摘要:
THE INVENTION CONCERNS NOVEL COMPOUNDS OF FORMULA:
2-R2,4-(R1-NH-CH2-CH(-OH)-CH2-O-)INDOLE
IN WHICH R1 IS LOWER ALKYL, CYCLOALKYL HAVING 3 TO 4 CARBON ATOMS, PHENYLALKYL OF 8 TO 10 CARBON ATOMS OR 1-ADAMANTYL, AND R2 IS HYDROXYMETHYL OR COOR5, WHERE R5 IS A HYDROGEN ATOM OR LOWER ALKYL RADICAL, WHICH ARE USEFUL AS B-ADRENERGIC BLOCKING AGENTS. PROCESSES FOR THE PRODUCTION OF THE COMPOUNDS OF THE INVENTION AND INTERMEDIATES FOR THE USE THEREIN ARE DESCRIBED.
摘要:
WHEREIN X is hydrogen, halogen, methyl or methylthio and Y is hydrogen, OR X is hydrogen and Y is methyl, OR BOTH X and Y are chlorine. The compounds and pharmaceutically acceptable acid addition salts thereof are vasoconstrictors.
The present invention concerns compounds of the formula:
摘要:
The present invention provides fluorene derivatives of formula,
IN WHICH R is isopropyl, secondary butyl, tertiary butyl, 3phenylpropyl, 1-cyano-2-propyl,tert. pentyl or 3-pentyl, and either X is hydrogen and Y is hydroxy, or X and Y together are oxo, and pharmaceutically acceptable acid addition salts thereof. The compounds of the invention exhibit Beta -blocking activity.
WHEREIN A AND B TOGETHER FORM A SINGLE BOND, OR A IS ETHOXY OR HYDROXYMETHYL AND B IS HYDROGEN, R1 IS HYDROGEN OR HYDROXY, R2 IS HYDROGEN OR METHYL, R3 IS METHYL, OR R3 IS HYDROGEN WHEN R2 IS METHYL, AND R4 IS HYDROGEN, METHOXY OR CHLORINE. THE COMPOUNDS ARE USEFUL IN THE PROPHYLAXIS OF THROMBOSIS AND EMBOLISM AND FOR IMPROVING MICROCIRCULATION.
6H-INDOLO(4,3-FG)QUINOLINE WHERE THE 10,10A POSITION IS
X--Y
IN WHICH R1 IS HYDROGEN OR METHYL, AND R2 IS ARALKYL OF 7 TO 9 CARBON ATOMS, ARYL OR ARYL SUBSTITUTED BY ONE OR MORE OF THE FOLLOWING RADICALS: METHYL, ALKOXY OF 1 TO 4 CARBON ATOMS, CHLORINE OR BROMINE, AND
X--Y IS -CH=C AND THEIR ACID ADDITION SALTS. THE COMPOUNDS IN WHICH R1 IS HYDROGEN AND
X--Y IS -CH=C HAVE ANTIDEPRESSIVE PROPERTIES. THE REMAINING COMPOUNDS HAVE SEDATIVE PROPERTIES. THE PREPARATION OF THE COMPOUNDS IS ALSO DESCRIBED.
摘要:
COMPOUNDS ARE OF THE CLASS OF 2,5(5) - DI(TRI)SUBSTITUTED - 10B - HYDROXY - 3,6 - DIOXO-OCTAHYDRO-OXAZOLO (3,2-A)PYRROLO(2,1-C)PYRAZINE DERIVATIVES OF LYSERGIC ACID AND ARE USEFUL AS VASOTONIC AGENTS. THE COMPOUNLS ARE PREPARED BY REACTING AN APPROPRIATE AMINOCYCLOL WITH LYSERGIC ACID.
WHEREIN R1 IS LOWER ALKYL, CYCLOALKYL OF 3 OR 4 CARBON ATOMS OR PHENYALKYL OF AT LEAST 8 CARBON ATOMS, THE PHENYL NUCLEUS THEREOF BEING SEPARATED FROM THE NITROGEN ATOM BY AT LEAST TWO ALKYL CARBON ATOMS, R2 IS HYDROGEN OR METHYL, AND EACH OF R3 AND R4 IS HYDROGEN OR LOWER ALKYL, OR R3 IS AMINO, LOWER ALKYLAMINO, CYCLOALKYL OF 3 OR 4 CARBON ATOMS OR PHENYL, AND R4 IS HYDROGEN, OR R3 AND R4 TOGETHER WITH THE NITROGEN ATOMS TO WHICH THEY ARE BOUND, ARE 1-PYRROLIDINYL, 1-PIPERIDINYL OR 1-MORPHOLINYL, AND ACID ADDITION SALTS THEREOF. THE COMPOUNDS AND THEIR PHARMACEUTICALLY ACCEPTABLE ACID ADDITION SALTS HAVING A BLOCKING EFFECT ON THE ADRENEGIC B-RECEPTORS.
摘要:
The invention concerns new indol derivatives of the formula:
WHEREIN R1 is lower alkyl, cycloalkyl of three or four carbon atoms, or 3-phenylpropyl, as well as processes for the production thereof. The compounds have a blcoking effect on the vascular adrenergic Beta -receptors.