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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2422683Generated: October 26, 2026

Ammonium Chloride → 3-Amino-5-bromopyridine-2-carboxamide

https://huagongshe.com/reaction/2422683

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant5-Bromo-3-nitropyridine-2-carboxamideHCID 67244466—
CatalystIronHCID 23925—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product3-Amino-5-bromopyridine-2-carboxamideHCID 2107586270%

Reaction Steps

5-Bromo-3-nitropyridine-2-carboxamide (400 mg, 1.63 mmol), ammonium chloride (435 mg, 8.15 mmol) and iron powder (273 mg, 4.89 mmol) were suspended in methanol (6 mL) and water (3 mL), and stirred at 100° C. for 20 hours. After cooled to room temperature, this was filtered through Celite, and the Celite was washed with methanol. The mother liquid was concentrated, and the residue was dissolved in chloroform and washed with water. The organic layer was concentrated under reduced pressure to obtain the intended compound (246 mg, 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960394B2
Source datasetuspto-grants-2011_06
ORD IDord-e5cc439fcd934ff79d355efdd282b6b3
Source noteuspto-grants-2011_06