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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 878327Generated: October 31, 2026

3-Methanesulfonyl-5-(trifluoromethyl)benzoic acid → N-[4-(2-Chloro-phenyl)-pyridin-3-yl]-3-methanesulfonyl-N-(2,2,2-trifluoro-ethyl)-5-trifluoromethyl-benzamide

https://huagongshe.com/reaction/878327

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Methanesulfonyl-5-(trifluoromethyl)benzoic acidHCID 21544516—
Reactant[4-(2-Chloro-phenyl)-pyridin-3-yl]-(2,2,2-trifluoro-ethyl)-amineHCID 70663252—
ProductN-[4-(2-Chloro-phenyl)-pyridin-3-yl]-3-methanesulfonyl-N-(2,2,2-trifluoro-ethyl)-5-trifluoromethyl-benzamideHCID 86670815—

Reaction Steps

The title compound was prepared in analogy to example 90, from 4-(2-chlorophenyl)-N-(2,2,2-trifluoroethyl)pyridin-3-amine and 3-(methylsulfonyl)-5-(trifluoromethyl)benzoic acid (example 114, intermediate a) after a reaction time of 18 hours at room temperature. The compound was purified by silica gel chromatography on a 20 g column using an MPLC (Flashmaster) system eluting with a gradient of n-heptane:EtOAc (100:0 to 0:100). Further purification by preparative HPLC (Gemini NX) with a gradient of MeOH:water (containing 0.05% formic acid) (80:20 to 98:2). Colorless solid (31%). MS (ESI): m/z=537.045 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987307B2
Source datasetuspto-grants-2015_03
ORD IDord-4c8af4bd929c47fab7e4e56d5cb83955
Source noteuspto-grants-2015_03