Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010708Generated: October 28, 2026

3-(Trifluoromethyl)aniline → HCID 11852874, compound

https://huagongshe.com/reaction/1010708

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethyl)anilineHCID 7375—
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
ReactantHCID 67021528HCID 67021528—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 11852874HCID 11852874—

Reaction Steps

0.15 ml of DIEA are added dropwise to a cold (0° C.) mixture of 55 mg of crude (4-imidazo[4,5-c]pyridin-1-yl-phenyl)-acetic acid, 39 mg of 3-aminobenzotrifluoride and 77 mg of TBTU in 0.5 ml of DMF. The mixture obtained is allowed to warm to rt, stirred for 2 hours, diluted with EtOAc and washed with a saturated aqueous solution of NaHCO3, H2O, and brine. The organic phase obtained is dried (Na2SO4), filtered and concentrated in vacuo. The evaporation residue obtained is purified by silica gel column chromatography. 2-(4-Imidazo[4,5-c]pyridin-1-yl-phenyl)-N-(3-trifluoromethyl-phenyl]-acetamide is obtained in the form of a solid: ES-MS: 397.0 [M+H]+; single peak at tR=3.52 min (System 1); Rf=0.18 (CH2Cl2/MeOH, 94:6).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977338B2
Source datasetuspto-grants-2011_07
ORD IDord-4e32b7d7a86b4e9c9e94a5f0a66fb498
Source noteuspto-grants-2011_07