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filingDate 1979-10-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2d9e40ae2de6784c1ce22ee8fdcc4a72
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publicationDate 1981-05-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S5655400-A
titleOfInvention Improved preparation process of 4,6-dien-3-one steroid
abstract PURPOSE: To prepare the titled compound useful as an intermediate of active corpus luteum hormone, antiandrosterone diuretic, hypotensive agent, etc., economically, in an industrial scale, by the bromination and then dehydrobromination reaction of an enol ether of a specific steroid under specific conditions. n CONSTITUTION: An enol ether of a steroid wherein the 3, 4, 5, and 6-positions of the A- and B-rings are group of formula I (X 1 is H, methyl, F, Cl or Br; R 1 is 1W3C alkyl) is brominated with a halogenating agent capable of supplying positive bromine ions, in a water-containing organic solvent free of acetic acid and sodium acetate to obtain 6-bromosteroid of formula II, which is subjected to the debromination in a solvent containing DMF or N-methylpyrrolidone by reacting directly with lithium halide and an inorganic carbonate maintaining the water contact in the solvent to 1W9wt% to obtain the objective compound of formula III. n COPYRIGHT: (C)1981,JPO&Japio
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2002241395-A
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