Claims
- 1. A method for preparing taxane derivatives comprising:
- (a) obtaining a compound of formula (I): ##STR18## by hydrogenolyzing a compound of the formula (II): ##STR19## wherein in formulae (I) and (II): Ar represents an aryl radical;
- R represents a hydrogen atom, an alkyl radical containing 1 to 4 carbon atoms, or a phenyl radical, wherein the alkyl radical may be substituted by a phenyl radical; and
- Ph represents a phenyl radical unsubstituted or substituted by at least one atom or radical selected from halogen atoms, alkoxy radicals containing 1 to 4 carbon atoms, alkylthio radicals containing 1 to 4 carbon atoms, amino radicals, alkylamino radicals containing 1 to 4 carbon atoms, and dialkylamino radicals in which each alkyl portion contains 1 to 4 carbon atoms;
- (b) converting the formula (I) compound to a compound of the formula (VIII): ##STR20## wherein: Ar is defined as above;
- R.sub.3 represents a phenyl radical unsubstituted or substituted by at least one atom or radical, which are identical or different, selected from halogen atoms, alkyl, hydroxyl, alkoxy, alkanoyl, alkanoyloxy, nitro, amino, alkylamino, dialkylamino, carbamoyl, and trifluoromethyl radicals, the alkyl radicals and the alkyl portions of the other radicals containing 1 to 4 carbon atoms, or R.sub.3 represents a radical R.sub.4 --O-- in which R.sub.4 represents:
- a straight or branched alkyl radical containing 1 to 8 carbon atoms, an alkenyl radical containing 3 to 6 carbon atoms, a cycloalkyl radical containing 3 to 6 carbon atoms, a cycloalkenyl radical containing 4 to 6 carbon atoms, these radicals unsubstituted or substituted by at least one substituent selected from halogen atoms, hydroxyl radicals, alkyloxy radicals containing 1 to 4 carbon atoms, dialkylamino radicals in which each alkyl portion contains 1 to 4 carbon atoms, piperidino radicals, morpholino radicals, 1-piperazinyl radicals (unsubstituted or substituted by an alkyl radical containing 1 to 4 carbon atoms or by a phenylalkyl radical whose alkyl portion contains 1 to 4 carbon atoms), cycloalkyl radicals containing 3 to 6 carbon atoms, alkenyl radicals containing 4 to 6 carbon atoms, phenyl radicals, cyano radicals, carboxy radicals, and alkyloxycarbonyl radicals whose alkyl portion contains 1 to 4 carbon atoms;
- a phenyl radical which is unsubstituted or substituted by at least one atom or radical selected from halogen atoms, alkyl radicals containing 1 to 4 carbon atoms, and alkyloxy radicals containing 1 to 4 carbon atoms; or
- a saturated or unsaturated nitrogen-containing heterocyclic radical containing 4 to 6 members and unsubstituted or substituted by at least one alkyl radical containing 1 to 4 carbon atoms; and
- G.sub.3 represents a group which protects the hydroxyl functional group;
- (c) reacting the formula (VIII) compound with a taxane derivative of the formula (IX): ##STR21## to obtain a product of formula X: ##STR22## wherein in formulae (IX) and (X), Ar, R.sub.3, G.sub.3 are defined as above, G.sub.1 represents a group which protects the hydroxyl functional group, and G.sub.2 represents an acetyl radical or a group which protects the hydroxyl functional group; and
- (d) replacing the groups G.sub.1 and G.sub.3 by hydrogen atoms, and replacing G.sub.2 by a hydrogen atom when G.sub.2 represents an hydroxyl-protecting group, to obtain a taxane compound of the formula (VIl): ##STR23## in which Ar and R.sub.3 are defined as above and R.sub.2 represents a hydrogen atom or an acetyl radical.
- 2. The method of claim 1, wherein Ar represents a phenyl or an .alpha.- or .beta.-naphthyl radical which is unsubstituted or substituted by at least one atom or radical selected from halogen atoms, alkyl, aryl, aralkyl, alkoxy, alkylthio, aryloxy, arylthio, hydroxy, hydroxyalkyl, mercapto, formyl, acylamino, aroylamino, alkoxycarbonylamino, amino, alkylamino, dialkylamino, carboxy, alkoxycarbonyl, carbamoyl, dialkylcarbamoyl, cyano, nitro, and trifluoromethyl radicals, wherein the alkyl radicals and the alkyl portions of the other radicals contain 1 to 4 carbon atoms and the aryl radicals are phenyl or .alpha.- or .beta.-naphthyl radicals.
- 3. A method for preparing taxane derivatives comprising:
- (a) converting a formula (I) compound: ##STR24## to a compound of the formula (VIII): ##STR25## wherein: Ar represents an aryl radical;
- R represents a hydrogen atom, an alkyl radical containing 1 to 4 carbon atoms, or a phenyl radical, wherein the alkyl radical may be substituted by a phenyl radical; and
- R.sub.3 represents a phenyl radical unsubstituted or substituted by at least one atom or radical, which are identical or different, selected from halogen atoms, alkyl, hydroxyl, alkoxy, alkanoyl, alkanoyloxy, nitro, amino, alkylamino, dialkylamino, carbamoyl, and trifluoromethyl radicals, the alkyl radicals and the alkyl portions of the other radicals containing 1 to 4 carbon atoms, or R.sub.3 represents a radical R.sub.4 --O-- in which R.sub.4 represents:
- a straight or branched alkyl radical containing 1 to 8 carbon atoms, an alkenyl radical containing 3 to 6 carbon atoms, a cycloalkyl radical containing 3 to 6 carbon atoms, a cycloalkenyl radical containing 4 to 6 carbon atoms, these radicals unsubstituted or substituted by at least one substituent selected from halogen atoms, hydroxyl radicals, alkyloxy radicals containing 1 to 4 carbon atoms, dialkylamino radicals in which each alkyl portion contains 1 to 4 carbon atoms, piperidino radicals, morpholino radicals, 1-piperazinyl radicals (unsubstituted or substituted by an alkyl radical containing 1 to 4 carbon atoms or by a phenylalkyl radical whose alkyl portion contains 1 to 4 carbon atoms), cycloalkyl radicals containing 3 to 6 carbon atoms, alkenyl radicals containing 4 to 6 carbon atoms, phenyl radicals, cyano radicals, carboxy radicals, and alkyloxycarbonyl radicals whose alkyl portion contains 1 to 4 carbon atoms;
- a phenyl radical which is unsubstituted or substituted by at least one atom or radical selected from halogen atoms, alkyl radicals containing 1 to 4 carbon atoms, and alkyloxy radicals containing 1 to 4 carbon atoms; or a saturated or unsaturated nitrogen-containing heterocyclic radical containing 4 to 6 members and unsubstituted or substituted by at least one alkyl radical containing 1 to 4 carbon atoms; and
- G.sub.3 represents a group which protects the hydroxyl functional group;
- (b) reacting the formula (VIII) compound with a taxane derivative of the formula (IX): ##STR26## to obtain a product of formula X: ##STR27## wherein in formulae (IX) and (X), Ar, R.sub.3, G.sub.3 are defined as above, G.sub.1 represents a group which protects the hydroxyl functional group, and G.sub.2 represents an acetyl radical or a group which protects the hydroxyl functional group; and
- (c) replacing the groups G.sub.1 and G.sub.3 by hydrogen atoms, and replacing G.sub.2 by a hydrogen atom when G.sub.2 represents an hydroxyl-protecting group, to obtain a taxane compound of the formula (VII): ##STR28## in which Ar and R.sub.3 are defined as above and R.sub.2 represents a hydrogen atom or an acetyl radical.
- 4. The method according to claim 1 wherein G.sub.1 is selected from 2,2,2-trichloroethoxycarbonyl, trialkylsilyl, dialkylarylsilyl, alkyldiarylsilyl, or triarylsilyl radicals in which each alkyl portion contains 1 to 4 carbon atoms and each aryl portion represents a phenyl radical.
- 5. The method according to claim 1 wherein G.sub.2 is selected from an acetyl or 2,2,2-trichloroethoxycarbonyl radical.
- 6. The method according to claim 1 wherein G.sub.3 is selected from methoxymethyl, (1-ethoxy)ethyl, benzyloxymethyl, (.beta.-trimethylsilylethoxy)methyl, tetrahydropyranyl, 2,2,2-trichloroethoxymethyl, 2,2,2-trichloroethoxycarbonyl, anhydride, or mixed anhydride radicals, wherein the 2,2,2-trichloroethoxycarbonyl radical is optionally substituted in the form of a halide.
Priority Claims (1)
Number |
Date |
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92 02821 |
Mar 1992 |
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Parent Case Info
This is a continuation of application Ser. No. 08/295,677, filed as PCT/FR93/00224, Mar. 8, 1993, U.S. Pat. No. 5,608,102.
US Referenced Citations (5)
Foreign Referenced Citations (3)
Number |
Date |
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0 402 322 |
Dec 1990 |
EPX |
0 400 971 |
Dec 1990 |
EPX |
9113053 |
Sep 1991 |
WOX |
Non-Patent Literature Citations (2)
Entry |
I. Ojima et al., "Azetidines and Bisazetidines. Their Synthesis and Use as the Key Intermediates to Enantiomerically Pure Diamines, Amino Alcohols, and Polyamines", Journal of Organic Chemistry vol. 56, No. 18 (1991) pp. 5263-5277. |
Palomo et al. "Highly Steroselective Synthesis of alpha-hydroxy beta-Amino acids through beta-Lactams: Application to the Synthesis of the Taxol and Bestatin Side Chains and Related Systems", Tetrahedron Letters, vol. 31, No. 44. pp. 6429-6432, 1990. |
Continuations (1)
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