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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26048Generated: October 29, 2026

Potassium Hydroxide → 8-Chloro-6-(2-chlorophenyl)-1,2-dihydro-4H-imidazo[1,5-a] [1,4]benzodiazepin-1-thione-3-carboxylic acid

https://huagongshe.com/reaction/26048

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 54335518HCID 54335518—
SolventMethanolHCID 887—
Product8-Chloro-6-(2-chlorophenyl)-1,2-dihydro-4H-imidazo[1,5-a] [1,4]benzodiazepin-1-thione-3-carboxylic acidHCID 20394585—

Reaction Steps

A solution of 1.1 g (0.02 mole) of potassium hydroxide in 40 ml of methanol was treated with 2.1 g (0.005 mole) of 8-chloro-6-(2-chlorophenyl)-1,2-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepin-1-thione-3-carboxylic acid methyl ester in a beaker. The solution was boiled in a steambath for 15 min and then evaporated at reduced pressure at 50°-60°. An aqueous solution of the residue was acidified with cold 6N aqueous hydrochloric acid adding ice to keep the mixture cold. The solid was collected by filtration, washed with water and air dried on the funnel overnight to yield crude end product. Recrystallization from ethanol gave light tan crystals with mp 277°-280° (dec).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04147875
Source datasetuspto-grants-1979_04
ORD IDord-1092a4007c4c4eb49cab5fbe2165453d
Source noteuspto-grants-1979_04