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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177876Generated: October 26, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → 1-(3-Phenyl-propionyl)-piperidine-4-carboxylic acid {2-oxo-2-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethyl}-amide

https://huagongshe.com/reaction/1177876

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-(3-Phenylpropanoyl)piperidine-4-carboxylic acidHCID 2813193—
Reactant2-amino-1-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethanone TFA saltHCID 86634088—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product1-(3-Phenyl-propionyl)-piperidine-4-carboxylic acid {2-oxo-2-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethyl}-amideHCID 5955957827.8%

Reaction Steps

DIPEA (72.27 mg, 0.09 mL, 0.55 mmol) was added to a stirred solution of 1-(3-phenyl-propionyl)-piperidine-4-carboxylic acid (58.38 mg, 0.22 mmol) in DMF (1 mL). HOBT (30.2 mg, 0.22 mmol) and EDCI (42.76 mg, 0.22 mmol) were then added at room temperature. After 2 minutes, 2-amino-1-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethanone trifluoroacetic acid salt (80 mg, 0.18 mmol) was added and the resulting mixture was stirred at room temperature for 16 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 28 mg (26.89% yield) of 1-(3-phenyl-propionyl)-piperidine-4-carboxylic acid {2-oxo-2-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethyl}-amide, LCMS Purity: 92.41%. 1H NMR (CDCl3): δ 7.8-7.7 (d, 1H), 7.68-7.52 (m, 2H), 7.38-7.28 (m, 2H), 7.26-7.14 (m, 3H), 6.62-6.48 (s, 1H), 4.7-4.55 (d, 1H), 4.2-3.4 (m, 9H), 3.4-3.1 (d, 3H), 3.05-2.85 (t, 3H), 2.7-2.5 (t, 3H), 2.5-2.3 (t, 2H), 1.9-1.3 (t, 2H), 0.9 (d, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842696B2
Source datasetuspto-grants-2010_11
ORD IDord-c4d3fc93e2c5431ca700205830c5be94
Source noteuspto-grants-2010_11