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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1815193Generated: October 30, 2026

3-(Trifluoromethyl)aniline → STK345463

https://huagongshe.com/reaction/1815193

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethyl)anilineHCID 7375—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Chloronicotinoyl chlorideHCID 2774541—
SolventDichloromethaneHCID 6344—
ProductSTK345463HCID 68366293.3%

Reaction Steps

2-Chloropyridine-3-carbonyl chloride (18.02 g, 0.102 mol) in CH2Cl2 (100 ml) was added dropwise (via an addition funnel) to a stirred solution of 3-(trifluoromethyl)-aniline (15.00 g, 0.093 mol) and DIEA (24.39 ml, 0.14 mol) in CH2Cl2 (500 ml) at 0° C. The mixture gradually was warmed to RT. The reaction continued for 18 h before washing several times with saturated NaHCO3 aqueous solution and brine, respectively. The organic layer was dried over Na2SO4 and evaporated. The resulting oil was purified over silica gel with EtOAc/hexane (2:1) as eluant to leave the amide as a white solid (26.08 g). MS: (ES+) 301 (M+1)+; (ES−): 299 (M−1)−. Calc'd for C13H8ClF3N2O: 300.03.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06878714B2
Source datasetuspto-grants-2005_04
ORD IDord-6ec238ac37664109868ffcbb5427881e
Source noteuspto-grants-2005_04