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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378110Generated: November 1, 2026

Ethyl Bromide → HCID 22914417, compound

https://huagongshe.com/reaction/1378110

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl BromideHCID 6332—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 22914458HCID 22914458—
SolventDimethylformamideHCID 6228—
ProductHCID 22914417HCID 2291441721.2%

Reaction Steps

3.75 ml (21.8 mmol) of N-ethyldiisopropylamine and 0.94 ml (12.6 mmol) of 1-bromoethane were added to a solution of 1.0 g (3.16 mmol) of 7-(5-aminomethyl-1,2,4-oxadiazol-3-yl)-5-methyl-5,6-dihydro-4H-imidazo[1,5-a]thieno[3,2-f][1,4]diazepin-4-one in 30 ml of dimethylformamide and the mixture was stirred at 70° for 1 hour. The reaction solution was subsequently evaporated, whereupon the residue was partitioned between methylene chloride and 2N sodium carbonate solution. The aqueous phase was washed three times with methylene chloride. The organic phases were dried with magnesium sulfate, filtered and evaporated. The residue obtained was chromatographed (silica gel, methylene chloride/methanol/aqueous ammonia 110:10:1). There were obtained 250 mg (21%) of 7-(5-diethylaminomethyl-1,2,4-oxadiazol-3-yl)-5-methyl-5,6-dihydro-4H-imidazo[1,5-a]thieno[3,2-f][1,4]diazepin-4-one as a colourless foam, Rf=0.56 (silica gel, methylene chloride/methanol/aqueous ammonia 110:10:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665718
Source datasetuspto-grants-1997_09
ORD IDord-9cdf73a18cbb443ea5b00e79dc7ce72c
Source noteuspto-grants-1997_09