Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217211Generated: October 29, 2026

6-nitropyridin-2-amine → HCID 56923659, compound

https://huagongshe.com/reaction/217211

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-nitropyridin-2-amineHCID 2762881—
ReactantN-BromosuccinamideHCID 9834204—
SolventAcetonitrileHCID 6342—
ProductHCID 56923659HCID 56923659153.3%

Reaction Steps

To a stirred solution of 6-nitro-pyridin-2-ylamine (1.0 g, 7.18 mmol) in CH3CN (100 mL), protected from light and under nitrogen atmosphere, N-bromosuccinamide (636 mg, 3.59 mmol) was added at 0° C. After 1 hour, another portion of N-bromosuccinamide (636 mg, 3.59 mmol) was added. The reaction mixture was allowed to warm to room temperature and stirring was continued overnight. The reaction mixture was then quenched by the addition of saturated aqueous Na2S2O3 and extracted with ethyl acetate (3×30 mL). The combined organic extracts were washed with water, brine, dried over MgSO4 (anhydrous) and concentrated in vacuo. The crude product was purified by Biotage using 10% ethyl acetate in hexane to afford 1.2 g of 5-bromo-6-nitro-pyridin-2-ylamine (10).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193363B2
Source datasetuspto-grants-2012_06
ORD IDord-10b20d1264f743f08f34014207046a02
Source noteuspto-grants-2012_06