Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 430661Generated: October 25, 2026

Water → 8-Methoxy-3-methyl-6-phenyl-11H-imidazo[1,2-c][2,3]benzodiazepine

https://huagongshe.com/reaction/430661

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant(2-Methyl-1,3-dioxolan-2-yl)methanamineHCID 12434663—
Reactant8-methoxy-1-phenyl-4,5-dihydro-3H-2,3-benzodiazepine-4-thioneHCID 17887821—
Solvent2-MethoxyethanolHCID 8019—
Product8-Methoxy-3-methyl-6-phenyl-11H-imidazo[1,2-c][2,3]benzodiazepineHCID 18183158—

Reaction Steps

500 mg of 8-methoxy-1-(phenyl)-4,5-dihydro-3H-2,3-benzodiazepine-4-thione is stirred in 1.5 ml of ethylene glycol monomethyl ether (Cellosolve®) and 548 mg of 2-aminomethyl-2-methyl-1,3-dioxolane while argon is passing through it for 10 hours at 60° C. After filtration and washing with cold ethanol and diisopropyl ether, 550 mg of imino compound, which is dissolved in 10 ml of ethanol, mixed with 10 ml of concentrated hydrochloric acid and refluxed for 3 hours, is obtained. It is added to water, set at pH 11 and extracted with ethyl acetate. The ethyl acetate phase is washed with water, dried, filtered and concentrated by evaporation. After recrystallization from ethyl acetate/diisopropyl ether, 240 mg of 8-methoxy-3-methyl-6-phenyl-11H-imidazo[1,2-c][2,3]benzodiazepine with a melting point of 140° C. is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06323197B1
Source datasetuspto-grants-2001_11
ORD IDord-50f2e2a4e9f640f3a950021f1c6e68e2
Source noteuspto-grants-2001_11