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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26053Generated: October 30, 2026

Ammonia → 8-Chloro-6-(2-chlorophenyl)-1-methylthio-4H-imidazo[1,5-a] [1,4]benzodiazepine-3-carboxamide

https://huagongshe.com/reaction/26053

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantPotassium BromideHCID 253877—
Reactant8-chloro-6-(2-chlorophenyl)-1-methylthio-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylic acid methyl esterHCID 53743422—
SolventMethanolHCID 887—
Product8-Chloro-6-(2-chlorophenyl)-1-methylthio-4H-imidazo[1,5-a] [1,4]benzodiazepine-3-carboxamideHCID 20394582—

Reaction Steps

A mixture of 3 g (0.007 mole) of 8-chloro-6-(2-chlorophenyl)-1-methylthio-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylic acid methyl ester and 60 ml of 25% solution of ammonia in methanol was heated at 130° in a steel bomb for 18 hrs. The contents of the bomb were evaporated at reduced pressure to give light tan crystals, which were recrystallized from methanol/methylene chloride to yield light tan prisms with mp 270°-274° (dec.). Uv λ max 217 mμ (ε=47,200) infl 242 (23,200) sh 270 (11,500), ir (KBr) 3365, 3250, 3215, 3150 cm-1 (NH2) 1675, 1650, 1590 (CON).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04147875
Source datasetuspto-grants-1979_04
ORD IDord-e62f6bd06dca4c37ae3106c593afc6b0
Source noteuspto-grants-1979_04