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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1447331Erstellt: 24. Oktober 2026

Flumazenil → Flumazenil Impurity 8

https://huagongshe.com/de/reaction/1447331

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFlumazenilHCID 3373—
EduktPotassium CyanideHCID 9032—
LösungsmittelMethanolHCID 887—
ProduktFlumazenil Impurity 8HCID 20515347—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04316839
Quelldatensatzuspto-grants-1982_02
ORD IDord-dd1596a79bb74556b6b687e338613445
Quellennotizuspto-grants-1982_02