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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177950Generated: October 29, 2026

4-Benzoylbenzoic acid → HCID 25164320, compound

https://huagongshe.com/reaction/1177950

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Benzoylbenzoic acidHCID 69147—
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 25164320HCID 2516432051.9%

Reaction Steps

DIPEA (77 mg, 0.103 mL, 0.60 mmol) was added to a stirred solution of 2-amino-1-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethanone TFA salt (102 mg, 0.29 mmol) in DMF (1 mL). HOBT (32 mg, 0.29 mmol) and EDCI.HCl (46 mg, 0.29 mmol) were then added at room temperature. After 2 minutes, 4-benzoylbenzoic acid (45 mg, 0.20 mmol) was added and the resulting mixture was stirred at room temperature for 4 hrs. Cold water 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 to afford 54 mg (51.9% yield) of 4-benzoyl-N-{2-oxo-2-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethyl}-benzamide. LCMS Purity %: 91.57, HPLC Purity: 95.52%, 1H NMR (DMSO-d6): δ 8.8 (t, 1H), 8.1-8.0 (d, 2H), 7.9-7.64 (m, 7H), 7.6 (t, 3H), 4.3-4.1 (m, 2H), 3.8-3.5 (m, 4H), 3.5-3.4 (m, 2H), 3.2-3.1 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842696B2
Source datasetuspto-grants-2010_11
ORD IDord-bb0cffb9991d47f8a8e8ddec61029938
Source noteuspto-grants-2010_11