摘要:
Novel 2(2-(1,3-diazacycloalk-2-enyl))benzophenone compounds and novel 1,3-diazacycloalkenyl(2,1-a)isoindole compounds having useful analgesic and psychostimulant properties are prepared inter alia by condensation of o-benzoylbenzaldehydes with aliphatic diamines.
摘要:
Compounds of the class of 2,3,4,5-tetrahydro-1H-1,4diazepino(1,2a)indoles useful for their pharmacological properties and novel intermediates used in the syntheses thereof. The 2,3,4,5-tetrahydro-1H-1,4-diazepino (1,2a) indoles are useful agents for lowering blood pressure.
WHEREIN R1 IS A LOWER ALKYL GROUP OF FROM 1 TO 2 CARBON ATOMS; R2 IS A MEMBER SELECTED FROM THE GROUP CONSISTING OF A HYDROGEN ATOM AND A METHYL GROUP; AND HAL REPRESENTS A HALOGEN ATOM; AND THE PHARMACEUTICALLY ACCEPTABLE ACID ADDITION SALTS THEREOF.
摘要:
A HYDRAZINE IS REACTED WITH A O-CARBONYL ACID TO PROVIDE 2,3,5,6-TETRAHYDRO-4H-1,2-DIAZEPINE-3-ONES OF THE FORMULA
2-R,3-(O=),4-R1,5-R2,6-R3,7-AR-2,3,5,6-TETRAHYDRO
4H-1,2-DIAZEPINE
WHEREIN AR IS PHENYL, TOLYL, HALOPHENYL, METHOXYPHENYL, NAPHTHYL, OR THIENYL, R IS HYDROGEN, LOWER ALKYL, CARBOXYL (LOWER ALKYL), DI(LOWER ALKYL) AMINO (LOWER ALKYL), MORPHOLINO(LOWER ALKYL) OR PYRROLIDINO(LOWER ALKYL), AND EACH OF R1, R2 AND R3 IS INDEPENDENTLY HYDROGEN, LOWER ALKYL, OR A PHENYL GROUP, AND THE PHARMACEUTICALLY ACCEPTABLE SALTS AND QUANTERNARY AMMONIUM DERIVATIVES THEREOF. THE COMPOUNDS ARE USEFUL IN PHAROACEUTICAL CHEMISTRY, HAVING BEEN FOUND PARTICULARYL USEFUL AS PSYCHOTROPIC AGENTS.
摘要:
CERTAIN 2-TRIMETHOXYBENZOYLIMINO-1,3-DIAZACYCLOALKENES AND -ALKADIENES, USEFUL AS INTERMEDIATES, ALSO EXHIBIT CENTRAL NERVOUS SYSTEM DEPRESSING EFFECTS.
WHEREIN R, R'' AND R" ARE LOWER ALKYL AND N IS 2 OR 3, WHICH ARE USEFUL AS ANTIDEPRESSANT HAVING LOW TOXICITY, PREPARED BY THE REACTION OF THE CORRESPONDING 10-UNSUBSTITUTED-DIBENZODIAZEPIN-11(10)-ONE COMPOUNDS WITH AN W-DIALKYLAMINOALKYL HALIDE.
摘要:
AND SALTS THEREOF; WHERE R1 IS HYDROGEN OR METHYL, AND AR IS PHENYL, O-FLUOROPHENYL, O-CHLOROPHENYL, OR 2-TRIENYL; AND THEIR PRODUCTION BY (A) REACTING A 3-AROYL-2-(2-HALOACETAMIDO)TETRAHYDROBENZOTHIOPHENE OR A SALT THEREOF WITH AMMONIA, (B) REACTING A 3-AROYL-2-(2-PHTHALIMIDOACETAMIDO)TETRAHYDROBENZOTHIOPHENE WITH ANHYDROUS HYDRAZINE, (C) REACTING A 2-(2-AMINOACETAMIDO)-3-AROYLTETRAHYDROBENZOTHIOPHENE SALT WITH A BASE, AND (D) REACTING ONE OF THE TETRAHYDROBENZOTHIENODIAZEPINONE COMPOUNDS WHEREIN R1 IS HYDROGEN WITH A METHHLATING AGENT IN THE PRESENCE OF A BASE. THE COMPOUNDS OF THE INVENTION ARE USEFUL AS ANTICONVULSANT AND ANTI-ANXIETY AGENTS.
WHEREIN THE R SUBSTITUENTS ARE THE SAME OR DIFFERENT AND ARE SELECTED FROM THE GROUP CONSISTING OF HYDROGEN ATOMS AND ALKYL GROUPS CONTAINING 1 TO 18 CARBON ATOMS ARE PREPARED BY REACTING AN ETHYLENE-DIAMINE WITH AN ALIPHATIC ALPHA-BETA UNSATURATED ALDEHYDE OR KETON AND THEN CATALYTICALLY HYDROGENATING THE REACTION MIXTURE. NOVEL ALKYL SUBSTITUTED HEXAHYDRO-1,4-DIAZEPINES ARE DISCLOSED.