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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877863Generated: November 1, 2026

Acetonitrile → HCID 86649005, compound

https://huagongshe.com/reaction/1877863

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 66994124HCID 66994124—
SolventWaterHCID 962—
ProductHCID 86649005HCID 8664900574%

Reaction Steps

A mixture of tert-butyl 3-[methyl(1-methylethyl)amino]-6,7-dihydropyrazino[2,3-f][1,4]oxazepine-8(9H)-carboxylate (1.0 g), N-bromosuccinimide (608 mg) and acetonitrile (20 mL) was stirred at room temperature for 16 hr. Water was added, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine, dried over sodium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (solvent gradient: 3→30% ethyl acetate/hexane) to give the title compound (915 mg, 74%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314088B2
Source datasetuspto-grants-2012_11
ORD IDord-dbab7022203b41e28814bed3e42f92dd
Source noteuspto-grants-2012_11