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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177951Generated: October 31, 2026

4-Fluorobenzoic Acid → HCID 59559577, compound

https://huagongshe.com/reaction/1177951

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluorobenzoic AcidHCID 9973—
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 59559577HCID 59559577—

Reaction Steps

DIPEA (46.5 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-fluorobenzoic acid (17 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 34 mg of 4-fluoro-N-{2-oxo-2-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethyl}-benzamide LCMS Purity: 92.29%, HPLC Purity: 93.53%. NMR Values: 1H NMR (DMSO-d6): δ 7.9-7.8 (2H, m), 7.8-7.7 (d, 1H), 7.6 (m, 2H), 7.4-7.3 (d, 1H), 7.3 (t, 2H), 4.3 (dd, 1H), 4.2 (dd, 2H), 4.0 (m, 2H), 3.8-3.6 (m, 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-70c9287a09834a8a9f987937607e3d90
Source noteuspto-grants-2010_11