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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378040Generated: November 1, 2026

Dichloromethane → HCID 86751231, compound

https://huagongshe.com/reaction/1378040

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantPropargyl bromideHCID 7842—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 22914303HCID 22914303—
ProductHCID 86751231HCID 8675123145%

Reaction Steps

328 mg (1.0 mmol) of 3-(3-aminomethyl-1,2,4-oxadiazol-5-yl)-8-fluoro-5,6-dihydro-5-methyl-4H-imidazo[1,5-a][1,4]benzodiazepin-6-one in 6 ml of methylene chloride were treated under argon with 1.2 ml (7.0 mmol) of N-ethyldiisopropylamine and 0.65 ml (6.0 mmol) of propargyl bromide (80% in toluene) and the mixture was stirred at room temperature under argon for 19 hrs. The solution was washed with 10 ml of water and evaporated, and the crude product was purified by chromatography on 15 g of silica gel (methylene chloride/acetone 9:1). The eluate was evaporated and the residue was taken up in 5 ml of methanol. The solution was acidified with 5 ml of ethereal hydrochloric acid and the white crystals were filtered off. There were obtained 200 mg (45%) of 3-[3-[bis-(prop-2-ynyl)-aminomethyl]-1,2,4-oxadiazol-5-yl]-8-fluoro-5-methyl-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepin-6-one hydrochloride (4:5) of m.p. 186°-189° (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665718
Source datasetuspto-grants-1997_09
ORD IDord-524dabdd553d4f27b02680ef652a9fc6
Source noteuspto-grants-1997_09