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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1928296Generated: October 30, 2026

Trifluoroacetic acid → 3-{4-[6-Methyl-4-(4-trifluoromethyl-phenyl)-pyridin-2-yl]-pyrimidin-2-yl}-benzenesulfonamide

https://huagongshe.com/reaction/1928296

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantN-tert-butyl-3-{4-[6-methyl-4-(4-trifluoromethylphenyl)-pyridin-2-yl]-pyrimidin-2-yl}-benzenesulfonamideHCID 24760736—
SolventDichloromethaneHCID 6344—
Product3-{4-[6-Methyl-4-(4-trifluoromethyl-phenyl)-pyridin-2-yl]-pyrimidin-2-yl}-benzenesulfonamideHCID 2476073958.3%

Reaction Steps

To a cooled and stirred solution of N-tert-butyl-3-{4-[6-methyl-4-(4-trifluoromethyl-phenyl)-pyridin-2-yl]-pyrimidin-2-yl}-benzenesulfonamide (example 262) (0.480 g, 0.912 mmol) in dichloromethane (10 mL) was added TFA (10 mL) and the reaction mixture was allowed to stir at room temperature for 15 h. The mixture was evaporated to dryness and saturated NaHCO3 solution (5 mL), diethyl ether and heptane were added. The mixture was stirred at room temperature for 1 h, the precipitate was collected by filtration, washed with water and heptane/diethyl ether and dried to yield the title compound as a white solid (0.25 g, 46%). MS (ISP) 469.3 [(M+H)+]; mp>250° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183262B2
Source datasetuspto-grants-2012_05
ORD IDord-95695ec299aa4e7b855335bd425d3b05
Source noteuspto-grants-2012_05