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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1994134Generated: November 1, 2026

3-(Trifluoromethyl)aniline → HCID 58674630, compound

https://huagongshe.com/reaction/1994134

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethyl)anilineHCID 7375—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 58674341HCID 58674341—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 58674630HCID 5867463032%

Reaction Steps

A solution of 3-[4-({2-[(methylamino)carbonyl]pyridin-4-yl}oxy)phenyl]-propanoic acid (270 mg, 0.90 mmol), 3-(trifluoromethyl)aniline (158 mg, 0.98 mmol), HATU (409 mg, 1.07 mmol), and DIPEA (348 mg, 2.69 mmol) in DMF (5 mL) was stirred at rt for 16 h. The reaction mixture was diluted with EtOAc and washed with 1N HCl and brine. The organic solution was dried over MgSO4, filtered, and concentrated to give A-4 as a white solid (127 mg, 32%). 1H NMR (300 MHz, d6-DMSO) δ: 10.28 (s, 1H), 8.76 (m, 1H), 8.47 (d, 1H), 8.08 (br s, 1H), 7.75 (br d, 1H), 7.53 (t, 1H), 7.31-7.42 (m, 4H), 7.08-7.19 (m, 3H), 2.97 (t, 2H), 2.76 (d, 3H), and 2.71 (d, 2H). LCMS, FA: Rt=1.89 min, [MH+ 444.1].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652041B2
Source datasetuspto-grants-2010_01
ORD IDord-74ca5190b1dc441491996897dd72b93c
Source noteuspto-grants-2010_01