The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.
The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.
Patent No.:
Date of Patent:
Sep. 11, 2012
Filed:
Aug. 13, 2008
Kimihiko Goto, Yokohama, JP;
Kazumi Yamamoto, Kamakura, JP;
Masayo Sakai, Yokohama, JP;
Masaaki Mitomi, Yokosuka, JP;
Takashi Ando, Yokohama, JP;
Kimihiko Goto, Yokohama, JP;
Kazumi Yamamoto, Kamakura, JP;
Masayo Sakai, Yokohama, JP;
Masaaki Mitomi, Yokosuka, JP;
Takashi Ando, Yokohama, JP;
Meiji Seika Pharma Co., Ltd., Tokyo-To, JP;
Abstract
Disclosed is a process for producing compound C represented by formula C: wherein R' represents straight chain, branched chain, or cyclic Calkylcarbonyl, wherein Ris used as a protective group for hydroxyl at the 7-position of compound C. Rrepresents formyl; optionally substituted straight chain Calkylcarbonyl; optionally substituted benzyl; group —SiRRRoptionally substituted by halogen atom wherein R, R, and Reach independently represent straight chain or branched chain Calkyl or phenyl; Calkyloxy-Calkyl optionally substituted by halogen atom; Calkylthio-Calkyl optionally substituted by halogen atom; straight chain, branched chain, or cyclic Calkyl optionally substituted by halogen atom, provided that, when alkyl in the Calkyl group is of a branched chain or cyclic type, the alkyl group is Calkyl; Calkenyl optionally substituted by halogen atom; Calkynyl optionally substituted by halogen atom; or an optionally substituted saturated or unsaturated five- or six-membered heterocyclic group. The process can produce pyripyropene derivatives that have acyloxy groups at the 1- and 11-positions and a hydroxyl group at the 7-position and are useful as insect pest control agents at a high yield.