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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177955Generated: October 31, 2026

4-(Trifluoromethyl)benzoic acid → HCID 25164520, compound

https://huagongshe.com/reaction/1177955

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethyl)benzoic acidHCID 9966—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant2-amino-1-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethanone TFA saltHCID 86634088—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 25164520HCID 2516452050%

Reaction Steps

DIPEA (50 mg, 0.39 mmol) was added to a stirred solution of 2-amino-1-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethanone TFA salt (68 mg, 0.16 mmol) in DMF (1 mL). HOBT (21 mg, 0.16 mmol) and EDCI.HCl (30 mg, 0.16 mmol) were then added at room temperature. After 2 minutes, 4-trifluoromethylbenzoic acid (25 mg, 0.13 mmol) was added and the resulting mixture was stirred at room temperature for 4 hrs. Cold water (20 mL) was then added and the product was extracted with EtOAc and the organic layer was washed with brine. The organic phase was dried over Na2SO4 and concentrated under reduced pressure. the resulting residue was purified by column chromatography (using silica gel 60-120 mesh and 1% methanol in chloroform as eluent) to afford 28 mg (50% yield) of N-{2-Oxo-2-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethyl}-4-trifluoromethyl-benzamide. LCMS Purity: 92.7%, 1H NMR (CDCl3): δ 8.0-7.9 (m, 2H), 7.8-7.7 (m, 3H), 7.6 (m, 2H), 7.4-7.3 (d, 1H), 4.4-4.3 (dd, 1H), 4.3-4.2 (dd, 1H), 4.0 (m, 2H), 3.8-3.5 (m, 4H), 3.4 (t, 1H), 3.3-3.2 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842696B2
Source datasetuspto-grants-2010_11
ORD IDord-b8aec16cae6d4532bf4154903bb907fe
Source noteuspto-grants-2010_11