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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154476Generated: October 29, 2026

Potassium Cyanide → HCID 54320306, compound

https://huagongshe.com/reaction/1154476

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CyanideHCID 9032—
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—
Solvent2-Methoxybenzyl alcoholHCID 69154—
ProductHCID 54320306HCID 54320306—

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 (1.5 mmol) of potassium cyanide and 20 ml of 2-methoxybenzyl alcohol is stirred at 110° for 36 hours, the resulting ethanol being removed in vacuo from time to time. The solvent is subsequently removed by distillation in a high vacuum and the residue is chromatographed on silica gel while eluting with ethyl acetate. By recrystallization from ethyl acetate/n-hexane there is obtained o-methoxybenzyl (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 178°-179°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04489003
Source datasetuspto-grants-1984_12
ORD IDord-6c2a438661904f239dffb10ba24ef6c5
Source noteuspto-grants-1984_12