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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 878148Generated: October 31, 2026

3-Methanesulfonyl-5-(trifluoromethyl)benzoic acid → 3-Methanesulfonyl-N-(2-methoxy-[3,4']bipyridinyl-3'-yl)-N-(2,2,2-trifluoro-ethyl)-5-trifluoromethyl-benzamide

https://huagongshe.com/reaction/878148

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Methanesulfonyl-5-(trifluoromethyl)benzoic acidHCID 21544516—
Reactant(2-Methoxy-[3,4]bipyridinyl-3'-yl)-(2,2,2-trifluoro-ethyl)-amineHCID 70663300—
Product3-Methanesulfonyl-N-(2-methoxy-[3,4']bipyridinyl-3'-yl)-N-(2,2,2-trifluoro-ethyl)-5-trifluoromethyl-benzamideHCID 60198026—

Reaction Steps

The title compound was prepared in analogy to example 90, from (2-methoxy-[3,4′]bipyridinyl-3′-yl)-(2,2,2-trifluoro-ethyl)-amine (example 135, intermediate a) and 3-methanesulfonyl-5-trifluoromethyl-benzoic acid (example 114, intermediate a) after a reaction time of 72 hours. The compound was purified by silica gel chromatography using a MPLC system (CombiFlash Companion, Isco Inc.) eluting with a gradient of CH2Cl2: EtOAc (100:0 to 85:15), followed by preparative HPLC using a gradient of methanol:water (10:50 to 95:5). Light yellow foam (28%). MS (ESI): m/z=534.090 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987307B2
Source datasetuspto-grants-2015_03
ORD IDord-3bc0271955844dbca354d5a5e7a0d683
Source noteuspto-grants-2015_03