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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177952Generated: October 31, 2026

4-Nitrobenzoic Acid → HCID 25164321, compound

https://huagongshe.com/reaction/1177952

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrobenzoic AcidHCID 6108—
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 25164321HCID 2516432174%

Reaction Steps

DIPEA (47 mg, 0.36 mmol) was added to a stirred solution of 2-amino-1-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethanone TFA salt (62 mg, 0.14 mmol) in DMF (1 mL). HOBT (19 mg, 0.14 mmol) and EDCI.HCl (28 mg, 0.14 mmol) were then added at room temperature. After 2 minutes, 4-nitrobenzoic acid (20 mg, 0.12 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 to afford 40.7 mg (74% yield) of 4-nitro-N-{2-oxo-2-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethyl}-benzamide. LCMS Purity: 88.6%, 1H NMR (CDCl3): δ 8.3 (d, 2H), 8.0 (m, 2H), 7.8-7.7 (d, 1H), 7.6 (m, 2H), 7.4-7.3 (d, 2H), 4.4-4.3 (dd, 1H), 4.3-4.2 (dd, 2H), 4.1-3.9 (2m, H), 3.8-3.6 (dd, 2H), 3.6-3.5 (m, 2H), 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-14bf6c30cff74cb8a4c9b190431093ec
Source noteuspto-grants-2010_11