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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 906281Generated: October 26, 2026

Trifluoroacetic acid → 3'-[4-Difluoromethyl-6-(6-trifluoromethyl-pyridin-3-yl)-pyrimidin-2-yl]-biphenyl-3-sulfonic acid amide

https://huagongshe.com/reaction/906281

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant3'-[4-Difluoromethyl-6-(6-trifluoromethyl-pyridin-3-yl)-pyrimidin-2-yl]-biphenyl-3-sulfonic acid tert-butylamideHCID 67393517—
SolventDichloromethaneHCID 6344—
Product3'-[4-Difluoromethyl-6-(6-trifluoromethyl-pyridin-3-yl)-pyrimidin-2-yl]-biphenyl-3-sulfonic acid amideHCID 2509719581.3%

Reaction Steps

To a cooled and stirred solution of 3′-[4-difluoromethyl-6-(6-trifluoromethyl-pyridin-3-yl)-pyrimidin-2-yl]-biphenyl-3-sulfonic acid tert-butylamide (0.56 g) in dichloromethane (7 ml) was added TFA (7 ml) and the reaction mixture was allowed to stir at room temperature for 15 h. The mixture was evaporated to dryness, poured into 2N Na2CO3 solution (25 ml) and extracted with ethyl acetate (3×50 ml). The combined organic layers were washed with brine (50 ml), dried (MgSO4) and evaporated. Further purification by crystallization (ethyl acetate/heptane) yielded the title compound as a white solid (0.41 g, 81%). MS (ISP) 507.2 [(M+H)+]; mp 222° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08012986B2
Source datasetuspto-grants-2011_09
ORD IDord-c25b4984fd7a4815a3a30419a20e0f09
Source noteuspto-grants-2011_09