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Title:
2-ALKYLCYSTEINAMIDE OR SALT THEREOF, PROCESS FOR PRODUCING THESE, AND USE OF THESE
Document Type and Number:
WIPO Patent Application WO/2004/090152
Kind Code:
A1
Abstract:
A process for producing a 2-alkylcysteinamide represented by the general formula (1) or a salt thereof, which comprises hydrolyzing a 4-alkylthiazolidine-4-carboxamide represented by the general formula (2) or a salt thereof. (In the general formula (1), R represents C1-4 alkyl.) (In the general formula (2), R represents C1-4 alkyl; and R1 and R2 each independently represents hydrogen or C1-4 alkyl or R1 is bonded to R2 to form a C4-7 alicyclic structure, provided that not both of R1 and R2 are hydrogen.) Either cells of a microorganism having the ability to stereoselectively hydrolyzing a 2-alkyl-L-cysteinamide or a substance obtained by treating the cells is caused to act on the compound of the general formula (1) to yield a 2-alkyl-L-cysteine.

Inventors:
HIGUCHI YASUSHI (JP)
TANAKA AKINORI (JP)
HASEMI RYUJI (JP)
Application Number:
PCT/JP2004/004988
Publication Date:
October 21, 2004
Filing Date:
April 07, 2004
Export Citation:
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Assignee:
MITSUBISHI GAS CHEMICAL CO (JP)
HIGUCHI YASUSHI (JP)
TANAKA AKINORI (JP)
HASEMI RYUJI (JP)
International Classes:
C07C319/02; C07C319/06; C07C323/60; C12P13/12; C12P41/00; (IPC1-7): C12P41/00
Foreign References:
JP2001328970A2001-11-27
JP2002315597A2002-10-29
JPS5714573A1982-01-25
Other References:
BRANT L. ET AL: "Thiazoline ring formation from 2-methylcysteines and 2-halomethylalanines", HETEROCYCLES, vol. 58, 2002, pages 601 - 634, XP002980831
DUNKERTON L.V.: "Synthesis of potential anti-vesicant compounds", AD REP., vol. AD-B-161803, 1992, pages 1 - 49, XP002980829
Attorney, Agent or Firm:
Ide, Masatake (9F Gobancho Grand Bldg., 3-1, Gobanch, Chiyoda-ku Tokyo, JP)
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