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filingDate 1988-03-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8101e46de1b76a9b6281859d68f71a6c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_547e936a662e5c775c5c4bd2c3e124d0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d0d4c2872e0185542e29bfc602d7ed7d
publicationDate 1990-12-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber HU-201757-B
titleOfInvention Process for producing pyrroloquinoline-, acridine-, benzoxazine-, benzthiazine-, indolobenzoxazine-, benzazepine and pyrrolophenothiazine carboxamides and pharmaceutical compositions comprising same
abstract Compounds of the formulan wherein the broken line represents an optional double bond; X is O, S, CH₂ or CH₂CH₂; R¹ is selected from the group consisting of hydrogen, halogen, C₁-C₆ alkoxy, C₁-C₆ alkanoyl, C₁-C₆ alkyl, and C₁-C₆ alkyl substituted with 1, 2 or 3 halogen atoms; R² is selected from the group consisting of phenyl, substituted phenyl, heterocyclic groups, and substituted heterocyclic groups, said substituted phenyl and substituted heterocyclic groups being substituted with 1 or 2 substituents independently selected from the group consisting of C₁-C₆ alkyl, trifluoromethyl, and halogen; nR³ and R⁴ are independently selected from the group consisting of hydrogen, halogen, C₁-C₆ alkyl, or trifluoromethyl, or R³ and R⁴, taken together with the carbon atoms to which they are attached, form a six-membered carbocyclic aromatic ring, said aromatic ring being optionally substituted with one or two substituents selected from the group consisting of halogen, C₁-C₆ alkyl, and C₁-C₆ alkyl substituted with 1, 2 or 3 halogen atoms; and the pharmaceutically acceptable salts thereof. The compounds are useful in treating inflammation or other prostaglandin or leukotriene mediated diseases.
priorityDate 1988-03-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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