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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603629Generated: November 1, 2026

6-Bromo-4-nitropyridine-2-carboxamide → 6-Bromo-4-(4-nitrophenylsulphanyl)-pyridine-2-carboxamide

https://huagongshe.com/reaction/1603629

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Bromo-4-nitropyridine-2-carboxamideHCID 19605533—
Reactant4Nitrothiophenol potassium saltHCID 70002681—
SolventDimethylformamideHCID 6228—
Product6-Bromo-4-(4-nitrophenylsulphanyl)-pyridine-2-carboxamideHCID 1960549487.5%

Reaction Steps

0.25 g (0.001 mol) of 6-bromo-4-nitropyridine-2-carboxamide was dissolved in 5 ml of dimethylformamide, treated with 0.19 g (0.001 mol) of 4-nitrothiophenol potassium salt and stirred at room temperature for 18 hrs. The reaction mixture was partitioned in water and ethyl acetate and the organic phase was washed with water and sat. sodium chloride solution, dried over MgSO4 and concentrated in a vaccum. The residue was chromatographed on silica gel with ethyl acetate/hexane 1:1. There was obtained 0.31 g (86%) of 6-bromo-4-(4-nitrophenylsulphanyl)-pyridine-2-carboxamide as yellowish crystals; m.p.: 192-194° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05990105
Source datasetuspto-grants-1999_11
ORD IDord-76fa1f9c95374dc0bcaa645581d33804
Source noteuspto-grants-1999_11