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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D265-26
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D265-26
filingDate 1975-08-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1977-03-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6fa58174329fcee817b319f7511212a9
publicationDate 1977-03-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4013646-A
titleOfInvention 1-(ω-HALOALKYL)-ISATOIC ANHYDRIDES
abstract CNS depressants of the formulae IA and IB: ##STR1## in which n and p are each 0 or 1, Z - is an anion and R 1 , R' 1 , R 2 , R' 2 , R 3 and R 4 are optional substituents. Compounds IB may be prepared by reducing compounds IA which may be made by reacting a N-(ω-haloalkyl) isatoic anhydride with a cyclic pseudothiourea such as a 2-organomercapto-4,5-dihydroimidazole. Compounds IB may be also prepared by cyclizing a 1-(ω-haloalkyl)-2,3-dihydro-imidazo[2,1-b]quinazolin-1H-5-one. The compounds are anti-inflammatory, analgesic and immunosuppressant agents.
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