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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1606959Generated: November 3, 2026

Dimethylformamide → 3-ethynyl-8-fluoro-4,5-dihydro-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-one

https://huagongshe.com/reaction/1606959

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant3-[(Z)-2-chlorovinyl]-8-fluoro-4,5-dihydro-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-oneHCID 86743358—
SolventWaterHCID 962—
Product3-ethynyl-8-fluoro-4,5-dihydro-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-oneHCID 19851546—

Reaction Steps

3.70 g (12.7 mmol) of 3-[(Z)-2-chlorovinyl]-8-fluoro-4,5-dihydro-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-one was heated to boiling under reflux for 4 hours together with 2.26 ml (15.2 mmol) of 1,8-diazabicyclo[5.4.0]undec-7-ene 30 ml of N,N-dimethylformamide. The reaction mixture was subsequently poured into 400 ml of water and extracted five times with methylene chloride. The organic extracts were washed four times with water, dried over magnesium sulphate and evaporated. The residue was dissolved in ethyl acetate, treated with charcoal and recrystallized from ethyl acetate. There was obtained 3-ethynyl-8-fluoro-4,5-dihydro-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepine-6-one of melting point 207°-208°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04863920
Source datasetuspto-grants-1989_09
ORD IDord-cb31e1cdbafa47bab0b2d74ccb3dcb1a
Source noteuspto-grants-1989_09