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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 392429Generated: October 25, 2026

Dimethyl Sulfoxide → N-(3-Formylphenyl)-N-(ethanesulfonyl)pyrid-3-ylmethylamine

https://huagongshe.com/reaction/392429

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantNitrogenHCID 947—
ReactantOxalyl chlorideHCID 65578—
ReactantSodium BicarbonateHCID 516892—
Reactantn-(3-Hydroxymethylphenyl)-n-(ethylsulfonyl)pyrid-3-ylmethylamineHCID 23521701—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductN-(3-Formylphenyl)-N-(ethanesulfonyl)pyrid-3-ylmethylamineHCID 235216995.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

Into a −78° C. solution of DMSO (20.8 mL, 0.269 mole, 3.1 eq) in DCM (460 mL) was added oxalyl chloride (16 mL, 0.109 mole, 1.25 eq) dropwise and stirred for 15 minutes. N-(3-(Hydroxymethyl)phenyl)-N-(ethanesulfonyl)pyrid-3-ylmethylamine (26.4 g, 0.86 mole, 1 eq) was added dropwise via addition funnel as a solution in DCM (146 mL). The reaction mixture was stirred for 30 min. then TEA (102 mL, 1 mole, 11.7 eq) was added via addition funnel. The reaction mixture was allowed to warmed to 0° C. with an ice bath and stirred for 1 hour with a N2 sweep through a bleach/caustic scrubber. The reaction mixture was poured into saturated NaHCO3 and diluted with diethyl ether (2000 mL). The layers were separated and the aqueous layer backextracted with diethyl ether (1000 mL). The combined organics were washed with brine (1000 mL), dried with MgSO4, filtered and concentrated. The residue was purified by flash chromatography, eluting with 1:1 DCM/EtOAc to give the title compound as a white solid (15.0 g, 57.2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06800651B2
Source datasetuspto-grants-2004_10
ORD IDord-c11d95ab345a4fae8c2ff97a29698eaf
Source noteuspto-grants-2004_10