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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 67339Generated: October 29, 2026

Ammonia → HCID 20515321, compound

https://huagongshe.com/reaction/67339

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantAmmonium ChlorideHCID 25517—
ReactantRo 14-7437HCID 127597—
SolventMethanolHCID 887—
ProductHCID 20515321HCID 20515321—

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 10.0 g of ethyl 5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylate, 200 ml of methanol, 0.5 g of ammonium chloride and 30 g of ammonia (100%) is stirred in an autoclave under nitrogen (40 bar) at a temperature of 120° C. for 12 hours. After cooling and discharging the over-pressure, the mixture is evaporated to dryness. After partition of the residue between methylene chloride and water, the organic phase is dried and evaporated. The residue is recrystallised from ethyl acetate, there being obtained 5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxamide in the form of white crystals of melting point 274°-275° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04346030
Source datasetuspto-grants-1982_08
ORD IDord-51ba4cee14384b82b54a6fbba37da504
Source noteuspto-grants-1982_08