Claims
- 1. Process for the preparation of a .beta.-lactam of general formula: ##STR26## in which Ar' represents a phenyl or .alpha.- or .beta.-naphthyl radical which is optionally substituted with one or more atoms or radicals chosen from halogen atoms (fluorine, chlorine, bromine or iodine) and alkyl, alkenyl, alkynyl, aryl, arylalkyl, alkoxy, alkylthio, aryloxy, arylthio, hydroxyl, hydroxyalkyl, mercapto, formyl, acyl, acylamino, aroylamino, alcoxycarbonylamino, amino, alkylamino, dialkylamino, carboxyl, alkoxycarbonyl, carbamoyl, dialkylcarbamoyl, cyano, nitro and trifluoromethyl radicals, it being understood that the alkyl radicals and the alkyl portions of the other radicals contain 1 to 4 carbon atoms, that the alkenyl and alkynyl radicals contain 2 to 8 carbon atoms and that the aryl radicals are phenyl or .alpha.- or .beta.-naphthyl radicals, or alternatively Ar' represents a 5-membered aromatic heterocyclic radical containing one or more atoms, which may be identical or different, chosen from nitrogen, oxygen or sulphur atoms, and which is optionally substituted with one or more substituents, which may be identical or different, chosen from halogen atoms (fluorine, chlorine, bromine or iodine) and alkyl containing 1 to 4 carbon atoms, aryl containing 6 to 10 carbon atoms, alkoxy containing 1 to 4 carbon atoms, aryloxy containing 6 to 10 carbon atoms, amino, alkylamino containing 1 to 4 carbon atoms, dialkylamino in which each alkyl part contains 1 to 4 carbon atoms, acylamino in which the acyl part contains 1 to 4 carbon atoms, alkoxycarbonylamino containing 1 to 4 carbon atoms, acyl containing 1 to 4 carbon atoms, arylcarbonyl in which the aryl part contains 6 to 10 carbon atoms, cyano, carboxyl, carbamoyl, alkylcarbamoyl in which the alkyl part contains 1 to 4 carbon atoms, dialkylcarbamoyl in which each alkyl part contains 1 to 4 carbon atoms, or alkoxycarbonyl radicals in which the alkoxy part contains 1 to 4 carbon atoms, characterized in that the chirality-inducing group of a product of general formula: ##STR27## or of a mixture of products of general formula: ##STR28## in which R.sub.1 ' represents one or more substituents of which one must be in the ortho or para position, which are identical or different, and which are chosen from alkoxy containing 1 to 4 carbon atoms, alkylthio in which the alkyl part contains 1 to 4 carbon atoms or dialkylamino radical in which each alkyl part contains 1 to 4 carbon atoms, R.sub.2 ' represents an alkyl radical containing 1 to 4 carbon atoms and R.sub.3 ' represents an alkyl radical containing 1 to 4 carbon atoms, is replaced in order to obtain the product of general formula: ##STR29## or a mixture of products of general formula: ##STR30## in which Ar' and R.sub.2 ' are defined as above, which product is saponified in order to obtain the product of general formula: ##STR31## or a mixture of products of general formula: ##STR32## from which the product of general formula (Ia) is separated out by selective crystallization or by chiral phase chromatography.
- 2. Process according to claim 1, characterized in that replacement of the chirality-inducing group is carried out by hydrolysis in the presence of ammonium cerium nitrate or 2,3-dichloro-5,6-dicyano-p-benzoquinone or mercuric acetate or bis(trifluoroacetoxy)iodobenzene, by working in water or in an aqueous-organic medium at a temperature between 0 and 50.degree. C., or by electrochemical oxydation.
- 3. Process according to claim 2, characterized in that the solvent is chosen from nitriles and esters.
- 4. Process according to claim 1, characterized in that the saponification is carried out using ammonia dissolved in an aliphatic alcohol.
- 5. Process according to claim 1, characterized in that saponification of the mixture of products of general formula: ##STR33## in which Ar', R.sub.1 ', R.sub.2 ' and R.sub.3 ' are defined as above, is carried out in order to obtain a mixture of products of general formulae: ##STR34## in which Ar', R.sub.1 ' and R.sub.3 ' are defined as above, from which the constituent of general formula (VIa) is separated out, which is esterified using an acid of general formula:
- R.sub.2 '--CO--OH (VIIa)
- in which R.sub.2 ' is defined as above, in order to obtain the product of general formula: ##STR35## in which Ar', R.sub.1', R.sub.2 ' and R.sub.3 ' are defined as above, from which the chirality-inducing group is replaced in order to obtain the product of general formula: ##STR36## which is saponified in order to obtain the product of general formula (Ia).
- 6. Process according to claim 1, characterized in that the product of general formula (IIa) or the mixture of products of general formula (IIa) and (IIb) is obtained by the action of an acid halide of general formula: ##STR37## in which R.sub.2 ' is defined as in claim 1 and Hal represents a halogen atom, on a chiral imine of general formula: ##STR38## in which Ar', R.sub.1 ' and R.sub.3 ' are defined as in claim 1.
Priority Claims (2)
Number |
Date |
Country |
Kind |
92 02821 |
Mar 1992 |
FRX |
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93 04495 |
Apr 1993 |
FRX |
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Parent Case Info
This application is a Continuation-in-Part of application Ser. No. 08/697,420, filed Aug. 23, 1996, U.S. Pat. No. 5,763,628 which is a Continuation of application Ser. No. 08/295,677, filed Sep. 26, 1994, U.S. Pat. No. 5,608,102 Ser. No. 08/295,677 in a 371 of PCT/FR93/00224 filed Apr. 8, 1993. This application is also a Continuation-in-Part of application Ser. No. 08/537,728, filed Oct. 13, 1995, abandoned, in a 371 of PCT/FR93/00416, filed Apr. 14, 1994.
US Referenced Citations (5)
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Dec 1990 |
EPX |
0 400 971 A2 |
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EPX |
0525589 A1 |
Feb 1993 |
EPX |
9113053 |
Sep 1991 |
WOX |
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Entry |
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Ojima et al., "New and Efficient Approaches to the Semisynthesis of Taxol and its C-13 Side Chain Analogs by Means of .beta.-Lactam Synthon Method", Tetrahedron vol. 48, (1992) pp. 6985-7012. |
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Ojima et al., "Efficient and Practical Asymmetric Synthesis of the Taxol C-13 Side Chain, N-Benzoyl-(2R, 3S)-3-phenylisoserine, and Its Analogues via Chiral 3-Hydroxy-4-aryl-.beta.-lactams through Chiral Ester Enolate-Imine Cyclocondensation", J. Org. Chem., vol. 56 (1991) pp. 1681-1683. |
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Related Publications (1)
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537728 |
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Continuation in Parts (1)
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Number |
Date |
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Parent |
697420 |
Aug 1996 |
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