http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2011201807-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_005fecba76415a8c346c2f2de80e4b33
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P3-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P43-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D207-416
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D207-416
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-20
filingDate 2011-04-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_24533f5d2e252d12d781856b3a60964c
publicationDate 2011-08-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2011201807-A1
titleOfInvention 3-hydrazino-2,5-dioxopyrrolidine-3-carboxylate, process for production of the same, and use of the same
abstract The present invention provides 3-hydrazino-2,5-dioxopyrrolidine-3-carboxylates of the formula (I): n n n n n n n n n n wherein R 1 is a C 1-6 alkyl group, etc., R 2 is a hydrogen atom or a COOR 3 group, wherein R 3 is a tert-C 4-6 alkyl group, a 2,2,2-trichloroethyl group or a benzyl group in which the benzene ring moiety may be optionally substituted by one or two atoms or groups independently selected from the group consisting of a halogen atom, a C 1-4 alkyl group, a C 1-4 alkoxy group, a cyano group and a nitro group, and a salt thereof, which are useful as a novel intermediate for preparing tetrahydropyrrolo[1,2-a]pyrazin-4-spiro-3′-pyrrolidine derivatives such as Ranirestat being promising therapeutic agents for diabetic complications in a short process and in an economically advantageous and safe manner, and the process for preparing the same.
priorityDate 2006-07-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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