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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2219053Generated: November 1, 2026

N-bromobutanimide → HCID 67148260, compound

https://huagongshe.com/reaction/2219053

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 numberUS07414045B2
Source datasetuspto-grants-2008_08
ORD IDord-8e25f124c51d45db97221a8361f9e441
Source noteuspto-grants-2008_08