http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-3720714-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_3a5173a7d063a9f70ca7b5e86fc23863
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C43-1742
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C59-64
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C259-14
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C59-64
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C43-174
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C259-14
filingDate 1970-10-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1973-03-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_91761eb82a02f0f36095e0f859516e9d
publicationDate 1973-03-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-3720714-A
titleOfInvention 2-alkoxy-2(naphthyl)-alkanamidoximes
abstract A 2-(lower-alkoxy)-2-Ar alkanamidoxime, having hypoglycemic activity, where Ar is phenyl, naphthyl, indanyl, biphenylyl, cyclohexenyl, cyclohexyl or phenyl substituted by from one to three substituents selected from lower-alkyl, lower-alkoxy, halo, trihalomethyl, lower-alkylmercapto, lower-alkylsulfonyl, di(lower-alkyl)amino, amino, hydroxy, nitro or benzyloxy, is prepared by reacting a 2-(lower-alkoxy)-2-Ar-alkanenitrile with hydroxylamine. The intermediate 2-(lower-alkoxy)-2-Aralkanenitrile is prepared preferably by first reacting Ar-CHO with a tri-(lower-alkyl) orthoformate to form the aldehyde di(lower-alkyl) acetal, reacting the latter with an acyl halide to form the corresponding Alpha -halo-Ar-methyl lower-alkyl ether and reacting said ether with an alkali cyanide to yield said intermediate nitrile.
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4339584-A
priorityDate 1968-06-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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