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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D295-112
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C49-83
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C46-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D295-112
filingDate 1969-11-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1971-11-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6ab22d4bf6045aa5058cd6b7253bb3a3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_02346d87864962766f935728bebfe50c
publicationDate 1971-11-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-3621062-A
titleOfInvention 2-(8-cyclohexyloctanoyl or 7-cyclohexylheptanoyl)-1-naphthol
abstract Intermediates for the preparation of 2-hydroxy-3-(8cyclohexyloctyl)-1,4-naphthoquinone and 2-hydroxy-3-(7cyclohexylheptyl)-1,4-naphthoquinone, potent antimalarial agents, are prepared as follows: reacting 8-cyclohexyloctanoic acid or 7cyclohexylheptanoic acid with 1-naphthol to form 2-(8cyclohexyloctanoyl or 7-cyclohexylheptanoyl)-1-naphthol; reducing the 2-acyl-1-naphthol to form 2-(8-cyclohexyloctyl or 7cyclohexylheptyl)-1-naphthol; oxidizing 2-(8-cyclohexyloctyl or 7-cyclohexylheptyl)-1-Napthol to form 2-(8-cyclohexyloctyl or 7cyclohexylheptyl)-1,4-naphthoquinone; reacting the latter with a peroxide under alkaline conditions to form 2-(8-cyclohexyloctyl or 7-cyclohexylheptyl)-1,4-naphthoquinone-2,3-oxide; and, hydrolyzing the 2,3-oxide under acidic conditions to yield 2hydroxy-3-(8-cyclohexyloctyl or 7-cyclohexylheptyl)-1,4naphthoquinone.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2008125411-A1
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priorityDate 1966-10-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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