Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2401030Generated: October 30, 2026

Propargyl alcohol → N-[3-(3-hydroxyprop-1-yn-1-yl)pyrazin-2-yl]-2-(trifluoromethyl)benzenesulfonamide

https://huagongshe.com/reaction/2401030

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl alcoholHCID 7859—
ReactantN-(3-chloropyrazin-2-yl)-2-(trifluoromethyl)benzenesulfonamideHCID 57586069—
ReactantHCID 178476685HCID 178476685—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
ProductN-[3-(3-hydroxyprop-1-yn-1-yl)pyrazin-2-yl]-2-(trifluoromethyl)benzenesulfonamideHCID 5744425148%

Reaction Conditions

Temperature100 °C

Reaction Steps

N-(3-chloropyrazin-2-yl)-2-(trifluoromethyl)benzenesulfonamide (1.35 g; 4.0 mmol; 1.00 eq.) and 2-propyn-1-ol (336 mg; 6.0 mmol; 1.5 eq.) were dissolved in 10 mL of DMF under nitrogen atmosphere. To the reaction mixture was added CH3COOK (588 mg; 6.0 mmol; 1.5 eq.) and Pd(PPh3)4 (232 mg; 0.2 mmol) under nitrogen. The reaction mixture was then heated at 100° C. under nitrogen for 2 hours. After removal of the solvent by distillation in vacuo, the residue was triturated with water (40 mL) and extracted with diethyl ether (3×30 mL). The organic layer was dried over MgSO4 and evaporated down. The crude product was purified by silica gel column chromatography using a mixture of hexane and AcOEt to give pure N-[3-(3-hydroxyprop-1-yn-1-yl)pyrazin-2-yl]-2-(trifluoromethyl)benzenesulfonamide as a yellowish solid (686 mg, 48% yield, 98% HPLC purity).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796280B2
Source datasetuspto-grants-2014_08
ORD IDord-b0430c29c8c943bfb73e798b2c5661c4
Source noteuspto-grants-2014_08