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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2426266Generated: November 2, 2026

N-bromobutanimide → HCID 67148260, compound

https://huagongshe.com/reaction/2426266

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 67147764HCID 67147764—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 67148260HCID 67148260—

Reaction Steps

A mixture of methyl 3-(benzoyloxy)-4-oxo-4,6,7,8,9,10-hexahydropyrimido[1,2-a]azepine-2-carboxylate, N-bromo-succinimide (2 eq.) and α,α′-azoisobutyronitrile (0.45 eq.) in carbon tetrachloride was stirred under reflux for 14 hour. The mixture was cooled to room temperature, the succinimide was filtered off and the solvent was removed under reduced pressure. Methyl 3-(benzoyloxy)-10-bromo-4-oxo-4,6,7,8,9,10-hexahydropyrimido[1,2-a]azepine-2-carboxylate was obtained after flash chromatography (eluents petroleum ether/ethyl acetate, 8:2) as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968553B2
Source datasetuspto-grants-2011_06
ORD IDord-3a6e79591a784a7fb1906d8698bb590f
Source noteuspto-grants-2011_06