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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378103Generated: November 1, 2026

2-Butene, 1-bromo-3-methyl- → HCID 131720188, compound

https://huagongshe.com/reaction/1378103

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Butene, 1-bromo-3-methyl-HCID 70092—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 53986672HCID 53986672—
SolventDichloromethaneHCID 6344—
ProductHCID 131720188HCID 131720188—

Reaction Steps

1.5 ml (8.6 mmol) of N-ethyldiisopropylamine and 0.28 ml (2.4 mmol) of dimethylallyl bromide were added to a solution of 453 mg (1.2 mmol) of (S)-1-(3-aminomethyl-1,2,4-oxadiazol-5-yl)-11,11a-dihydro-8H, 10H-azeto[1,2-a]imidazo[5,1-c]thieno[3,2-e][1,4]diazepin-8-one in 20 ml of methylene chloride and the mixture was stirred at room temperature for 20 hours. The reaction solution was subsequently diluted with methylene chloride and washed three times with water. The organic phases were dried with magnesium sulfate, filtered and evaporated. The is residue obtained was chromatographed (silica gel, methylene chloride/methanol/aqueous ammonia 140:10:1). There were obtained 240 mg (43%) of (S)-1-[3-bis-[3-methyl-but-2-enyl)-aminomethyl]-1,2,4-oxadiazol-5-yl]-11,11a-dihydro-8H,10H-azeto[1,2-a]imidazo[5,1-c]thieno[3,2-e][1,4]diazepin-8-one as a colourless foam, Rf=0.55 (silica gel, methylene chloride/methanol/aqueous ammonia 140:10:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665718
Source datasetuspto-grants-1997_09
ORD IDord-c907df6075d946e49c82ae3561809fe4
Source noteuspto-grants-1997_09