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filingDate 1981-07-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1984-11-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_31249af74125c79c99d2aafd6664c2fd
publicationDate 1984-11-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber SU-1124888-A3
titleOfInvention Method of obtaining derivatives of 5-substituted oxazolidine-2,4-diones in form of racemate or optically active isomer in free state or in form of pharmaceutically acceptable salt
abstract The method of producing 5-substituted oxazolidine-2,4-dion derivatives of the general formula I R Y V ° o -H-RI where R is a hydrogen atom, acetyl, C -Cj-alkylcarbamoyl, cyclohexylcarbamoyl or C -C alkoxycarbonyl; RI is a group of formula where Z is a chlorine atom or trifluoromethyl; Z is a chlorine atom, methyl, C-Cd-Alft} rmethyl; Z "a hydrogen or halogen atom, methyl or C -C-alkoxyl; Z is a hydrogen or halogen atom, methyl, and a nitro group or an alkoxy, provided that when R is a hydrogen atom, 2 is different - the photon of a hydrogen atom, and Z and Z. together are not methyl; 7 -fc a hydrogen or fluorine atom, or a nitro group; U-, hydrogen or fluorine atom; 1, C-C - alkoxy or methyl, benzyloxy group; a y, hydrogen or methoxyl, C as a paramame or optically active izscher in free form or as a pharmaceutically acceptable salt, and when R is a hydrogen atom, characterized in that the compound of general formula II 1C BUT KNy - OR 00 00 00 R, S where RJ roieeT is the indicated value; R J - C -Cj-alkyl, is reacted with phosgene in an inert organic solvent medium and the resulting compound of the general formula III O n O I and OR, R
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2012112708-A1
priorityDate 1981-01-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID160311385

Total number of triples: 294.