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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 67321Erstellt: 25. Oktober 2026

Potassium Cyanide → isopropyl 5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine 3-carboxylate

https://huagongshe.com/reaction/67321

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CyanideHCID 9032—
EduktRo 14-7437HCID 127597—
LösungsmittelIsopropanolHCID 3776—
Produktisopropyl 5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine 3-carboxylateHCID 19735056—

Reaktionsschritte

285 mg (1 mmol) of ethyl 5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylate and 50 mg of potassium cyanide are stirred at 60° C. for 72 hours in 10 ml of 2-propanol. Then, the mixture is concentrated on a rotary evaporator, the residue is partitioned between water and chloroform, extracted twice with chloroform, the chloroform phase is dried over magnesium sulphate and evaporated. There is obtained isopropyl 5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine 3-carboxylate of melting point 190°-192° C. This product is uniform according to thin-layer chromatography.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04346030
Quelldatensatzuspto-grants-1982_08
ORD IDord-5900985991ac45158a44abf67892676c
Quellennotizuspto-grants-1982_08