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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177969Generated: October 26, 2026

1-Hydroxybenzotriazole → 4-Phenyl-thiophene-2-carboxylic acid {2-oxo-2-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethyl}-amide

https://huagongshe.com/reaction/1177969

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Phenylthiophene-2-carboxylic acidHCID 1223184—
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—
Product4-Phenyl-thiophene-2-carboxylic acid {2-oxo-2-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethyl}-amideHCID 2516492435.7%

Reaction Steps

DIPEA (76 mg, 0.59 mmol) was added to a stirred solution of 2-amino-1-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethanone TFA salt (100 mg, 0.24 mmol) in DMF (1 mL). HOBT (32 mg, 0.24 mmol) and EDCI.HCl (45 mg, 0.24 mmol) were then added at room temperature. After 2 minutes, 4-phenyl-thiophene-2-carboxylic acid (40 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 35 mg (35.7% yield) of 4-phenyl-thiophene-2-carboxylic acid {2-oxo-2-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethyl}-amide. LCMS Purity %: 99.1%, 1H NMR (DMSO-d6): δ 8.7 (t, 1H), 8.3 (s, 1H), 8.1 (s, 1H), 7.9-7.6 (m, 5H), 7.6-7.5 (m, 1H), 7.5-7.4 (t, 2H), 7.4-7.3 (m, 1H), 4.2 (m, 2H), 3.7-3.5 (m, 4H), 3.4 (m, 4H), 3.2-3.1 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842696B2
Source datasetuspto-grants-2010_11
ORD IDord-994608dbf4d14277a2c06664004e9962
Source noteuspto-grants-2010_11