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http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D513-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P25-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D277-56
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D277-56
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D277-20
filingDate 1989-08-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_42a1907e90ab49beeed5d2e1963f86fd
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fbbe8c71234659b601d8fa9759f183d5
publicationDate 1995-05-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber PT-91401-B
titleOfInvention PROCESS FOR THE PREPARATION OF BENZODIAZEPINE COMPOUNDS
abstract Pharmaceutical thiazolo-[1,5]benzodiazepines of the formulan in which R¹, R², R³ and R⁴ are independently hydrogen, C₁₋₄ alkyl, C₂₋₄ alkenyl, halogen, C₁₋₄ haloalkyl, nitro, C₁₋₄ alkoxy, C₁₋₄ haloalkoxy, C₁₋₄ alkylthio or phenylsulphonyl; in which R⁵ is a group of the formula formulan where R⁷ is hydrogen, C₁₋₆ alkyl, C₃₋₇ cycloalkyl C₁₋₄ alkyl, benzyl or ZO-C₂₋₆ alkyl where Z is hydrogen or an acyl group, R⁸ is hydrogen or C₁₋₄ alkyl and n is 0 or 1, provided that when R⁷ is hydrogen n is 0; in which R⁶ is hydrogen, C₁₋₁₀ alkyl, C₃₋₇ cycloalkyl, C₃₋₇ cycloalkyl C₁₋₄ alkyl, C₁₋₄ haloalkyl, C₁₋₄ alkoxy or C₁₋₄ alkylthio; and in whichn represents a thiazole ring selected fromn and acid addition salts thereof. n The compounds have central nervous system activity.
priorityDate 1988-08-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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