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WO2008032104A1 - Synthèse en un creuset de dérivés de taxane et leur conversion en paclitaxel et docétaxel - Google Patents

Synthèse en un creuset de dérivés de taxane et leur conversion en paclitaxel et docétaxel Download PDF

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Publication number
WO2008032104A1
WO2008032104A1 PCT/GB2007/003524 GB2007003524W WO2008032104A1 WO 2008032104 A1 WO2008032104 A1 WO 2008032104A1 GB 2007003524 W GB2007003524 W GB 2007003524W WO 2008032104 A1 WO2008032104 A1 WO 2008032104A1
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Prior art keywords
taxane
protecting
hydroxy
protected
group
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PCT/GB2007/003524
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English (en)
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Ragina Naidu
Ross Thomson Walker
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Chatham Biotec Ltd.
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Publication of WO2008032104A1 publication Critical patent/WO2008032104A1/fr

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    • 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents

Definitions

  • the present invention relates to the semi-synthesis of taxane derivatives useful in the preparation of paclitaxel and docetaxel, in particular, the semi-synthesis of protected taxane derivatives in a one pot reaction
  • Taxol paclitaxel (1 , Taxol)
  • 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 is similar in structure to paclitaxel, having t-butoxycarbonyl instead of benzoyl on the amino group at the 3' position, and a hydroxy group instead of the acetoxy group at the C-10 position.
  • Taxanes are structurally complicated molecules, and the development of commercially viable synthetic methods to make taxanes has been a challenge.
  • a number of semi-synthetic pathways have been developed, which typically begin with the isolation and purification of a naturally occurring material followed by its conversion to a taxane of interest.
  • paclitaxel and taxotere may be prepared semi-synthetically from 10-deacetylbaccatin III or baccatin III as set forth in U.S. Patent No. 4,924,011 to Denis et al. and U.S. Patent No. 4,924,012 to Colin et al.
  • 10-deacetylbaccatin III 10-DAB, 3
  • baccatin III BACC III, 4
  • BACC III baccatin III
  • U.S. Patent Nos. 5,202,448 and 5,256,801 to Carver et al., U.S. Patent No. 5,449,790 to Zheng et al. and U.S. Patent No. 6,281 ,368 to McChesney et al. disclose processes for converting certain taxanes (namely, paclitaxel, cephalomannine, 10-deacetyl taxol and certain 10-deacetyl taxol derivatives) present in partially purified taxane mixtures into 10-deacetylbaccatin III and baccatin III, which may subsequently be utilized in the foregoing semisynthetic pathways.
  • taxanes namely, paclitaxel, cephalomannine, 10-deacetyl taxol and certain 10-deacetyl taxol derivatives
  • the present invention relates to the semi-synthesis of taxane intermediates useful in the preparation of paclitaxel and docetaxel, in particular, the semi-synthesis of protected taxane intermediates in a one pot reaction with yield of over 95%, as set forth below.
  • the present invention provides a process for protecting a taxane of Formula (I):
  • Z is -OH, d and G 2 are the same or different and independently a hydroxy protecting group
  • the process comprising: protecting the free hydroxy groups at the C-10 position and/or the C-7 position of the taxane, and attaching a side chain to the free hydroxy group at the C-13 position of the taxane to provide a C-13 protected taxane intermediate, wherein the steps of protecting and attaching comprises, in a one-pot reaction with over 95% yield, combining the taxane with a base, a suitable hydroxy protecting agent and a precursor to the side chain, and wherein the precursor to the side chain is a beta-lactam, oxazolidine or oxazoline.
  • the present invention provides a process for protecting a taxane of Formula (I), which is part of a mixture of taxanes comprising, in addition to the taxane of Formula (I), paclitaxel, 9-dihydro-13-acetylbaccatin III, cephalomannine, 10-deacetyl taxol, 7-xylosyl taxol and 10-deacetyl-7-xylosyl taxol.
  • the present invention provides a process for preparing paclitaxel or docetaxel, comprising: protecting the hydroxy group at the C-10 and/or C-7 position of a compound of formula (V): wherein, Z is -OH; attaching a side chain to the free hydroxyl group at C-13 position to provide a C-13 protected taxane intermediate; and converting the C-13 protected taxane intermediate to paclitaxel or docetaxel, wherein the steps of protecting and attaching comprise, combining in a one pot reaction with over 95% yield, the compound of Formula (V) with a base, a suitable hydroxy protecting agent and a precursor to the side chain, and wherein the precursor to the side chain is a beta-lactam, oxazolidine or oxazoline.
  • the present invention provides a process for preparing paclitaxel or docetaxel from an initial mixture of taxanes comprising 10-deacetylbaccatin III and at least one additional taxane selected from paclitaxel, 9-dihydro-13-acetylbaccatin III, baccatin III, cephalomannine, 10-deacetyl taxol, 7- xylosyl taxol and 10-deacetyl-7-xylosyl taxol, the process comprising: protecting the hydroxy group at the C-7 position of each taxane in the initial mixture having a hydroxy group at the C-7 position to yield a first intermediate mixture of C-7 protected taxanes; protecting the C-10 position of the taxane; attaching a side chain to the C-13 position of each taxane having a free hydroxy group at the C-13 position in the first intermediate mixture to provide a mixture of C-13 protected taxane intermediates; and converting the C-13 protected taxane intermediates to paclitaxe
  • Figure 1 illustrates a chemical route for the preparation of a C-13 beta-lactam protected taxane intermediate, and the conversion of such intermediate to paclitaxel and docetaxel according to the present invention.
  • Figure 2 illustrates several chemical routes for the preparation of beta-lactam side chains for use in the semi-synthetic processes of the present invention.
  • Figure 3 illustrates an alternative chemical route for the preparation of a beta-lactam side chain for use in the semi-synthetic processes of the present invention.
  • the present invention relates to the semi- synthesis of taxane intermediates useful in the preparation of paclitaxel and docetaxel, in particular, the semi-synthesis of protected taxane intermediates in a one pot reaction with over 95% yield.
  • Silica matrix is a solid media containing a silicate which is used as an adsorbent or column material in chromatographic separations, including (but not limited to) ordinary silica, Florisil, porous silica gels or any physical formulation of a silicate for use in chromatographic procedures.
  • Tuxane-containing material refers to selected parts of a plant, plant tissues, cell cultures, microorganisms or extracts with extractable taxanes, including paclitaxel, 10-deacetylbaccatin III (10-DAB) 1 baccatin III (BACC III), 9- dihydro-13-acetylbaccatin III (9-DHB), cephalomannine, 10-deacetyl taxol (10- DAT), 7-xylosyl taxol and 10-deacetyl-7-xylosyl taxol.
  • 10-DAB 10-deacetylbaccatin III
  • BACC III baccatin III
  • 9-DHB 9- dihydro-13-acetylbaccatin III
  • cephalomannine 10-deacetyl taxol (10- DAT), 7-xylosyl taxol and 10-deacetyl-7-xylosyl taxol.
  • Caste taxane extract refers to a composition obtained from a taxane-containing material by treating the taxane-containing material with at least one solvent.
  • Partially purified taxane extract refers to a paclitaxel enriched composition obtained from the chromatographic separation and/or recrystallization of a crude or partially purified taxane extract.
  • Wild stream fractions refers to fractions collected following the chromatographic separation and collection of paclitaxel enriched fractions from a crude or partially purified taxane extract by, for example, the process of U.S. Patent No. 6,136,989.
  • Wash mother liquors refers to mother liquors collected following the recrystallization of a crude or partially purified taxane extract by, for example, the process of U.S. Patent No. 6,136,989.
  • Hydro xy-protecting group refers to any derivative of a hydroxy group known in the art which can be used to mask the hydroxy group during a chemical transformation and later removed under conditions resulting in the hydroxy group being recovered without other undesired effects on the remainder of the molecule. Many esters, acetals, ketals and silyl ethers are suitable protecting groups.
  • hydroxy-protecting groups include, without limitation, formyl, acetyl (Ac), benzyl (PhCH 2 ), 1-ethoxyethyl (EE), methoxymethyl (MOM), (methoxyethoxy)methyl (MEM), (p-methoxyphenyl)methoxymethyl (MPM), tert- butyldimethylsilyl (TBS), tert-butyldiphenylsilyl (TBPS), tert-butoxycarbonyl (tBoc, t- Boc, tBOC, t-BOC), tetrahydropyranyl (THP), triphenylmethyl (Trityl, Tr), 2- methoxy-2-methylpropyl, benzyloxycarbonyl (Cbz), dichloroacetyl, thchloroacetyl (OCCCI 3 ), 2,2,2-trichloroethoxycarbonyl (Troc), benzyloxymethyl (BOM), benz
  • 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- trichloroethoxycarbonyloxy, benzyloxycarbonyloxy, tert-butoxycarbonyloxy, 1- cyclopropylethoxy
  • hydroxy protecting agent refers to a reagent that introduces a hydroxy protecting group to a free hydroxy functionality.
  • a hydroxy protecting agent comprises a hydroxy protecting group as those listed above and a leaving group, such as a halide or a triflate.
  • the hydroxy protecting group is an alkyl
  • the hydroxy protecting agent is referred herein as an alkylating agent.
  • the hydroxy protecting agent can be referred herein as an acylating agent or silylating agent, respectively. More exemplary hydroxy-protecting groups and hydroxy protecting agents are described in, e.g., C. B. Reese and E.
  • Thiol-protecting group refers to any derivative of a thiol group known in the art which can be used to mask the thiol group during a chemical transformation and later removed under conditions resulting in the thiol group being recovered without other undesired effects on the remainder of the molecule.
  • 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., Ci-C- ⁇ 0 alkylthio), -S-acyl (acylthio), thioacetal, -S-aralkyl (aralkylthio, e.g., aryl(Ci-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
  • Thiol-protecting groups and protected thiol 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.
  • Alkyl refers to an optionally substituted hydrocarbon structure, containing no saturation, wherein the carbons are arranged in a linear, branched or cyclic manner, including combinations thereof.
  • Lower alkyl refers to alkyl groups of
  • Cycloalkyl is a subset of alkyl and includes mono or bi-cyclic hydrocarbon groups of from 3 to 13 carbon atoms.
  • cycloalkyl groups include cyclopropyl, cyclobutyl, cyclopentyl, norbomyl, 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 ⁇ -propyl and isopropyl.
  • Alkenyl refers to an optionally substituted alkyl group having at least one site of unsaturation, i.e., at least one double bond.
  • Alkynyl refers to an optionally substituted alkyl group having at least one triple bond between two adjacent carbon atoms.
  • Alkoxy refers to a radical of the formula -O-alkyl. Examples include methoxy, ethoxy, propoxy, isopropoxy, cyclopropyloxy, cyclohexyloxy and the like. Lower-alkoxy refers to groups containing one to five carbons.
  • Alkoxycarbonyl refers to a radical of the formula -C(O)-alkoxy, wherein alkoxy is as defined herein.
  • Aryl refers to optionally substituted phenyl or naphthyl.
  • exemplary substituents for aryl include one or more of halogen, hydroxy, 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.
  • Aryloxy refers to a radical of the formula -O-aryl, wherein aryl is defined as above. Representative aryloxy includes phenoxy.
  • Aryloxycarbonyl refers to a radical of the formula -C(O)-aryloxy, wherein aryloxy is as defined herein.
  • Heteroaryl refers to an optionally substituted 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 1-3 heteroatoms selected from O, N or S; or a tricyclic 13- or 14-membered heteroaromatic ring system containing 1-3 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.
  • Heterocycle means a 5- to 7-membered monocyclic, or 7- to 10- membered bicyclic, heterocyclic ring which is either saturated, unsaturated or aromatic, and which contains from 1 to 4 heteroatoms independently selected from nitrogen, oxygen and sulfur, and wherein the nitrogen and sulfur heteroatoms may be optionally oxidized, and the nitrogen heteroatom may be optionally quaternized, including bicyclic rings in which any of the above heterocycles are fused to a benzene ring.
  • the heterocycle may be optionally substituted with 1-5 substituents.
  • the heterocycle may be attached via any heteroatom or carbon atom.
  • Heterocycles include heteroaryls as defined above.
  • heterocycles also include morpholinyl, pyrrolidinonyl, pyrrolidinyl, piperidinyl, piperazinyl, hydantoinyl, valerolactamyl, oxiranyl, oxetanyl, tetrahydrofuranyl, tetrahydropyranyl, tetrahydropyridinyl, tetrahydroprimidinyl, tetrahydrothiophenyl, tetrahydrothiopyranyl, tetrahydropyrimidinyl, tetrahydrothiophenyl, tetrahydrothiopyranyl, and the like.
  • Representative acyl groups include acetyl, benzoyl, propionyl, isobutyryl, t- butoxycarbonyl, and the like. Lower-acyl refers to groups containing one to five carbons.
  • leaving group refers to a chemical moiety that may be displaced during a substitution or elimination reaction.
  • exemplary leaving groups include halogen (e.g., bromide and chloride), triflate and tosyl.
  • Halogen refers to fluoro, chloro, bromo or iodo.
  • Haldrocarbonyl refers to alkyl, alkenyl, alkynyl or aryl.
  • one pot reaction also referred to herein as a "one pot synthesis” refers to a multi-step chemical reaction carried out in a reaction vessel.
  • a reaction intermediate is generated in an initial step of reaction, the intermediate is then reacted in situ with other component(s) present in or introduced to the same vessel.
  • the reaction intermediate generated is not isolated but serves directly as a reactant in a next step of reaction.
  • a free hydroxy group of a taxane is protected, the protected intermediate is not isolated and is used directly in a next step wherein a side chain is attached to a free hydroxy group of the taxane intermediate.
  • the present invention relates to a semi-synthesis process of taxane intermediates useful in the preparation of paclitaxel and docetaxel, in particular, the semi-synthesis of protected taxane intermediates.
  • one embodiment of the present invention provides a process comprising novel combined steps of protecting the C10 position of a taxane of Formula (I) and attaching a side chain to the free hydroxy group at C13 position in a one-pot reaction to provide a C13 protected taxane intermediate (III) in over 95% yield.
  • the process comprises combining, in one reaction vessel, a taxane of Formula (I) with a base, a hydroxy protecting agent and a precursor to the side chain, for example, a compound of Formula (II).
  • a taxane of Formula (I) with a base, a hydroxy protecting agent and a precursor to the side chain, for example, a compound of Formula (II).
  • a general reaction scheme is shown below:
  • R 1 is a hydroxy group, protected hydroxy group, thiol group or protected thiol group
  • R 2 is alkyl, alkenyl, alkynyl or aryl
  • R 3 is hydrogen, C- 1 -C-6 alkyl, aryl or acyl
  • Z is -OR 4 or OH ;
  • R 4 and R 5 are the same or different and independently a hydroxy protecting group
  • G 1 and G 2 are the same or different and independently a hydroxy protecting group.
  • the protection step comprises protecting the hydroxy group at C-10 position as a result
  • R 4 and R 5 of Formula (III) are the same or different hydroxy protecting groups.
  • the protection step comprises protecting the hydroxy group at C-7 position only, as a result, R 4 and R 5 of Formula (III) can be the same or different hydroxy protecting groups.
  • the precursor to the side chain can be an oxazolidine or oxazoline.
  • hydroxy groups at the C-7 and/or C-10 positions of a taxane of Formula (I) can be selectively protected using any of a variety of hydroxy protecting agents, such as acetal, ketal, silyl, and removable acyl protecting groups, in the presence of a base, wherein Formula (I) is:
  • Z is -OR 4 or OH
  • R 4 , G 1 and G 2 are the same or different and independently a hydroxy protecting group.
  • the C-7 and/or C-10 hydroxy group may be silylated using any of a variety of common silylating agents including, but not limited to, tri(hydrocarbonyl)silyl halides and tri(hydrocarbonyl)silyl triflates.
  • the hydrocarbonyl moieties of these compounds may be optionally substituted and preferably are substituted or unsubstituted alkyl or aryl.
  • the C-7 and/or C-10 hydroxy group can be selectively siiylated, for example, using silylating agents such as tribenzylsilyl chloride, trimethylsilyl chloride, triethylsilyl chloride, dimethylisopropylsilyl chloride, dimethylphenylsilyl chloride and the like.
  • silylating agents such as tribenzylsilyl chloride, trimethylsilyl chloride, triethylsilyl chloride, dimethylisopropylsilyl chloride, dimethylphenylsilyl chloride and the like.
  • selective acylation of the C-7 and/or C-10 hydroxy group can be achieved using any of a variety of common acylating agents, but not limited to substituted and unsubstituted carboxylic acid derivatives, e.g., carboxylic acid halides, anhydrides, dicarbonates, isocyanates and haloformates.
  • carboxylic acid halides e.g., carboxylic acid halides, anhydrides, dicarbonates, isocyanates and haloformates.
  • the C-7 and/or C-10 hydroxy group can be selectively acylated, for example, with di-tert-butyl dicarbonate (BOC2O), dibenzyl dicarbonate, diallyl dicarbonate, 2,2,2-trichloroethyl chloroformate, benzyl chloroformate, dichloroacetyl chloride, acetyl chloride or another common acylating agent.
  • BOC2O di-tert-butyl dicarbonate
  • dibenzyl dicarbonate dibenzyl dicarbonate
  • diallyl dicarbonate 2,2,2-trichloroethyl chloroformate
  • benzyl chloroformate 2,2,2-trichloroethyl chloroformate
  • dichloroacetyl chloride acetyl chloride or another common acylating agent.
  • Suitable base for the protecting step includes, for example, DMAP, pyridine, TEA, LiOH, Li-t-OBu, n-BuLi, LiH, LiHMDS, KHMDS, K-t-OBu, NaH, NaHMDS and a mixture of any two or more of the foregoing, such as a mixture of n-BuLi/Li-t-Obu.
  • Exemplary reaction conditions are as follows: a taxane of Formula (I), or a mixture of taxanes, is dissolved in an organic solvent, such as anhydrous DCM (dichloromethane) or THF (tetrahydrofuran) or DMF (dimethyl formamide) or DMSO (dimethyl sulfoxide) or acetonitrile or any of the above mixtures for example THF and DCM or DMF and DCM etc. under an argon atmosphere at temperature range of 25 to -78 0 C.
  • an organic solvent such as anhydrous DCM (dichloromethane) or THF (tetrahydrofuran) or DMF (dimethyl formamide) or DMSO (dimethyl sulfoxide) or acetonitrile or any of the above mixtures for example THF and DCM or DMF and DCM etc.
  • an organic solvent such as anhydrous DCM (dichloromethane) or THF (tetrahydrofuran) or DMF
  • DMAP dimethylaminopyridine
  • any of the lithium, sodium or potassium base such as Li-t-OBu, K-t-OBu, n-BuLi, a mixture of n-BuLi/K-t-OBu or LiOH
  • a hydroxy protecting agent such as an acylating agent (e.g., di-tert-butyl dicarbonate or 2,2,2-trichloroethyl chloroformate etc.), a silylating agent (e.g., triethyl silyl chloride) or any other hydroxy protecting agent containing a hydroxy-protecting group.
  • Low temperature refers to temperature between -78 to room temperature.
  • An ester linkage at the C-13 position of the above taxane may be formed in the same combined step by adding to the C-7 and C-10 protected taxane, a base and a precursor to the side chain.
  • Representative base includes DMAP, TEA, LiOH, Li-t-OBu, n-BuLi, LiH, LiHMDS, KHMDS, K-t-OBu, NaH, NaHMDS or a mixture of any two or more of the foregoing.
  • the combined step may further comprise combining the taxane with a metal alkoxide, wherein the metal is selected from the group consisting of Group I, Il and III metals and transition metals.
  • Representative precursors to the side chains are described in more detail below, and include beta-lactams of Formula (II):
  • R 1 is a hydroxy group, protected hydroxy group, thiol group or protected thiol group
  • R 2 is alkyl, alkenyl, alkynyl or aryl; and R 3 is hydrogen, CrC 6 alkyl, aryl or acyl.
  • An exemplary reaction condition for the C-13 attachment includes, dissolving a taxane resulting from the preceding protection step and having a free hydroxy group at the C-13 position, or a mixture of .taxanes, in an organic solvent under an argon temperature at low temperature, for example, -78 0 C to room temperature.
  • a base such as DMAP, TEA, LiOH, Li-t- OBu, n-BuLi, LiH, LiHMDS, KHMDS, K-t-OBu, NaH, NaHMDS or a mixture of any two or more of the foregoing, followed by addition of a solution of beta-lactam.
  • the mixture is left to react at low to room temperature until complete consumption of the starting material, as visualized by TLC.
  • a solution of an acid, such as AcOH, in an organic solvent is added to the mixture, and the mixture is partitioned between saturated aqueous sodium hydrogen carbonate and mixtures of DCM and ethyl acetate.
  • the combined organic extracts are dried and evaporated to give the crude C-13 beta-lactam protected taxane intermediate, which can be further purified by column chromatography or crystallized from a suitable solvent.
  • taxanes of Formula (I) may be utilized to convert taxanes of Formula (I) into protected taxane intermediates, which can then be used to further synthesize paclitaxel and docetaxel.
  • Representative taxanes of Formular (I) include 10-deacetylbaccatin III (3) and baccatin III (4).
  • other taxanes may also be present in the starting material without affecting the conversion of Formula (I) to Formula (III), as illustrated in Reaction Scheme 1.
  • taxanes present in a crude taxane extract or in a waste taxane solution may be present, in addition to a taxane of Formular (I).
  • Representative taxanes can be present in the disclosed processes include ⁇ -dihydro-IS-acetylbaccatin III, paclitaxel, cephalomannine, 10-deacetyl taxol, 7-xylosyl taxol and 10-deacetyl-7-xylosyl taxol.
  • the taxanes utilized in the processes of the present invention may be pure, purified or partially purified taxanes.
  • Such purified and partially purified taxanes may be obtained by any of a number of different methods well known in the art.
  • 10 deacetylbaccatin III can be obtained by the methods described in Gunawardana et al., J. Nat. Prod. 55:1686 (1992); U.S. Patent No. 5,530,020 to Gunawardana et al.; U.S. Patent Nos. 5,202,448 and 5,256,801 to Carver et al., U.S. Patent No. 5,449,790 to Zheng et al. and U.S. Patent No.
  • the mixture of taxane utilized in the processes of the present invention may be a plurality of taxanes present in a crude taxane extract or in a waste taxane solution.
  • the disclosed processes may be utilized for high yield and large scale conversion of taxanes present in a waste taxane solution into beta-lactam protected taxane intermediates, which can be used to further synthesize paclitaxel and docetaxel.
  • Such waste taxane solutions may comprise (1) pooled waste stream fractions collected following the chromatographic separation and collection of paclitaxel enriched fractions from a crude or partially purified taxane extract, and/or (2) pooled waste mother liquors collected following the recrystallization of a crude or partially purified taxane extract.
  • Representative waste taxane solutions may be obtained by a number of different methods, such as, for example, the methods disclosed in U.S. Patent No. 6,136,989 to Foo et al., and other references cited therein, which patent is incorporated herein by reference in its entirety, and U.S. Patent Application No. 10/831 ,648, which application is assigned to the assignee of the present invention and is incorporated herein by reference in its entirety.
  • a representative method of obtaining a waste taxane solution which comprises pooled waste stream fractions, comprises the following extraction and column chromatography steps.
  • a suitable taxane-containing material is any tissue that contains a high taxane content.
  • suitable taxane-containing material include tissues from various species of Yew plants comprising the genus Taxus, most preferably the roots and needles of ornamental Yew plants such as T. canadensis, T. x media spp Hicksii, T. x dark green spreader and Hill., T. chinensis, T. wallichiana, T. cuspidata, T. globosa, T. sumatrana, T. marei and T. floridana, and the bark of T. brevifolia or T. yunnanensis.
  • Other suitable material includes cultures of plant tissues obtained from a Taxus species.
  • the taxane-containing material is either pulverized chipped or otherwise ground into small pieces so as to increase efficiency of a solvent extraction.
  • the taxane- containing material may also optionally be dried. Taxane-containing cell culture, cells, microorganisms and fermentation broths will typically be concentrated prior to solvent extraction. Cells and microorganisms can be processed as whole cells or cell paste or pulver.
  • the taxane-containing material may be initially extracted by contacting the material with an organic solvent, usually for a prolonged period of at least 8 hours and typically for about 3 days with or without physical agitation to promote formation of a crude organic extract containing a plurality of taxanes.
  • the extraction may employ any of the solvent systems that are known to be used for the extraction of paclitaxel, including but not limited to, acetone, methanol, ethanol, ethyl acetate, methylene chloride, chloroform, mixtures thereof, and mixtures containing an aqueous component of up to 60%. These solvents are typically added in an amount of about 4-20 liter per kg of the taxane-containing material to prepare the crude organic extract.
  • the organic solvent is a polar organic solvent, typically an alcohol.
  • methanol is preferred because of its low cost, ease of removal and efficiency of taxane extraction.
  • about 6-15 liters of methanol is added for every kg of taxane-containing material to be extracted.
  • the extraction is accelerated by agitating the taxane-containing material, for example, by stirring or percolating the methanol with the taxane- containing material for about 1-5 days at a temperature between room temperature and about 60°C, most typically at about 40°C.
  • methanol extraction for three days as described above recovers at least 90% of the available paclitaxel from the taxane-containing material, in addition to a plurality of other taxanes, to form a crude methanol extract containing about 0.1-0.5% paclitaxel and having an overall solid content of about 0.5-5% (w/v).
  • the large volume of methanol extract thus obtained is optionally concentrated, typically about 10-30 fold by evaporation to obtain a methanol extract concentrate having a solid content of about 100-400 g/L.
  • the crude organic extract may be subsequently enriched for taxanes by performing 1-3 liquid-liquid extractions by mixing the organic extract with a non- miscible, organic solvent to form a two phase system wherein one phase contains the plurality of taxanes.
  • the two phase system includes a polar phase.
  • the taxane-containing phase is selected and concentrated by evaporation to form a concentrated extract having a solid content of about 100-400 g/L and a paclitaxel purity of about 1-4%.
  • water is included to help remove preferentially water soluble materials and the less polar solvent is selected to remove undesirable compounds such as waxes, lipids, pigments, and sterols that are found in different amounts depending on the taxane-containing material used.
  • Typical solvents for liquid-liquid partitioning include hexane and methylene chloride. Methylene chloride has generally been found to be suitable for liquid-liquid extraction of taxane-containing material especially when the solvent used for the crude organic extract is an alcohol.
  • the concentrated extract obtained is optionally evaporated and the residue is re-dissolved in a solvent for loading onto a silica chromatography matrix.
  • liquid-liquid extraction may be omitted altogether when a plant extract containing high taxane levels is obtained by other methods such as for example, by intervening precipitation, crystallization or chromatography steps.
  • PCT Publication Nos. WO 98/07712 by Zamir et al which uses a precipitation step immediately after obtaining an initial organic extract to obtain a paclitaxel fraction that may be about 1 % or higher.
  • the concentrated extract may be further purified by normal phase silica chromatography.
  • silica chromatography generally refers to the process of contacting a sample dissolved in a feed solvent with a silica matrix then eluting the silica matrix with an eluting solvent to obtain a fraction enriched with a desired component.
  • the dimensions of the first silica column are selected according to the quantity and purity of the solids to be separated.
  • a pilot scale process about 250 grams of solids are dissolved in about 0.75 liters of feed solvent which is then chromatographed over a Silica column of about 1.5- inches x 10-feet.
  • about 40-50 kg of solids are dissolved in about 100-200 liters of feed solvent, and chromatographed over a Silica column of about 18-inches x 10-feet.
  • the optimal eluting solvent for the Silica column should be a hexane/acetone mixture at a ratio of about 3:1 or a DCM/ethyl acetate mixture at a ratio of about 7:3.
  • the "heart cut" fractions containing at least 2% paclitaxel are pooled and further purified, for example, according to the process set forth in U.S. Patent No. 6,136,989.
  • the remaining waste stream fractions which contain a plurality of taxanes, including, paclitaxel, 10-deacetylbaccatin III (10-DAB), baccatin III (BACC III), 9-dihydro-13-acetylbaccatin III (9-DHB), cephalomannine, 10-deacetyl taxol (10- DAT), 7-xylosy! taxol and 10-deacetyl-7-xylosyl taxol are pooled into a waste taxane solution for further processing according to the present invention.
  • 10-deacetylbaccatin III 10-DAB
  • BACC III baccatin III
  • 9-DHB 9-dihydro-13-acetylbaccatin III
  • cephalomannine 10-deacetyl taxol (10- DAT), 7-xylosy! taxol and 10-deacetyl-7-xylosyl taxol are pooled into a waste taxane solution for further processing according to the present
  • the paclitaxel enriched "heart cut" fractions obtained from the foregoing chromatography step may be further purified through one or more additional chromatographic or recrystallization steps. Any waste stream fractions or waste mother liquors collected during such additional purification steps may also be pooled and added to the waste taxane solution for further processing according to the present invention.
  • the precursors to the side chains utilized in the semi-synthetic processes of the present invention can be beta-lactams, oxazolidines or oxazolines. As illustrated by the following examples and the attached figures, such precursors may be reacted with a taxane having a free hydroxyl group at the C-13 position according to processes of the present invention in order to attach a side chain to the C-13 position of the taxane.
  • Representative beta-lactams are compounds of Formula (II):
  • R 1 is a hydroxy group, protected hydroxy group, thiol group or protected thiol group
  • R 2 is alkyl, alkenyl, alkynyl or aryl
  • R 3 is hydrogen, C 1 -C 6 alkyl, aryl or acyl; As described in U.S. Patent Application Nos. 10/683,865 and
  • beta-lactams may be prepared according to Reaction Scheme 2: REACTION SCHEME 2
  • beta-lactams may be prepared by (1) converting cinnamoyl halide to a cinnamoyl halide aziridine intermediate having the structure:
  • the protected taxane intermediates prepared according to the foregoing semi-synthetic processes may be utilized to further synthesize paclitaxel and docetaxel.
  • the present invention provides an overall process for preparing paclitaxel and/or docetaxel, comprising:
  • Z is -OH and P is a hydroxy protecting group
  • P is a hydroxy protecting group
  • the steps of protecting and attaching comprise combining the compound of Formula (V) with a base, a suitable hydroxy protecting agent and a precursor to the side chain in a one pot reaction with over 95% yield, and wherein the precursor to the side chain is beta-lactams, oxazolidines or oxazolines.
  • Z can be any suitable hydroxy protecting group as described herein, in one embodiment, Z is -OAc, the compound of Formula (V) is therefore a C-7 protected baccatin III. When Z is a free -OH, the compound of Formula (V) is C-7 protected 10 deacetylbaccatin III.
  • Suitable base for the protecting and attaching steps are as described above.
  • the present invention provides an overall process for preparing paclitaxel and/or docetaxel from an initial mixture of taxanes, wherein the initial mixture comprises 10-deacetylbaccatin III and at least one additional taxane selected from paclitaxel, baccatin III, cephalomannine, 9-dihydro- 13-acetylbaccatin III, 10-deacetyl taxol, 7-xylosyl taxol and 10-deacetyl-7-xylosyl taxol, the process comprising: (1) protecting the hydroxy group at the C-7 position of each taxane in the initial mixture having a hydroxy group at the C-7 position to provide a first intermediate mixture of C-7 protected taxanes;
  • step of protecting the C-10 hydroxy group and attaching a side chain to the free hydroxy at the C-13 position comprises, combining in one pot with over 95% yield, the initial mixture with a base, a suitable hydroxy protecting agent and a precursor to the side chain, and wherein the precursor to the side chain is beta-lactams, oxazolidines or oxazolines.
  • the step of protecting the hydroxy group at the C-7 position of each taxane in the initial mixture further comprises protecting a hydroxy group at the C-10 position of each taxane in the initial mixture having a hydroxy group at the C-10 position.
  • the initial mixture comprises: (1) 10- deacetylbaccatin III and at least two additional taxanes selected from paclitaxel, 9- dihydro-13-acetylbaccatin III, baccatin III, cephalomannine, 10-deacetyl taxol, 7- xylosyl taxol and 10-deacetyl-7-xylosyl taxol; (2) 10-deacetylbaccatin III and at least three additional taxanes selected from paclitaxel, 9-dihydro-13-acetylbaccatin III, , baccatin III, cephalomannine, 10-deacetyl taxol, 7-xylosyl taxol and 10- deacetyl-7-xylosyl taxol; or (3) 10-deacetylbaccatin III, 9-dihydro-13-acetylbaccatin III, paclitaxel, baccatin III, cephalomannine, 10-deacetyl
  • the initial mixture of taxanes is a waste taxane solution comprising one or more of the following: (1 ) pooled waste stream fractions collected during a chromatographic separation of a crude or partially purified taxane extract; and (2) pooled waste mother liquors collected during a recrystallization of a crude or partially purified taxane extract.
  • the waste taxane solution comprises: (1) pooled waste stream fractions collected during a chromatographic separation of a crude taxane extract; and (2) pooled waste stream fractions collected during chromatographic separations of both crude and partially purified taxane extracts and pooled waste mother liquors collected during recrystallizations of both crude and partially purified taxane extracts.
  • the first solvent is tetrahydrofuran. It is preferred to cool the first solution to a temperature of at least -4O 0 C. Where the starting compound is either 10 deacetylbaccatin II! or C-7 protected 10 deacetylbaccatin or baccatin III, it is preferred to add at least two equivalents of the base.
  • the method described above can be expanded by adding the step of warming the second solution to at least O 0 C over a selected period of time, such as one hour. Further, the second solution may then be quenched with an agent effective to eliminate any excess of base and any excess of protecting agent in the solution to form a third solution. The method then includes concentrating the third solution to form a crude residue and purifying.
  • the purification methodology may be accompanied by column chromatography or crystallization.
  • the resulting C-13 protected taxane intermediates may be converted to paclitaxel and docetaxel by a number of different methods, such as, for example, the methods disclosed in U.S. Patent Application Nos. 10/683,865 and 10/790,622, which applications are assigned to the assignee of the present invention and are incorporated herein by reference in their entireties, and U.S. Patent Nos. 6,365,750 and 6,307,071 , and the references cited therein, which patents and references are incorporated herein by reference in their entireties.
  • the solution was slowly warmed to near O 0 C and kept at that temperature for an additional 1 to 3 hrs, or until complete consumption of the starting material, as evidenced by TLC, before addition of a solution of an acid in an organic solvent, such as 10% AcOH in THF.
  • an organic solvent such as 10% AcOH in THF.
  • the mixture was then partitioned between saturated aqueous sodium hydrogen carbonate and ethyl acetate or mixtures of dichloromethane and ethyl acetate. Evaporation of the organic layer yielded a crude C-13 beta-lactam protected taxane intermediate, which could be further purified by either column chromatography or crystallization to yield a pure C-13 beta-lactam protected taxane intermediate or used directly for the next step.
  • the C-13 beta-lactam protected taxane intermediate was hydrolyzed using formic acid to remove the C-7 and/or C-10 BOC protecting group; HF/pyridine or Zn/HCI for TROC etc. and then with a mixture of NaHCO 3 ZNa 2 CO 3 ZH 2 O 2 to deprotect the C-2' andZor C-10 acetate groups to yield docetaxel, as described in U.S. Patent Application No. Application No. 10Z790.622, which application is assigned to the assignee of the present invention and is incorporated herein by reference in its entirety.

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Abstract

L'invention concerne un procédé pour la semi-synthèse d'intermédiaires du taxane, utiles dans la préparation de paclitaxel et de docétaxel, en particulier, la semi-synthèse d'un intermédiaire de taxane protégé dans une réaction en un creuset, consistant à protéger le C-10 et à attacher une chaîne latérale en position C-13 et, par la suite, à déprotéger le groupe afin de former du paclitaxel ou du docétaxel. L'invention concerne également les intermédiaires utilisés dans cette semi-synthèse.
PCT/GB2007/003524 2006-09-15 2007-09-17 Synthèse en un creuset de dérivés de taxane et leur conversion en paclitaxel et docétaxel WO2008032104A1 (fr)

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009137084A3 (fr) * 2008-05-07 2010-02-11 Ivax Research, Llc Processus de préparation des taxanes et de leurs intermédiaires
WO2010057378A1 (fr) * 2008-11-19 2010-05-27 上海百灵医药科技有限公司 Procédé pour la préparation de docétaxel, ses intermédiaires et leurs procédés de préparation
WO2013057260A1 (fr) 2011-10-19 2013-04-25 BARTON, Matthew Thomas Cabazitaxel, composés apparentés et procédés de synthèse

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20050288520A1 (en) * 2004-06-25 2005-12-29 Phytogen Life Sciences Inc. One pot synthesis of taxane derivatives and their conversion to paclitaxel and docetaxel
FR2882362A1 (fr) * 2005-02-23 2006-08-25 Seripharm Procede de preparation du paclitaxel

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20050288520A1 (en) * 2004-06-25 2005-12-29 Phytogen Life Sciences Inc. One pot synthesis of taxane derivatives and their conversion to paclitaxel and docetaxel
FR2882362A1 (fr) * 2005-02-23 2006-08-25 Seripharm Procede de preparation du paclitaxel

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009137084A3 (fr) * 2008-05-07 2010-02-11 Ivax Research, Llc Processus de préparation des taxanes et de leurs intermédiaires
WO2010057378A1 (fr) * 2008-11-19 2010-05-27 上海百灵医药科技有限公司 Procédé pour la préparation de docétaxel, ses intermédiaires et leurs procédés de préparation
JP2011510027A (ja) * 2008-11-19 2011-03-31 上海百霊医薬科技有限公司 ドセタキセル（Ｄｏｃｅｔａｘｅｌ）の合成プロセス、その中間体及びその合成法
WO2013057260A1 (fr) 2011-10-19 2013-04-25 BARTON, Matthew Thomas Cabazitaxel, composés apparentés et procédés de synthèse

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