http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-701803-A

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Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_571b8abacacea64d3f7089d0983b8b3b
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07B2200-07
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C225-16
filingDate 1951-02-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d59e6f6dbf13f100dee8fc147b6407d5
publicationDate 1954-01-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-701803-A
titleOfInvention Diphenyl ketones of pharmaceutical value and the preparation thereof
abstract The invention comprises the compounds 6-ethylmethylamino-5-methyl-4, 4-diphenylhexan-3-one and 6-ethylmethylamino-4, 4-diphenylheptan-3-one, and their salts. The compounds are analgesics and may be prepared by treating 3-ethylmethylamino-2-methyl-1, 1-diphenyl-propyl cyanide or 3-ethylmethylamino-1, 1-diphenylbutyl cyanide, respectively, with ethyl magnesium bromide. In examples, ethylmethylamine is heated with propylene oxide to give 1-ethylmethylamino-2-propanol which is reacted with thionyl chloride in chloroform to yield 1-ethylmethylamino-2-chloropropane; this is then refluxed with diphenylmethyl cyanide and sodamide in benzene to produce a mixture of the isomers 3-ethylmethylamino-1, 1-diphenylbutyl cyanide and 3-ethylmethylamino-2-methyl-1, 1-diphenylpropyl cyanide. After separation, these compounds are reacted with ethyl magnesium bromide according to the Grignard process. The oxalate and the hydroiodide of 6-ethylmethylamino-5-methyl-4, 4-diphenylhexan-3-one, and the hydrobromide of 6-ethylmethylamino-4, 4-diphenylheptan-3-one are described. The Provisional Specification refers to Specifications 654,975, 677,522 and 688,481.
priorityDate 1951-02-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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