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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177888Generated: October 26, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → N-{2-oxo-2-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethyl}-4-pyridin-2-yl-benzamide

https://huagongshe.com/reaction/1177888

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-(2-Pyridyl)Benzoic AcidHCID 821692—
Reactant2-Amino-1-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethanone hydrochlorideHCID 66953178—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductN-{2-oxo-2-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethyl}-4-pyridin-2-yl-benzamideHCID 5785566719.5%

Reaction Steps

DIPEA (116.32 mg, 0.15 mL, 0.9 mmol) was added to a stirred solution of 4-pyridin-2-yl-benzoic acid (60 mg, 0.3 mmol) in DMF (1.5 mL). HOBT (48 mg, 0.36 mmol) and EDCI (70 mg, 0.36 mmol) were then added at room temperature. After 2 minutes 2-amino-1-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethanone hydrochloride salt (127 mg, 0.36 mmol) was added and the resulting mixture was stirred at room temperature overnight. Cold water was then added and then extrated with ethyl acetate. The organic layer was washed with brine and dried over Na2SO4 and concentrated under reduced pressure to afford 29 mg (19.46%) of N-{2-oxo-2-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethyl}-4-pyridin-2-yl-benzamide. LCMS Purity: 89.36%. 1H NMR (DMSO-d6): δ 9-8.9 (d, 1H), 8.6 (d, 1H), 8.5 (m, 1H), 8.2-8.1 (dt, 1H), 8.0 (d, 2H), 7.9-7.6 (m, 5H), 7.6-7.5 (m, 2H), 4.2 (m, 2H), 3.8-3.6 (m, 4H), 3.2-3.4 (m, 2H), 3.2-3 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842696B2
Source datasetuspto-grants-2010_11
ORD IDord-d359ba07ba2a41f8bfa6b5f17eae7216
Source noteuspto-grants-2010_11