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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615867Generated: October 31, 2026

N-bromobutanimide → HCID 66552358, compound

https://huagongshe.com/reaction/1615867

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantBenzoic acid, 3-(5-amino-2-pyridinyl)-, ethyl esterHCID 66552355—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 66552358HCID 6655235886.2%

Reaction Steps

To a solution of ethyl 3-(5-aminopyridin-2-yl)benzoate (7.52 g, 31.06 mmol) in DMF (150 mL) was added N-bromosuccinimide (5.58 g, 31.37 mmol) at 0° C. for 5 min. The reaction mixture was quenched with satd. NaHCO3 solution (150 mL) at 0° C. The mixture was partitioned between ethyl acetate and water. The organic layer was separated and the aqueous layer was extracted with ethyl acetate. The combined organic extracts were washed with brine, dried over MgSO4, filtered and concentrated. The crude product was purified by flash column chromatography using a 85:15 v/v hexane:ethyl acetate as solvent to afford ethyl 3-(5-amino-6-bromopyridin-2-yl)benzoate (8.6 g, 86% yield) as a reddish brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765747B2
Source datasetuspto-grants-2014_07
ORD IDord-0ad1f10dee9e48018d79330c529ba856
Source noteuspto-grants-2014_07