Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2198696Generated: October 30, 2026

Flumazenil → Flumazenil Impurity 8

https://huagongshe.com/reaction/2198696

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 numberUS04359420
Source datasetuspto-grants-1982_11
ORD IDord-9692dce089904a06a0801f72e15214ac
Source noteuspto-grants-1982_11