Process for producing optically active...

Organic compounds -- part of the class 532-570 series – Organic compounds – Heterocyclic carbon compounds containing a hetero ring...

Reexamination Certificate

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Reexamination Certificate

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10952167

ABSTRACT:
An optically active N-protected azetidine-2-carboxylic acid (5) can be produced by preparing an optically active 4-amino-2-halobutyric acid (3)by halogenating an optically active 3-hydroxy-2-pyrrolidinone (1) with inversion of configuration to prepare an optically active 3-halo-2-pyrrolidinone (2) followed by hydrolysis orby halogenating an optically active 4-amino-2-hydroxybutyric acid ester (6) with inversion of configuration to prepare an optically active 4-amino-2-halobutyric acid ester (7) followed by hydrolysis orby halogenating the compound (6) with inversion of configuration to prepare the compound (7), cyclizing the same to prepare the compound (2) followed by hydrolysis,further cyclizing the compound (3) followed by treating the reaction product with an amino group-protecting agent. The thus-obtained compound (5) can be improved its optical purity further by recrystallization

REFERENCES:
patent: 3853888 (1974-12-01), Roman
patent: 6313315 (2001-11-01), Yamauchi et al.
patent: 257602 (1987-08-01), None
patent: 257602 (1988-03-01), None
patent: 393 441 (1990-10-01), None
patent: 393441 (1990-10-01), None
patent: 844 242 (1998-05-01), None
patent: 844242 (1998-05-01), None
patent: 855 446 (1998-07-01), None
patent: 855446 (1998-07-01), None
patent: 48-052721 (1973-07-01), None
patent: 48-052721 (1973-07-01), None
patent: 49-11844 (1974-02-01), None
patent: 49-011844 (1974-02-01), None
patent: 49-11844 (1974-02-01), None
patent: 49-054532 (1974-05-01), None
patent: 49054532 (1974-05-01), None
patent: 60-120888 (1985-06-01), None
patent: 60-120888 (1985-06-01), None
patent: 61-085392 (1986-04-01), None
patent: 61-085392 (1986-04-01), None
patent: 63-060954 (1988-03-01), None
patent: 63-060954 (1988-03-01), None
patent: 04-095067 (1992-03-01), None
patent: 04-095067 (1992-03-01), None
patent: 08-119935 (1996-05-01), None
patent: 08-119935 (1996-05-01), None
J. Med. Chem., 1997, vol. 30, No. 11, pp. 1995-1998.
J. Med. Chem., 1996, vol. 39, No. 4, pp. 817-825.
J. Antibiol., 1990, vol. 430, No. 7., pp. 858-872.
Ikuta, H., et al., “Synthesis and Antiinflammatory Activities of 3-(3,5-Di-tert-butyl-4-hydroxybenzylidene) pyrrolidin-2-ones,”J. Med. Chem., vol. 30, No. 11, Nov. 1987, pp. 1995-1998.
Abreo, M.A., et al., “Novel 3-Pyridyl Ethers with Subnanomolar Affinity for Central Neuronal Nicotinic Acetylcholine Receptors,”J. Med. Chem., vol. 39, No. 4, Feb. 16, 1996, pp. 817-825.
Hoshi, H., et al., “Amikacin Analogs with a Fluorinated Amino Acid Side Chain,”J. Antibiotics, vol. 43, No. 7, Jul. 1990, pp. 858-872.
Yamada, et al. “Synthesis of (+−)-Azetidine-2carboxylic Acid and 2-Pyrrrolidone Derivatives”,Agricultural and Biological Chemistry, 1973, vol. 37, No. 3, pp. 649-652.

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