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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223183Generated: October 29, 2026

Ammonia → Ethyl 5-methyl-8-nitro-6-oxo-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylate

https://huagongshe.com/reaction/223183

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantNitric AcidHCID 944—
ReactantRo 14-7437HCID 127597—
SolventSulfuric AcidHCID 1118—
ProductEthyl 5-methyl-8-nitro-6-oxo-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylateHCID 15480886—

Reaction Steps

2.85 g of ethyl 5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylate are dissolved in a mixture of 10 ml of 98 percent nitric acid and 15 ml of 98 percent sulphuric acid and heated to 120° for 2 hours. Subsequently, the mixture obtained is cooled to room temperature, poured onto ice, neutralized with about 25 percent ammonia and extracted with chloroform. The chloroform extracts are dried over magnesium sulphate and evaporated. After recrystallization of the residue from ethyl acetate, there is obtained ethyl 5,6-dihydro-5-methyl-8-nitro-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylate of melting point 197°-198°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04352815
Source datasetuspto-grants-1982_10
ORD IDord-968c1a452e6640f3abb1acc48271b301
Source noteuspto-grants-1982_10