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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378045Generated: October 30, 2026

Allyl bromide → HCID 22914325, compound

https://huagongshe.com/reaction/1378045

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 22914503HCID 22914503—
SolventDimethylformamideHCID 6228—
ProductHCID 22914325HCID 2291432582.4%

Reaction Steps

1.5 g (4.4 mmol) of 3-(5-aminomethyl-1,2,4-oxadiazol-3-yl)-7-chloro-5,6-dihydro-5-methyl-4H-imidazo[1,5-a][1,4]benzodiazepin-6-one, 20 ml of N,N-dimethylformamide, 210 ml (12 mmol) of N-ethyldiisopropylamine and 1.16 g (9.6 mmol) of allyl bromide were stirred at room temperature for 4 hours. The reaction solution was evaporated and the residue was chromatographed on 250 g of silica gel while eluting with ethyl acetate. The uniform fractions were evaporated. There were obtained 1.54 g (82%) of 3-(5-diallylaminomethyl-1,2,4-oxadiazol-3-yl)-7-chloro-5,6-dihydro-5-methyl-4H-imidazo[1,5-a][1,4]benzodiazepin-6-one, which was converted into the hydrochloride of m.p. 126°-130°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665718
Source datasetuspto-grants-1997_09
ORD IDord-b7f1d786abb7487f9b0a1102980b54fa
Source noteuspto-grants-1997_09