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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154474Generated: October 30, 2026

Potassium Cyanide → HCID 54376131, compound

https://huagongshe.com/reaction/1154474

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CyanideHCID 9032—
Reactant3-Chlorobenzyl alcoholHCID 70117—
Reactantethyl (S)-8-chloro-11,12,13,13a-tetrahydro-9-oxo-9H-imidazo[1,5-a]pyrrolo[2,1-c][1,4]-benzodiazepine-1-carboxylateHCID 53890667—
SolventDichloromethaneHCID 6344—
ProductHCID 54376131HCID 54376131—

Reaction Steps

A mixture of 3.45 g (10 mmol) of ethyl (S)-8-chloro-11,12,13,13a-tetrahydro-9-oxo-9H-imidazo[1,5-a]pyrrolo[2,1-c][1,4]benzodiazepine-1-carboxylate, 100 mg of powdered potassium cyanide and 14.2 g of 3-chlorobenzyl alcohol is stirred at 130° for 48 hours, the mixture is diluted with about 20 ml of methylene chloride and chromatographed on about 300 g of silica gel while eluting with ethyl acetate. By crystallization from ethyl acetate and hexane there is obtained m-chlorobenzyl (S)-8-chloro-11,12,13,13a-tetrahydro-9-oxo-9H-imidazo[1,5-a]pyrrolo[2,1-c][1,4]benzodiazepine-1-carboxylate of melting point 114°-116°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04489003
Source datasetuspto-grants-1984_12
ORD IDord-e9ed4e6709994905931f55670745c17d
Source noteuspto-grants-1984_12