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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177857Generated: November 2, 2026

Hydrochloric Acid → HCID 57855648, compound

https://huagongshe.com/reaction/1177857

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-(Phenylamino)benzoic acidHCID 292331—
ReactantHCID 66953444HCID 66953444—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 57855648HCID 5785564852%

Reaction Steps

DIPEA (74 mg, 0.1 mL, 0.63 mmol) was added drop wise to 4-(phenyl-amino)-benzoic acid (45 mg, 0.21 mmol) in DMF (5 mL). EDCI (100 mg, 0.52 mmol) and HOBT (34 mg, 0.25 mmol) were added consecutively and, after 10 minutes, 2-amino-1-[4-(2-chloro-5-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethanone in its HCl salt form (97 mg, 0.25 mmol) was added. The resulting mixture was stirred at room temperature overnight. 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 get the residue. The obtained residue was purified by column chromatography (using silica gel of 60-120 mesh and 70% EtOAc in Hexane as eluent) to afford 60 mg (52% yield) of N-{2-[4-(2-chloro-5-trifluoromethyl-benzoyl)-piperazin-1-yl]-2-oxo-ethyl}-4-phenylamino-benzamide. LC-MS purity: 98.43%. 1H-NMR (DMSO-d6): δ 8.6 (s, 1H), 8.3 (t, 1H), 7.9 (d, 1H), 7.8 (m, 4H), 7.3 (t, 2H), 7.2 (d, 2H), 7.1 (d, 2H), 6.9 (t, 1H), 4.1 (dd, 2H), 3.6 (m, 6H), 3.2 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842696B2
Source datasetuspto-grants-2010_11
ORD IDord-b03b41ea0f3f4c69b6a175fbe697cda2
Source noteuspto-grants-2010_11