发明授权
US5550230A 7-Substituted-2-oxa-7-azabicyclo [3.2.0.]heptan-6-one compound and
method for the preparation thereof
失效
7-取代-2-氧杂-7-氮杂双环[3.2.0]庚-6-酮化合物及其制备方法
- 专利标题: 7-Substituted-2-oxa-7-azabicyclo [3.2.0.]heptan-6-one compound and method for the preparation thereof
- 专利标题(中): 7-取代-2-氧杂-7-氮杂双环[3.2.0]庚-6-酮化合物及其制备方法
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申请号: US396778申请日: 1995-03-01
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公开(公告)号: US5550230A公开(公告)日: 1996-08-27
- 发明人: Yoichi Taguchi , Akihiro Oishi , Isao Shibuya , Tohru Tsuchiya
- 申请人: Yoichi Taguchi , Akihiro Oishi , Isao Shibuya , Tohru Tsuchiya
- 申请人地址: JPX
- 专利权人: Japan as represented by Director General of Agency of Industrial Science and Technology
- 当前专利权人: Japan as represented by Director General of Agency of Industrial Science and Technology
- 当前专利权人地址: JPX
- 优先权: JPX6-65500 19940308
- 主分类号: A01N43/90
- IPC分类号: A01N43/90 ; C07D491/04 ; C07D491/048 ; A61K31/395
摘要:
Disclosed is a novel .beta.-lactam compound, a 7-substituted-2-oxa-7-azabicyclo[3.2.0]heptan-6-one represented by the general formula ##STR1## in which R is an alkyl, cycloalkyl, aryl, halogen-substituted aryl or alkaryl group, having usefulness as an intermediate for the synthesis of various biologically active compounds. The compound can be prepared by the reaction of an isocyanate compound RNCO, R being the same as above, and 2,3-dihydrofuran, preferably, under pressurization up to 2000 atmospheres or higher.
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