摘要 |
<p>The present invention provides a process for preparing a cephem derivative characterized in that an allenyl beta -lactam compound represented by the formula (1) <CHEM> wherein R<1> is amino or protected amino, R<2> is a hydrogen atom or lower alkoxyl, R<3> is a hydrogen atom or carboxylic acid protecting group and X is the group -SO2R<4> or -SR<4>, R<4> being substituted or unsubstituted aryl or substituted or unsubstituted nitrogen-containing aromatic heterocyclic group is reacted with a nucleophilic agent to obtain the derivative, the cephem derivative being represented by the formula (2) <CHEM> wherein R<1>, R<2> and R<3> are as defined above, and Y is the residue of the nucleophilic agent.</p> |
申请人 |
OTSUKA KAGAKU K.K., OSAKA, JP |
发明人 |
TORII, SIGERU, AKAIWA-GUN, OKAYAMA-KEN, JP;TANAKA, HIDEO, OKAYAMA-SHI, OKAYAMA-KEN, JP;TANIGUCHI, MASATOSHI, C/O OTSUKA KAGAKU K.K., OSAKA-SHI, OSAKA-FU, JP;SASAOKA, MICHIO, C/O OTSUKA KAGAKU K.K., TOKUSHIMA-SHI, TOKUSHIMA-KEN, JP;SHIROI, TAKASHI, C/O OTSUKA KAGAKU K.K., TOKUSHIMA-SHI, TOKUSHIMA-KEN, JP;KAMEYAMA, YUTAKA, C/O OTSUKA KAGAKU K.K., TOKUSHIMA-SHI, TOKUSHIMA-KEN, JP |