http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2002105076-A

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filingDate 2001-07-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cf8f152f1318a08e556bc782259fc330
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publicationDate 2002-04-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2002105076-A
titleOfInvention Pyrazolo [4,3-d] pyrimidin-7-one compounds and methods for producing intermediates thereof
abstract (57) [Summary]n[PROBLEMS] Mostly type 5 cyclic guanosine 3 ', 5'-monophosphate phosphodiesterase (cGMP PD E5) is an inhibitor of various therapeutic fields (male erectile function) Series of pyrazolo [4,3-d] useful in A pyrimidin-7-one compound is provided.nSOLUTION: Formula (I):nEmbedded imagen Or a pharmaceutically or veterinarily acceptable compound thereof Functional salts, prodrugs, polymorphs and / or solvates A process for producing a compound of formula (II), (II) I), (IV) or (V):nEmbedded imagen Embedded imagen (Each compound is defined in claim 1 of this specification) Is -OR) Three And in the presence of hydroxide scavengers Or a compound of the formula (IV) or (V) In the case of the compound of the above, the auxiliary base and the hydroxide scavenger That is, -OR Three Is substituted with the auxiliary base) It is a method including reacting in the presence.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2009530256-A
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priorityDate 2000-07-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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