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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1630887Generated: November 2, 2026

Acetic Acid → N-(5-bromo-pyridin-3-ylmethyl)-methanesulfonamide

https://huagongshe.com/reaction/1630887

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonamideHCID 72879—
ReactantSodium BicarbonateHCID 516892—
Reactant5-Bromo-3-pyridinecarboxaldehydeHCID 2784734—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Solvent1,2-DichloroethaneHCID 11—
ProductN-(5-bromo-pyridin-3-ylmethyl)-methanesulfonamideHCID 59534656—

Reaction Steps

To a solution of 5-bromo-3-pyridine-carboxaldehyde (1.5 g, 7.9 mmol), methanesulfonamide (0.5 g, 5.3 mmol), acetic acid (0.637 g, 10.6 mmol), triethylamine (1.07 g, 10.6 mmol) in DCE (50 mL) at ambient temperature is added NaBH(OAc)3 (3.14 g, 14.84 mmol). The reaction mixture is stirred overnight. Aqueous NaHCO3 (20 mL) is added and the organic phase is separated. The aqueous phase is extracted with dichloromethane and the combined organic phase is dried over Na2SO4. Concentration affords a residue which is purified by silica gel flash chromatography with a methanol in dichloromethane gradient to afford N-(5-bromo-pyridin-3-ylmethyl)-methanesulfonamide as a solid. MS (ESI) m/z 266.9 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791141B2
Source datasetuspto-grants-2014_07
ORD IDord-0a953cd9b52b4e1ea40439fccd633287
Source noteuspto-grants-2014_07