Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154455Generated: November 3, 2026

Potassium Cyanide → benzyl (S)-8-chloro-11,12,13,13a-tetrahydro-9-oxo-9H-imidazo[1,5-a]pyrrolo[2,1-c][1,4]benzodiazepine-1-carboxylate

https://huagongshe.com/reaction/1154455

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—
SolventBenzyl AlcoholHCID 244—
Productbenzyl (S)-8-chloro-11,12,13,13a-tetrahydro-9-oxo-9H-imidazo[1,5-a]pyrrolo[2,1-c][1,4]benzodiazepine-1-carboxylateHCID 54076798—

Reaction Steps

5 g (14.5 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, 70 mg of powdered potassium cyanide and 20 ml of benzyl alcohol are stirred at 110° for 1 hour, evaporated to dryness and the residue is taken up in chloroform. The solution is washed with water, dried over magnesium sulphate and evaporated. By recrystallization from ethanol and ether there is obtained benzyl (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 141°-142°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04489003
Source datasetuspto-grants-1984_12
ORD IDord-37346b1705224259ae919e92bc89035e
Source noteuspto-grants-1984_12