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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2266919Generated: October 27, 2026

Pyridine → 4,5-dichloro-N-[3,3,3-trifluoro-1-(hydroxymethyl)-2-(trifluoromethyl)propyl]thiophene-2-sulfonamide

https://huagongshe.com/reaction/2266919

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant4,5-Dichlorothiophene-2-sulfonyl chlorideHCID 518622—
Reactant3,3,3-Trifluoro-2-(trifluoromethyl)-1-(hydroxymethyl)propylamineHCID 45107971—
SolventTetrahydrofuranHCID 8028—
Product4,5-dichloro-N-[3,3,3-trifluoro-1-(hydroxymethyl)-2-(trifluoromethyl)propyl]thiophene-2-sulfonamideHCID 111894939%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 3,3,3-trifluoro-2-(trifluoromethyl)-1-(hydroxymethyl)propylamine (0.192 g, 0.9 mmol) in THF (1 mL) was stirred under nitrogen at 25° C. Pyridine (0.147 mL, 1.82 mmol) was added followed by 4,5-dichlorothiophene-2-sulfonyl chloride (0.226 g, 0.391 mmol) in THF (1 mL), and the resulting solution stirred for 18 h at 25° C. After concentration, the residue was taken up in EtOAc (15 mL) and washed with 1 N aq. HCl (10 mL), brine (10 mL), and then dried (Na2SO4). After concentration, the crude product was purified by preparatory TLC, eluent: 30:70 EtOAc:hexanes, to provide 4,5-dichloro-N-[3,3,3-trifluoro-1-(hydroxymethyl)-2-(trifluoromethyl)propyl]thiophene-2-sulfonamide as a white solid (0.037 g, 9% yield, racemic mixture). Mass Spectrum (−ESI): 423.9 (M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858658B2
Source datasetuspto-grants-2010_12
ORD IDord-1eaab133644440c2911e4b28f67e72c1
Source noteuspto-grants-2010_12