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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1012270Generated: October 31, 2026

N-bromobutanimide → HCID 23152327, compound

https://huagongshe.com/reaction/1012270

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 23152701HCID 23152701—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 23152327HCID 2315232778%

Reaction Steps

To a solution of ethyl 3-cyclohexyl-1-ethoxycarbonylmethyl-1H-pyrrolo[2,3-b]pyridine-6-carboxylate (463 mg, 1.34 mmol) in carbon tetrachloride (10 ml) was added N-bromosuccinimide (287 mg, 1.61 mmol), and the mixture was heated under reflux for 4 hr. The mixture was allowed to cool to room temperature and the solvent was evaporated under reduced pressure. The residue was purified by silica gel chromatography (hexane:ethyl acetate-5:1) to give ethyl 2-bromo-3-cyclohexyl-1-ethoxycarbonylmethyl-1H-pyrrolo[2,3-b]pyridine-6-carboxylate (457 mg, yield 64%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977331B1
Source datasetuspto-grants-2011_07
ORD IDord-09c5f4eafe33415ca42082ad841df6d4
Source noteuspto-grants-2011_07