, thus not disturbing the ester linkage and various substituents. Scheme 5
Figure imgf000065_0001
R3 = H or SPh or OH or OAc
R4= H or SPh
R7= OTES or OCOCHCl2
Figure imgf000065_0002
R, = H or SPh or OH or OAc
R2= H or SPh
R7= OTES or OCOCHCl2
Here, the C2' protected groups and the C7 protected groups can be removed to give taxol or its analogs. An analogous process of the present invention for the preparation of taxotere is shown in Figures 4 and 5.
All of the above U.S. patents, U.S. patent application publications, U.S. patent applications, foreign patents, foreign patent applications and non- patent publications referred to in this specification and/or listed in the Application Data Sheet, are incorporated herein by reference, in their entirety.
From the foregoing it will be appreciated that, although specific embodiments of the invention have been described herein for purposes of illustration, various modifications may be made without deviating from the spirit and scope of the invention. Accordingly, the invention is not limited except as by the appended claims.

Claims

What I claim is:
1. A process of preparing a beta-lactam, comprising the scheme
Figure imgf000067_0001
wherein
Ri is hydroxyl, protected hydroxyl, thiol, or protected thiol;
LG is a leaving group;
R2 is alkyl, alkenyl, alkynyl, or aryl where R2 is optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms; and
R3 is hydrogen.
2. The process of claim 1 wherein (R2)(H)C=N-R3 is prepared by reaction between an aldehyde of the formula R2-CHO, and an amine of the formula R3-NH2.
3. The process of claim 1 conducted in a chlorinated solvent.
The process of claim 1 wherein Ri is phenyl and R2 is phenyl.
5. A compound of the formula
Figure imgf000068_0001
wherein Ri is thiol (SH), tBOC, acetate, methoxy, thiophenyl, CI2CH-C(O)O- or 1 -ethoxyethyl, R2 is phenyl and R3 is hydrogen.
6. A compound of claim 5 wherein R1 is thiophenyl.
A process of opening a beta-lactam ring, comprising the scheme
Figure imgf000068_0002
wherein
Ri is hydroxyl, protected hydroxyl, thiol, or protected thiol;
LG is a leaving group;
PG is an amino protecting group;
R2 is alkyl, alkenyl, alkynyl, or aryl where R2 is optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms;
R3 is hydrogen, CrC6 alkyl or aryl where R3 is optionally substituted with one or more halogens, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms; and
H+ is a proton source.
8. The process of claim 7 wherein the beta-lactam was prepared by the process of claim 1.
9. The process of claim 7 wherein the beta-lactam was prepared by the process of claim 2.
10. The process of claim 7 wherein the ring-opened product is purified by column chromatography followed by recrystallization.
11. The process of claim 10 wherein recystallization is performed with an organic solvent.
12. The process of claim 7 conducted in a mixture of organic solvent and aqueous acid.
13. The process of claim 7 wherein R-i is thiophenyl, R2 is phenyl, and R3 is hydrogen.
14. An isoserine compound of the formula
PG. .R3
*N O
Ri
wherein
Ri is hydroxyl, protected hydroxyl, thiol, or protected thiol; PG is an amino protecting group;
R2 is alkyl, alkenyl, alkynyl, or aryl where R2 is optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms;
R3 is hydrogen, Cι-C6 alkyl or aryl where R3 is optionally substituted with one or more halogens, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms; and salts and esters thereof.
15. An isoserine compound of claim 14, wherein Ri is hydroxyl or protected hydroxyl;
R2 is aryl;
R3 is hydrogen; and salts and esters thereof.
16. An isoserine compound of claim 14, wherein Ri is thiol or protected thiol;
R2 is aryl;
R3 is hydrogen; and salts and esters thereof.
17. A process of forming a beta lactam of the formula
Figure imgf000070_0001
wherein An and Ar2 are each aryl groups, where each of An and Ar2 are independently optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbon atoms, and aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon atoms; comprising reacting together compounds of the formula Ar-|S-CH2- C(=O)CI, NH3, and Ar2-CHO under conditions that form the beta lactam.
18. The process of claim 17 wherein each of An and Ar2 are phenyl.
19. A process comprising the scheme
Figure imgf000071_0001
wherein Aη and Ar2 are each aryl groups, where each of Aη and Ar2 is independently optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbon atoms, and aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon atoms; X is halide; R5 is selected from hydrogen, benzoyl and tBOC, and M is a halogenating agent.
20. The process of claim 19 wherein each of Aη and Ar2 is phenyl.
21. The process of claim 19 wherein the halogenating agent is
SO2CI2.
22. A compound of the formula
Figure imgf000071_0002
wherein
An and Ar2 are each aryl groups, where each of Ar-i and Ar2 are independently optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbon atoms, and aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon atoms;
X is halide; and
Rs is selected from hydrogen, benzoyl, tBOC, Cι-C6 alkyl or aryl where R5 is optionally substituted with one or more halogens, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms.
23. A compound of claim 22 wherein An and Ar2 are each phenyl, X is chloride or bromide; and R5 is hydrogen, benzoyl or tBOC.
24. A process comprising the scheme
Figure imgf000072_0001
wherein
An and Ar2 are each aryl groups, where each of An and Ar2 are independently optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbon atoms, and aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon atoms; M is metal and X is one or more halides attached to the metal; Rs is selected from hydrogen, benzoyl and tBOC; and Re is C Ce alkyl.
25. The process of claim 24 wherein A and Ar2 are each phenyl.
26. A compound of the formula
Figure imgf000073_0001
wherein
An and Ar2 are each aryl groups, where each of An and Ar2 are independently optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbon atoms, and aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon atoms;
Rs is selected from hydrogen, benzoyl and tBOC; and
Rg is a hydroxyl protecting group.
27. The compound of claim 26 wherein Rg is selected from methoxymethyl, methoxyethyl, 1 -ethoxyethyl, benzyloxymethyl, (beta- trimethylsilyl-ethoxy)methyl, tetrahydropyranyl, 2,2,2-trichIoro-ethoxycarbonyl, benzyloxycarbonyl, ferf-butoxycarbonyl, 9-fluorenylmethoxycarbonyl, 2,2,2- trichloroethoxymethyl, trimethylsilyl, triethylsilyl, tripropylsilyl, dimethylethylsilyl, dimethyl(t-butyl)silyl, diethylmethylsilyl, dimethylphenylsilyl, diphenylmethylsilyl, acetyl, chloroacetyl, dichloroacetyl, trichloroacetyl and trifluoroacetyl.
28. The compound of claim 26 wherein An and Ar2 are each phenyl.
29. A process comprising the scheme
Figure imgf000074_0001
wherein An and Ar2 are aryl groups independently selected at each occurrence, R5 is selected from hydrogen, benzoyl and tBOC, R6 is a hydroxy protecting group, and R7 is hydrogen or Cι-C6alkyl.
30. The process of claim 29 wherein An and Ar2 are each phenyl.
31. A process of opening a beta lactam according to the scheme
Figure imgf000074_0002
wherein
PG is a hydroxyl protecting group;
An and Ar2 are each aryl groups, where each of An and Ar2 are independently optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbon atoms, and aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon atoms;
Ri is hydrogen, alkyl, or -O-PG wherein PG is a protecting group.
32. A compound of the formula
Figure imgf000075_0001
wherein An and Ar2 are aryl groups independently selected at each occurrence, Rs is selected from hydrogen, benzoyl and tBOC, Re is a hydroxyl protecting group, and R is hydrogen or Cι-C6alkyl.
33. The compound of claim 32 wherein Re is selected from methoxymethyl, methoxyethyl, 1 -ethoxyethyl, benzyloxymethyl, (beta- trimethylsilyl-ethoxy)methyl, tetrahydropyranyl, 2,2,2-trichloro-ethoxycarbonyl, benzyloxycarbonyl, tetf-butoxycarbonyl, 9-fluorenylmethoxycarbonyl, 2,2,2- trichloroethoxymethyl, trimethylsilyl, triethylsilyl, tripropylsilyl, dimethylethylsilyl, dimethyl(t-butyl)silyl, diethylmethylsilyl, dimethylphenylsilyl, diphenylmethylsilyl, acetyl, chloroacetyl, dichloroacetyl, trichloroacetyl and trifluoroacetyl.
34. A process comprising the scheme
Figure imgf000075_0002
wherein An and Ar2 are aryl groups independently selected at each occurrence, Rs is selected from hydrogen, benzoyl and tBOC, R6 is Cι-C6 alkyl, R7 is H or Ci-Cβ alkyl, and E represents a desulfuration reagent.
35. A compound of the formula
NHR5 O
OR6
wherein Ar2 is an aryl group R5 is selected from hydrogen, benzoyl and tBOC, R6 is a hydroxyl protecting group, and R is H or Cι-C6 alkyl.
36. The compound of claim 35 wherein Re is selected from methoxymethyl, methoxyethyl, 1 -ethoxyethyl, benzyloxymethyl, (beta- trimethylsilyl-ethoxy)methyl, tetrahydropyranyl, 2,2,2-trichloro-ethoxycarbonyl, benzyloxycarbonyl, tetf-butoxycarbonyl, 9-fluorenylmethoxycarbonyl, 2,2,2- trichloroethoxymethyl, trimethylsilyl, triethylsilyl, tripropylsilyl, dimethylethylsilyl, dimethyl(t-butyl)silyl, diethylmethylsilyl, dimethylphenylsilyl, diphenylmethylsilyl, acetyl, chloroacetyl, dichloroacetyl, trichloroacetyl and trifluoroacetyl.
37. A compound of the formula
Figure imgf000076_0001
wherein Ar2 is an aryl group R5 is selected from hydrogen, benzoyl and tBOC, Re is a thiol protecting group, and R7 is H or Cι-C6 alkyl.
38. The compound of claim 37 wherein the thiol protecting group is triphenylmethyl (trityl, Trt), acetamidomethyl (Acm), benzamidomethyl, 1 -ethoxyethyl or benzoyl.
39. A process of substituting the nitrogen of a beta lactam, comprising treating a beta lactam of the structure
Figure imgf000077_0001
with a base and a protecting agent, to provide a beta lactam of the structure
Figure imgf000077_0002
wherein An and Ar2 are aryl groups independently selected at each occurrence, and R5 is selected from benzoyl and tBOC.
40. The process of claim 39 wherein the protecting agent is benzoyl chloride or di-tert-butyl-dicarbonate
41. The process of claim 39 proceeded by forming a beta lactam of the formula
Figure imgf000077_0003
by a process comprising reacting together compounds of the formula AnS-CH2- C(=O)CI, base, and Ar2-CHO under conditions that form the beta lactam.
42. The process of claim 41 wherein the base is ammonia.
43. A process for preparing a beta lactam, comprising the scheme
Figure imgf000078_0001
wherein
Ri is hydroxyl, protected hydroxyl, thiol, or protected thiol;
LG is a leaving group;
R2 is alkyl, alkenyl, alkynyl or aryl, where R2 may be optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms; and
PG is a protecting group.
44. A compound of the formula
Figure imgf000078_0002
Ri is hydroxyl, protected hydroxyl, thiol, or protected thiol;
R2 is alkyl, alkenyl, alkynyl or aryl, where R2 may be optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms; and
PG is a protecting group.
45. The compound of claim 44 wherein R-i is a protected hydroxyl group and the protecting group is selected from methoxymethyl, methoxyethyl, 1 -ethoxyethyl, benzyloxymethyl, (beta-trimethylsilyl- ethoxy)methyl, tetrahydropyranyl, 2,2,2-trichloro-ethoxycarbonyl, benzyloxycarbonyl, fetf-butoxycarbonyl, 9-fluorenyImethoxycarbonyl, 2,2,2- trichloroethoxymethyl, trimethylsilyl, triethylsilyl, tripropylsilyl, dimethylethylsilyl, dimethyl(t-butyl)silyl, diethylmethylsilyl, dimethylphenylsilyl, diphenylmethylsilyl, acetyl, chloroacetyl, dichloroacetyl, trichloroacetyl and trifluoroacetyl.
46. The compound of claim 44 wherein Ri is a protected thiol group, and the protecting group is selected from triphenylmethyl (trityl, Trt), acetamidomethyl (Acm), benzamidomethyl, 1 -ethoxyethyl and benzoyl.
47. A process comprising the scheme
Figure imgf000079_0001
Ri is hydroxyl, protected hydroxyl, thiol, or protected thiol;
R2 is alkyl, alkenyl, alkynyl or aryl, where R2 may be optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms; and
PG is a protecting group.
48. A compound of the formula
Figure imgf000080_0001
Ri is hydroxyl, protected hydroxyl, thiol, protected thiol, alkyl, alkenyl, alkynyl, or aryl where Ri is optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms;
R2 is alkyl, alkenyl, alkynyl or aryl, where R2 may be optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms;
PG is a protecting group; and salts and esters thereof.
49. The compound of claim 48 wherein Ri is a protected hydroxyl group and the protecting group is selected from methoxymethyl, methoxyethyl, 1 -ethoxyethyl, benzyloxymethyl, (beta-trimethylsilyl- ethoxy)methyl, tetrahydropyranyl, 2,2,2-trichloro-ethoxycarbonyl, benzyloxycarbonyl, tet -butoxycarbonyl, 9-fluorenylmethoxycarbonyl, 2,2,2- trichloroethoxymethyl, trimethylsilyl, triethylsilyl, tripropylsilyl, dimethylethylsilyl, dimethyl(t-butyl)silyl, diethylmethylsilyl, dimethylphenylsilyl, diphenylmethylsilyl, acetyl, chloroacetyl, dichloroacetyl, trichloroacetyl and trifluoroacetyl.
50. The compound of claim 48 wherein Ri is a protected thiol group and the protecting group is selected from triphenylmethyl (trityl, Trt), acetamidomethyl (Acm), benzamidomethyl, 1 -ethoxyethyl and benzoyl.
51. A process of replacing a thioaryl group with a hydroxyl group according to the scheme
Figure imgf000081_0001
wherein PG is an amine protecting group, An and Ar2 are aryl groups, E is hydrogen or an organic group, and Hg represents a mercury-containing oxidizing agent.
52. The process of claim 51 wherein PG is benzoyl or tBOC.
53. The process of claim 51 wherein E is hydrogen or C-i-
C6alkyl.
54. The process of claim 51 wherein An and Ar2 are each phenyl.
55. The process of claim 51 wherein Hg is HgO or
Hg(CF3CO2)2.
56. A process of replacing a thioaryl group with a hydroxyl group according to the scheme
Figure imgf000081_0002
wherein Hg represents a mercuric reagent, and An and Ar2 are independently selected from alkyl, alkenyl, alkynyl, aryl or substituted aryl radical; and R10 is hydrogen, Ci-Cεalkyl, aryl or substituted aryl radical; wherein a substituted aryl radical is substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms.
57. The process of claim 56 wherein Hg is mercuric oxide or mercuric trifluoroacetate.
58. The process of claim 56 eerie ammonium nitrate (CAN) is utilized in the reaction.
59. The process of claim 56 wherein Rio is hydrogen.
60. The process of claim 56 wherein Rio is para- methoxyphenyl.
61. The process of claim 56 wherein An and Ar2 are each phenyl.
62. A process comprising esterifying a compound of the formula
Figure imgf000082_0001
wherein R6 is acetyl or dichloroacetyl; and R7 is triethylsilyl, dichloroacetyl or Troc; with an acid compound of a formula selected from
Figure imgf000083_0001
wherein
R8 is tBOC, PMP, Bz or H;
Rg is thiophenyl, acetoxy, methoxy, t-butoxycarbonyloxy, phenoxy, ethoxyethyl, or dichloroacetyl; and R-io is hydrogen.
63. The process of claim 62 wherein the acid compound has the formula
Figure imgf000083_0002
wherein An is phenyl and Rg is thiophenyl, acetoxy, methoxy, t-butoxycarbonyloxy, phenoxy, ethoxyethyl, or dichloroacetyl.
64. The process of claim 62 wherein the acid compound has the formula
Figure imgf000083_0003
wherein An is phenyl, R8 is tBOC, PMP or H, and Rg is acetoxy or a protected hydroxyl wherein the protecting group is ethoxyethyl.
65. The process of claim 62 wherein the acid compound has the formula
Figure imgf000084_0001
wherein An is phenyl, R8 is hydrogen or PMP, and Rg is thiophenyl, acetoxy, methoxy, t-butoxycarbonyloxy, phenoxy, ethoxyethyl, or dichloroacetyl.
66. A compound of the formula
Figure imgf000084_0002
wherein R and R are independently selected from hydrogen, triethylsilyl, acetyl and dichloroacetyl, with the proviso that Re and R may not be simultaneously hydrogen, R8 is tBOC, PMP, Bz or H, and Rg is thiophenyl, acetoxy, methoxy, t-butoxycarbonyloxy, ethoxyethyl or dichloroacetyl.
67. A compound of claim 66 wherein Re and R are each dichloroacetyl, R8 is tBOC and R9 is thiophenyl, acetoxy, methoxy, t-butoxycarbonyloxy, ethoxyethyl or dichloroacetyl.
68. A compound of claim 66 wherein R6 is acetyl, R7 is -TES, R8 is t-BOC, and Rg is thiophenyl, acetoxy, methoxy, t-butoxycarbonyloxy, ethoxyethyl or dichloroacetoxy.
69. A compound of claim 66 wherein R6 and R7 are each dichloroacetyl, R8 is tBOC, PMP or H, and Rg is acetoxy.
70. A compound of claim 66 wherein R5 is triethylsilyl, R6 is acetyl, R8 is tBOC, PMP, Bz or H, and R9 is acetoxy, ethoxyethyl or dichloroacetyl.
71. A process comprising the scheme
Figure imgf000085_0001
wherein R and R7 are independently selected from hydrogen, triethylsilyl, acetyl, Troc and dichloroacetyl, with the proviso that Re and R7 may not be simultaneously hydrogen, R8 is tBOC, PMP, Bz or H, and Rg is thiophenyl, acetoxy, methoxy, t-butoxycarbonyloxy, ethoxyethyl or dichloroacetyl.
72. The process of claim 71 wherein the compound of structure (I) is deprotected at the 2' position to form an intermediate of structure (la), and the intermediate is treated with zinc acetate dihydrate or urea to form the compound of formula (II), where the intermediate has the structure
Figure imgf000086_0001
73. The process of claim 71 wherein the compound of formula (I) is treated with protic acid and tertiary amine in an organic solvent to form an intermediate of formula (lb), and the intermediate is deprotected at the 2' position to form the compound of formula (II), where the intermediate has the structure
Figure imgf000086_0002
74. A method of preparing TAXOTERE, comprising reacting a compound of structure (III) with t-BOC, followed by deprotection of at least one of the 2', 7 and 10 positions, where the compound of structure (III) is
Figure imgf000087_0001
wherein R and R are independently selected from hydrogen, triethylsilyl, acetyl, Troc and dichloroacetyl, with the proviso that R and R may not be simultaneously hydrogen, and Rg is thiophenyl, acetoxy, methoxy, t-butoxycarbonyloxy, or dichloroacetyl or ethoxyethyl.
75. The method of claim 74 wherein Re and R are each dichloroacetyl and Rg is acetoxy or ethoxyethyl.
76. The method of claim 75 wherein the compound of structure (III) is prepared by the reduction of a compound of structure (IV)
Figure imgf000087_0002
wherein Re and R are each dichloroacetyl, Rg is acetoxy or ethoxyethyl, and R11 is OCOO-t-Bu.
77. The method of claim 74 wherein R is acetyl or dichloroacetyl, R is TES or Troc, and Rg is acetoxy or ethoxyethyl.
78. The method of claim 74 wherein the compound of structure (III) is prepared by the reduction of a compound of structure (IV)
Figure imgf000088_0001
wherein R6 is Ac, R7 is TES, R9 is acetoxy, and Rn is PMP, OCOO-t-Bu or H.
79. A process comprising the scheme
Figure imgf000088_0002
An and Ar2 are independently selected from alkyl, alkenyl, alkynyl, aryl or substituted aryl radical; and
Rio is hydrogen, Cι-C6alkyl, aryl or substituted aryl radical; wherein a substituted aryl radical is substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms.
80. A process of coupling a beta lactam to a baccatin compound according to the following scheme
Figure imgf000089_0001
wherein
R3 and R4 are independently selected from hydrogen, hydroxyl, protected hydroxyl, thiol, protected thiol, alkyl, alkenyl, alkynyl, or aryl where Ri is optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms;
R is hydroxyl or a protected hydroxyl group; and the coupling is performed by addition of metal hydride, metal alkoxide or lewis acid to the reaction mixture.
81. The method of claim 80 wherein the coupling is performed by the addition of sodium hydride.
82. The method of claim 80 wherein the coupling is performed by the addition of sodium hexamethyldisilazide.
83. A process of coupling a beta lactam to a baccatin III compound according to the following scheme
Figure imgf000090_0001
wherein
R3 and R are independently selected from hydrogen, hydroxyl, protected hydroxyl, thiol, protected thiol, alkyl, alkenyl, alkynyl, or aryl where R3 and R4 are optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms;
R is hydroxyl or a protected hydroxyl group; and the coupling is performed by addition of metal hydride, metal alkoxide or lewis acid to the reaction mixture.
84. The method of claim 83 wherein the coupling is performed by the addition of sodium hydride.
85. The method of claim 83 wherein the coupling is performed by the addition of sodium hexamethyldisilazide.
86. A method for making a compound of formulas (III) or (IV):
Figure imgf000091_0001
Figure imgf000091_0002
comprising the step of reacting a compound of formula (I)
Figure imgf000091_0003
with a compound of formula (lla) or (Mb)
Figure imgf000091_0004
wherein
Ri, R2, R3 and R are independently selected from hydrogen, hydroxyl, protected hydroxyl, thiol, protected thiol, alkyl, alkenyl, alkynyl, or aryl where R3 and R4 are optionally substituted with one or more of halogen, hydroxyl, alkoxy, aryloxy, heteroaryloxy, amino, alkylamino, dialkylamino, mercapto, alkylthio, arylthio, heteroarylthio, cyano, carboxyl, alkoxycarbonyl where the alkoxy portion contains 1 to 15 carbons, aryloxycarbonyl where the aryloxy portion contains 6 to 20 carbon, or heteroarylcarbonyl where the heteroaryl portion contains 3 to 15 carbon atoms;
R7 = -OCOCHCI2 or triethylsilyl; and
Rι2 is an amine protecting group.
87. The method of claim 86 wherein the compound of formula (I) is reacted with the compound of formula (lla).
88. The method of claim 87 wherein R-ι2 is tBOC.
89. The method of claim 88 wherein R7 is -OCOCHCI2.
90. The method of claim 89 wherein Ri is hydrogen and R2 is thiophenyl.
91. The method of claim 89 wherein Ri is OAc and R2 is thiophenyl
92. The method of claim 88 wherein is R7 is triethylsilyl.
93. The method of claim 92 wherein Ri is hydrogen and R2 is thiophenyl.
94. The method of claim 92 wherein Ri is OAc and R2 is thiophenyl
95. The method of claim 87 wherein Rι2 is benzoyl.
96. The method of claim 95 wherein R7 is -OCOCHCI2.
97. The method of claim 96 wherein Ri is hydrogen and R2 is thiophenyl.
98. The method of claim 96 wherein Ri is OAc and R2 is thiophenyl
99. The method of claim 95 wherein is R7 is triethylsilyl.
100. The method of claim 99 wherein Ri is hydrogen and R2 is thiophenyl.
101. The method of claim 99 wherein R-i is OAc and R2 is thiophenyl
102. The method of claim 86 wherein the compound of formula (I) is reacted with the compound of formula (lib).
103. The method of claim 102 wherein R 2 is tBOC.
104. The method of claim 103 wherein R7 is -OCOCHCI2.
105. The method of claim 104 wherein R3 is -OAc and R4 is thiophenyl.
106. The method of claim 104 wherein R3 is -OEE and R4 is thiophenyl.
107. The method of claim 103 wherein is R7 is triethylsilyl.
108. The method of claim 107 wherein R3 is -OAc and R4 is thiophenyl.
109. The method of claim 107 wherein R3 is -OEE and R4 is thiophenyl.
110. The method of claim 102 wherein Rι2 is benzoyl.
111. The method of claim 110 wherein R7 is -OCOCHCI2.
112. The method of claim 111 wherein R3 is -OAc and R4 is thiophenyl.
113. The method of claim 111 wherein R3 is -OEE and R4 is thiophenyl.
114. The method of claim 110 wherein is R7 is triethylsilyl.
115. The method of claim 114 wherein R3 is -OAc and R4 is thiophenyl.
116. The method of claim 114 wherein R3 is -OEE and R4 is thiophenyl.
117. The method of claim 86 wherein the compound of formula (l) is obtained from 9-dihydro-13 acetylbaccatin 111 (9DHB) via baccatin III intermediate.
118. The method of claim 86 wherein the compound of formula (lla) or (lib) is prepared from one or more reactants selected from para- methoxyaniline, benzaldehyde, thiophenoxyacetyl chloride, acetoxyacetyl chloride, ammonia and syn-benzaldehyde oxime.
119. The method of claim 86 wherein the compound of formula (lla) or (lib) comprises a thiophenyl group, and the thiophenyl group is hydrolyzed by a mercuric reagent.
120. The method of claim 119 wherein the mercuric reagent is mercuric oxide or mercuric trifluoroacetate.
121. The method of claim 86 wherein the compound of formula (III) or (IV) comprises a dichloroacetyl group, and the dichloroacetyl group is hydrolyzed by zinc acetate dihydrate or urea.
122. The method of claim 86 wherein the compound of formula (III) or (IV) comprises an acetate group, and the acetate group is removed by mild base and hydrogen peroxide.
123. The method of claim 122 wherein the mild base is sodium carbonate or sodium hydrogen carbonate.
124. The method of claim 86 wherein a paramethoxy phenyl or oxime protected t-BOC group is cleaved by reduction in an organic solvent to produce a primary amine at the 3' position.
125. The method of claim 86 further comprising the step of converting the compound of formula (III) or (IV) to paclitaxel.
126. The method of claim 86 further comprising the step of converting the compound of formula (III) or (IV) to taxotere.
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