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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 67320Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/67320

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CyanideHCID 9032—
EduktRo 14-7437HCID 127597—
LösungsmittelMethanolHCID 887—
Produktmethyl 5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylateHCID 10378479—

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 66 mg of potassium cyanide are heated to boiling under reflux for 24 hours in 10 ml of methanol. 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 methyl 5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylate of melting point 212°-214° 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-2343817238154b91a71b7b1a643bedcf
Quellennotizuspto-grants-1982_08