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filingDate 1990-12-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6b161fa74f033f9825e2c12fd7b05753
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publicationDate 1992-04-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H04103581-A
titleOfInvention 5-(1-imidazol)methyl)-3,3-disubstituted-2(3h)furanone derivative
abstract NEW MATERIAL: A compound of the formula (the dotted line indicates the 4,5-unsaturated of the 4,5-dihydrofuranone ring; R 1 and R 2 are each H, thienyl, furanyl, phenyl, etc.; R 3 -R 5 are each H, a halogen, CF 3 NO 2 an alkyl, an alkyl or alkylene bridge between R 4 and R 5 or R 3 and the ring N, benzyl, phenyl, etc.; R 6 in the dihydrofuranon series is H or an alkyl) or its salt. n EXAMPLE: 5-[1-(2-Ethylimidazole)methyl]-4,5-dihydro-3,3-diphenyl-2(3H)furanone. n USE: Antagonist of cholinergic receptors useful as anti-neurogenic bladder disorder agent, anticonvulsant, antisecretory agent or mydriatic agent. n PROCESS: For example, diphenylacetic acid is subjected to dilithium salt formation and treated with allyl bromide to give 2,2-diphenyl-4-pentenoic acid. The sodium salt of the product is treated with bromine to form a cyclic furanone, which is then reacted with a substd. imidazole under heating to give the compound of the formula. n COPYRIGHT: (C)1992,JPO
priorityDate 1990-05-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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