发明名称 |
Process for preparing carbapenem compounds |
摘要 |
Novel amino acid derivatives of the formula <IMAGE> wherein R1 is a protecting group removable under reducing or acid conditions, and R2 and R5 are hydrogen or carboxylic protecting groups, are useful as intermediates in preparing stereospecific carbapenam/carbapenem derivatives. R1 is removed under reducing conditions to form a pyrrolidine derivative, which is further cyclized from the R5=H compound to form a beta -lactam ring. Stereospecificity at the 6-position is achieved by treatment with lithium diisopropylamide (LDA) and quenching at different temperatures. Compound (I) can be prepared by treating R1-protected R3-pyrrolidone carboxylic acid R2-ester with a lithium enolate of the formula R4CHLiCO2R5. The lithium enolate can be formed from R4CH2CO2R5 by treatment with LDA.
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申请公布号 |
US5204459(A) |
申请公布日期 |
1993.04.20 |
申请号 |
US19920853069 |
申请日期 |
1992.03.17 |
申请人 |
AJINOMOTO CO., INC. |
发明人 |
NOZOE, SHIGEO;OHTA, TOMIHISA |
分类号 |
C07C271/22;C07D207/16;C07D477/04 |
主分类号 |
C07C271/22 |
代理机构 |
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