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http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D213-53
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-53
filingDate 1979-12-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1981-01-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a13e5e465cc048f773a4e774cae64610
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ba8e0b00a465abb1cfd5c019d7732b73
publicationDate 1981-01-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4246420-A
titleOfInvention Process for preparing 3-(4-pyridinyl)-2-cyclohene-1-oxime
abstract An improved method of preparing 3-(4-pyridinyl)-2-cyclohexen-1-one oxime from ethyl 5-oxo-2-[(4-pyridinyl)-carbonyl]hexanoate is a one pot sequence which comprises first heating ethyl 5-oxo-2-[(4-pyridinyl)carbonyl]hexanoate with excess sulfuric acid, neutralizing the excess acid, extracting the resulting 3-(4-pyridinyl)-2-cyclohexen-1-one with isopropyl alcohol, draining off the heavier aqueous layer, adding hydroxylamine hydrochloride to the isopropyl alcohol solution of said 2-cyclohexen-1-one, stirring the mixture at reflux, basifying the mixture and evaporating it to dryness, and isolating 3-(4-pyridinyl)-2-cyclohexen-1-one oxime from the residue. The oxime is an intermediate for preparing 3-(4-pyridinyl)aniline, in turn, an intermediate for preparing rosoxacin, an antibacterial agent.
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