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Title:
AZETIDINONE COMPOUND
Document Type and Number:
Japanese Patent JPS5955888
Kind Code:
A
Abstract:

NEW MATERIAL:The compound of formula I [R1 is (substituted) phenyl; R2 is carboxyl-protecting group; X is H or Cl; Y is I, ONO2, OH, group of formula IIWIV, or SR4; R3 is lower alkyl or OR5 (R5 is halogen-containing lower alkyl); R4 is (substituted) S- or N-containing 5-membered hetrocyclic group].

EXAMPLE: 2-( 3-Phenyldichloromethyl- 7- oxo-4-thia-2, 6-diazabicyclo[ 3,2,0 ]-hept- 2-en-6-yl)-3-ethoxythiocarbonylthiomethyl-3-butenoic acid methyl ester.

USE: Synthetic intermediate of cephalosporin-type antibiotic substance useful as an antibacterial agent.

PROCESS: The compound of formula V is made to react with the nucleophilic agent of formula M-Y (M is Na or K; Y is I or group of formula III) in an organic solvent such as acetone, dimethyl sulfoxide, etc. preferably at 10W55°C for 0.5W4hr.


Inventors:
TORII SHIGERU
TANAKA HIDEO
NOGAMI JIYUNZOU
SASAOKA MICHIO
SHIROI TAKASHI
SAITOU NORIO
Application Number:
JP16705182A
Publication Date:
March 31, 1984
Filing Date:
September 24, 1982
Export Citation:
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Assignee:
OTSUKA KAGAKU YAKUHIN
International Classes:
C07D501/30; C07D501/36; C07D501/42; C07D501/52; C07D513/04; (IPC1-7): C07D513/04
Domestic Patent References:
JPS5759896A1982-04-10
JPS5143791A1976-04-14
Attorney, Agent or Firm:
Eiji Saegusa



 
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