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filingDate 1979-10-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a744850d4d91b1d9453871448ea9a546
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2664323b169efa1c73a9e577c279f9c8
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publicationDate 1980-05-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0011373-A1
titleOfInvention 5-Oxo-5H-hexahydrofuro(3,2-b)pyrrole derivatives, their preparation, intermediates, and pharmaceutical compositions containing said derivatives
abstract The novel 5-oxo-5H-hexahydrofuro [3,2-b] pyrrole derivatives of formula (I):n wherein:n A is CH-and n is 1 to 6; or A is C=CH- and n is 0 to 5; or A is CH-CH=CH- and n is 0 to 4; and R 1 is hydrogen or C 1-6 alkyl; R 2 is hydrogen or C 1-6 alkyl; and R 3 is C 4-9 alkyl, C 5-7 cycloalkyl or C 5-7 cycloalkyl-C 1-6 alkyl; e.g. 2-(4'-ethoxycarbonyl-n-butyl)-4-(3' '-hydroxy-3' '-methyl-n-nonyl)- 5-oxo-5H-hexahydrofuro [3,2-b] pyrrole, and salts thereof, have antiplatelet aggregation and bronchodilation activity. They can be prepared by (I) demercuration, (II) dehydrohalogenation or (III) oxidation of a compound of formula (VI):n wherein R R 2 and R 3 are as defined above, p is 0 to 5 and X is (I) a mecuri salt, (II) halo or (III) phenyl selenyl respectively. The preparation of the compounds of formula (VI) is described.
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