Process for preparing halo triazolo benzodiazepine

Chemistry of carbon compounds – Miscellaneous organic carbon compounds – C-metal

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C07D48704

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active

039910709

ABSTRACT:
Preparing 1-halo-6-phenyl-4H-s-triazolo[4,3-a][1,4]benzodiazepines by reacting an N-halosuccinimide with a 2-[3-(phthalimidomethyl)triazolyl]benzophenone to form the 2-[5-halo-3-(phthalimidomethyl)triazolyl] benzophenone and reacting the 2-[5-halo-3-(phthalimidomethyl)triazol-4-yl]benzophenone with hydrazine or a primary amine in an organic liquid solvent medium at 25.degree. to 100.degree. C. The products of the process have CNS tranquilizer and sedative properties but are also of interest for use as intermediates to prepare 2,4-dihydro-6-phenyl-1H-s-triazolo[4,3-a] [1,4]benzodiazepin-1-ones which are of clinical interest for their CNS tranquilizer, sedative and anti-depressant drug use properties in mammalian animals including humans.

REFERENCES:
patent: 3709899 (1973-01-01), Hester
patent: 3842090 (1974-10-01), Gall et al.
patent: 3880878 (1975-04-01), Hester
patent: 3882139 (1975-05-01), Gall et al.
patent: 3891666 (1975-06-01), Hester

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