Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591935Generated: October 25, 2026

Potassium Carbonate → 2-[2-(3,5-Bis-trifluoromethyl-benzenesulfonylamino)-6,7-dihydro-4H-thiazolo-[5,4-c]pyridin-5-yl]-4-trifluoromethyl-benzamide

https://huagongshe.com/reaction/1591935

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Fluoro-4-(trifluoromethyl)benzamideHCID 605689—
ReactantHCID 86608857HCID 86608857—
SolventDimethyl SulfoxideHCID 679—
SolventMethanolHCID 887—
Product2-[2-(3,5-Bis-trifluoromethyl-benzenesulfonylamino)-6,7-dihydro-4H-thiazolo-[5,4-c]pyridin-5-yl]-4-trifluoromethyl-benzamideHCID 9938946—

Reaction Steps

3.3 g of 2-(3,5-bis-trifluoromethyl-benzenesulfonylamino)-4,5,6,7-tetrahydro-thiazolo[5,4-c]pyridin-5-ium hydrochloride, 1.545 g of 2-fluoro-4-trifluoromethyl-benzamide and 3.3 g of K2CO3 are heated in DMSO at 150° for 5 hours. From the mixture obtained solvent is evaporated, the evaporation residue obtained is dissolved in EtAc/MeOH (9/1) and the mixture obtained is extracted with 50 ml of 1 M HCl and brine. Two phases are obtained and are separated and the organic layer obtained is concentrated and subjected to chromatography. 2-[2-(3,5-Bis-trifluoromethyl-benzenesulfonylamino)-6,7-dihydro-4H-thiazolo-[5,4-c]pyridin-5-yl]-4-trifluoromethyl-benzamide is obtained and is re-crystallized from EtAc.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07291734B2
Source datasetuspto-grants-2007_11
ORD IDord-5d4c0a5163f641aa86ec465296a18c0c
Source noteuspto-grants-2007_11