Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223194Generated: October 31, 2026

Water → t-butyl 5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylate

https://huagongshe.com/reaction/223194

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactanttert-ButanolHCID 6386—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant5-methyl-6-oxo-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylic acidHCID 10332676—
SolventPyridineHCID 1049—
Productt-butyl 5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylateHCID 398203—

Reaction Steps

A suspension of 2.6 g (10 mmol) of 5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylic acid in 20 ml of pyridine is firstly treated with 25 ml of t-butanol and subsequently treated dropwise at -5° with 1.1 ml of phosphorus oxychloride. The mixture is stirred at -5° for 15 minutes and at room temperature for 48 hours, poured into 250 ml of water and extracted four times with chloroform. The chloroform extracts are washed three times with dilute sodium hydroxide and three times with water, dried over magnesium sulphate and evaporated. After recrystallization of the residue from ethyl acetate, there is obtained t-butyl 5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylate of melting point 216°-217°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04352817
Source datasetuspto-grants-1982_10
ORD IDord-2f74af6265f048dfabc3320eefd0a0c7
Source noteuspto-grants-1982_10