Abstract:
4-Aryl-2,3,3a,4,5,6,7,8,9,9b-decahydro-1H-pyrrolo-(3,4f)quinolines, 4-aryl-2,3,3a,4,5,7,8,9,9a,9b-decahydro-1-Hpyrrolo(3,4-f)quinolinium salts, intermediates for their preparation and methods for their preparation are disclosed. In addition, pharmaceutical compositions containing said compounds and methods for using said compositions as antiflammatory, antianginal and anti-arrhythmic agents and to reduce blood pressure are reported.
Abstract:
The new 7-amino-decahydro-quinolines are manufactured by hydroxygenating 5-amino-2-( Beta -cyanoethyl)-5-cyclohexen-1-one in a manner which is in itself known. The 5-amino-2-( Beta cyanoethyl)-5-cyclohexen-1-ones used as the starting substances can be obtained by several reactions, which are disclosed by several publications. One reaction is the cyclisation of cyanoethylated aliphatic ketones in the presence of suitable catalysts. The new 7-amino-decahydro-quinolines represent valuable curing agents for epoxide resins and advantageously 0,5 to 1,3 equivalents of nitrogen-bonded active hydrogen atoms of the 7-amino-decahydro-quinolines are used per 1 equivalent of epoxide groups of the polyepoxide compound.
Abstract:
WHEREIN A is O or S and X, Y, R1, R2, n, n'' and n'''' are as defined hereinafter. These compounds are useful as antiinflammatory agents, and central nervous system stimulants or depressants depending on dosage.
3-(Aminoalkoxy)-2,3-dihydroquinobenzoxa(or thia) zepine derivatives are provided having the structures
Abstract:
A SERIES OF NITROSOAMINES WHICH COMPRISE 4-N-NITROSON-ALKYLAMINOBENZYLIDENE DERIVATIVES OF A FUSED BICYCLIC MOIETY SELECTED FROM 1-INDENE, 2-METHYL QUINOLINE, 4-METHYL QUINOLINE, AND 1-METHYL ISOQUINOLINE. IN CONTRAST TO THE CARCINOGENIC ACTIVITY EXEMPLIFIED BY RELATED NITROSO AND AMINO COMPOUNDS, MEMBERS OF THE PRESENT GROUP OF NITROSO COMPOUNDS HAVE EXHIBITED CARCINOSTATIC ACTIVITY IN ANIMALS IN STANDARD TESTS AGAINST WALKER 256 TUMOR.
Abstract:
1-CYCLOPRPOYLMETHYLENEAMINO-3,4- DIHYDROISQUINOLINE IS A NOVEL COMPOUND POSSESSING HYPOTENSIVE ACTIVITY. IT MAY BE PREPARED BY THE REACTION OF CYCLOPROPYLMETHYLENE AMINO WITH 1,2,3,4-TETRAHYDRO-1-ISOQUINOLTHIONE OR WITH 1-ALKYLTHIO-3,4-DIHYDROISOQUINOLINE.
Abstract:
Trichloro ethylidine amine derivatives of quinolines, thiazoles and tetrahydronaphthalenes having anthelmonthic and fungicidal activity are disclosed.