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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 67342Generated: October 25, 2026

Flumazenil → Flumazenil Impurity 8

https://huagongshe.com/reaction/67342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFlumazenilHCID 3373—
ReactantPotassium CyanideHCID 9032—
SolventMethanolHCID 887—
ProductFlumazenil Impurity 8HCID 20515347—

Reaction Steps

A mixture of 3.5 g (11.5 mmol) of ethyl 8-fluoro-5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylate, 0.15 g of potassium cyanide and 40 ml of methanol is stirred at the boiling point for 2.5 hours. The solvent is distilled off on a rotary evaporator and the residue is taken up in chloroform. After filtration from insoluble material, the filtrate is concentrated. After recrystallisation of the residue from ethyl acetate, there is obtained methyl 8-fluoro-5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylate of melting point 195°-196.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04346031
Source datasetuspto-grants-1982_08
ORD IDord-eefa9fc5fb1a40a28a98a7cdb2980247
Source noteuspto-grants-1982_08