发明授权
US08975403B2 Process for producing substituted benzo[F]imidazo[1,2-A]quinoxalin-3(11H)-ones
有权
取代苯并[F]咪唑并[1,2-A]喹喔啉-3(11H)酮的制备方法
- 专利标题: Process for producing substituted benzo[F]imidazo[1,2-A]quinoxalin-3(11H)-ones
- 专利标题(中): 取代苯并[F]咪唑并[1,2-A]喹喔啉-3(11H)酮的制备方法
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申请号: US14189706申请日: 2014-02-25
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公开(公告)号: US08975403B2公开(公告)日: 2015-03-10
- 发明人: Satoshi Inouye , Yuiko Miura , Suguru Yoshida , Takamitsu Hosoya
- 申请人: JNC Corporation , National University Corporation Tokyo Medical and Dental University
- 申请人地址: JP Tokyo JP Tokyo
- 专利权人: JNC Corporation,National University Corporation Tokyo Medical and Dental University
- 当前专利权人: JNC Corporation,National University Corporation Tokyo Medical and Dental University
- 当前专利权人地址: JP Tokyo JP Tokyo
- 代理机构: Drinker Biddle & Reath LLP
- 优先权: JP2011-050487 20110308
- 主分类号: C07D241/36
- IPC分类号: C07D241/36 ; C07D487/04 ; C07D241/38 ; C07D241/44 ; C07D241/54
摘要:
A simple process for producing v-coelenterazine compounds has been desired. Described is a process for producing a v-coelenterazine compound represented by general formula (II) comprising (1) the step of reacting a compound of general formula (VIII) with a methyltriphenylphosphonium salt in the presence of a base to give a compound represented by general formula (IX), (2) the step of performing a ring-closing metathesis reaction on any one selected from the group consisting of the compound represented by general formula (IX) and a compound of general formula (X) which is the compound of general formula (IX) wherein the amino is protected with R5, and then deprotecting R4 and, if any, R5 to give a v-coelenteramine compound represented by general formula (XIV), and (3) the step of reacting the compound of general formula (XIV) with a compound represented by general formula (XV) to give the compound of general formula (II).
公开/授权文献
- US20140206868A1 PROCESS FOR PRODUCING v-COELENTERAZINE COMPOUNDS 公开/授权日:2014-07-24
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