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filingDate 1981-07-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1988-08-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_54e8e4818d4884103ac26997af547710
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publicationDate 1988-08-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4766210-A
titleOfInvention Antihypertensive lactams
abstract Antihypertensive compounds of the structure ##STR1## wherein: n is an integer from 0 to 2 inclusive, n R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , and R 7 are independently hydrogen, alkyl having from 1 to 6 carbon atoms, alkenyl having from 2 to 6 carbon atoms, alkynyl having from 2 to 6 carbon atoms, cycloalkyl having from 3 to 16 carbon atoms, phenyl, benzyl, tolyl, naphthyl, phenethyl, indanyl, tetrahydronaphthyl, decahydronaphthyl, pyridyl, quinolyl, pyrrolidyl, pyrrolyl, morpholinyl, thiomorpholinyl, furyl, furfuryl, tetrahydrofurfuryl, benzimidazole, thienyl, imidolyl, or tetrahydroindolyl, and where the R 1 to R 7 groups are alkyl, said groups carrying a substituent selected from hydroxy, alkoxy, amino, carboxy, or carbalkoxy, the alkyl group in alkoxy and carbalkoxy having from 1 to 6 carbon atoms, or R 2 taken together with R 3 and the carbons to which they are attached is tetrahydronapthyl or phenyl, and when phenyl R 1 and R 4 are absent, or R 6 and R 7 taken together with the carbon to which R 6 is attached and the nitrogen to which R 7 is attached form a heterocycle selected from pyrrolidyl, thiazolidine, tetrahydro-isoquinoline, thiomorpholine, or 2,2,5,5-tetramethylthiazolidinie, and n Y is ═O, ═S, ═NR 1 , ═NOR 1 or ═N--NH 2 , R 1 being the same as defined above.
priorityDate 1980-04-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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