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Title:
CEPHALOSPORIN DERIVATIVE
Document Type and Number:
Japanese Patent JPS58180491
Kind Code:
A
Abstract:

NEW MATERIAL:A compound(salt) shown by the formula I [R1 is α-aminoacyl, dipeptidyl consisting of an α-amino acid, etc.; R2 is group shown by the formula II(R5 and R6 are H, lower alkyl, or R5 and R6 are linked to form a ring consisting of methylene chain; X is H, lower alkyl, carboxy, etc.); R3 is H, methyl, chlorine, methoxy, etc.; R4 is H, or ester residue].

EXAMPLE: 7-[(Z)-2-(2-L-Alanylamino-4-thiazolyl)-2-methoxyimino-acetamido]-3-methyl-3-caphem-4-carboxylic acid.

USE: A preventive and remedy for microbism.

PROCESS: For example, the amino group of a compound shown by the formula III(R7 is ester residue) is protected and hydrolyzed to give a carboxylic acid derivative, which is reacted with a 7-amino-cephalosporin shown by the formula IVto give a reaction product whose amino-protecting group is removed to give a compound shown by the formula I .


Inventors:
FUKATSU HIROSHI
NAKAGAWA SUSUMU
IWATSUKI IKUO
IWADARE SHIYUUICHI
Application Number:
JP6236782A
Publication Date:
October 21, 1983
Filing Date:
April 16, 1982
Export Citation:
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Assignee:
BANYU PHARMA CO LTD
International Classes:
C07D501/20; A61K31/545; A61K31/546; A61P31/04; C07D501/59; (IPC1-7): A61K31/545; C07D501/20; C07D501/59