发明名称 CEPHALOSPORIN ANALOGUE
摘要 <p>NEW MATERIAL:The titled compound of formula I [X is halogen; R1 is H or aliphatic hydrocarbon residue (the substituent group is selected from carboxy, etc.); R2 is H, lower alkyl, etc.; R3 is carboxy]. EXAMPLE:( + or - )-cis-7-( 4-Bromo-3-oxo-2-methoxyiminobutyrylamino )-1-azabicyclo [4,2,0]oct-2-en-8-one-2-carboxylic acid. USE:Antibacterial agent, disinfectant, etc. PROCESS:The compound of formula I can be prepared by condensing the compound of formula III or its reactive derivative (e.g. acid halide, etc.) with the compound of formula IV, its salt or its equivalent (called generally as 7-amino compounds), and if necessary, eliminating the protecting group of R3 by conventional method, and further converting to a proper salt.</p>
申请公布号 JPS5649380(A) 申请公布日期 1981.05.02
申请号 JP19790124887 申请日期 1979.09.28
申请人 KYOWA HAKKO KOGYO KK 发明人 HIRATA TADASHI;MATSUSHIMA HIDEO;OGASA TAKEHIRO
分类号 C07D463/00;A61K31/435;A61P31/04;C07D471/04 主分类号 C07D463/00
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