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Title:
PREPARATION OF 3-METHYLENECEPHAM COMPOUND OR ITS SALT
Document Type and Number:
Japanese Patent JPS58222092
Kind Code:
A
Abstract:

PURPOSE: To obtain the titled compound useful as an intermediate for a 3- cephem compound having antibacterial activity in high purity in high yield, by reducing a cephemcarboxylic acid derivative having thiomethyl at 3-position with a combination of a metal and an ammonium salt of an acid.

CONSTITUTION: A cephemcarboxylic acid derivative shown by the formula I [R1 is (protected)amino; R2 is (protected)carboxy; R3 is halogen, (substituted)heterocyclic thio] having thiomethyl at 3-position is reduced with a combination of a metal (e.g., zine, etc.) and an ammonium salt (e.g., ammonium halide such as ammonium chloride, etc.) of an acid, to give 3-methylcepham compound shown by the formula II. The reaction is preferably carried out in a solvent such as N,N-dimethylformamide, etc. in the presence of urea.


Inventors:
TAKATANI TAKAO
MASUGI TAKASHI
CHIBA TOSHIYUKI
YOSHIOKA AKITERU
UEDA IKUO
KOBAYASHI MASAKAZU
KATOU MASAYUKI
Application Number:
JP10570482A
Publication Date:
December 23, 1983
Filing Date:
June 18, 1982
Export Citation:
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Assignee:
FUJISAWA PHARMACEUTICAL CO
International Classes:
C07D501/04; C07B61/00; C07D501/22; (IPC1-7): C07D501/04
Domestic Patent References:
JPS50105682A1975-08-20
JPS4720188A
Attorney, Agent or Firm:
Aoki High