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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177988Generated: November 1, 2026

2,6-Difluorobenzoic acid → HCID 59559673, compound

https://huagongshe.com/reaction/1177988

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-Difluorobenzoic acidHCID 9796—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
ReactantBiphenyl-4-carboxylicacid (2-oxo-2-piperazin-1-yl-ethyl)-amideHCID 57855677—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 59559673HCID 5955967339.6%

Reaction Steps

DIPEA (179.7 mg, 0.24 mL, 1.39 mmol) was added to a stirred solution of 2,6-difluoro-benzoic acid (48.8 mg, 0.30 mmol) in DMF (3 mL). HOBT (45.9 mg, 0.34 mmol) and EDCI (148.1 mg, 0.77 mmol) were then added at room temperature. After 2 minutes, Biphenyl-4-carboxylic acid (2-oxo-2-piperazin-1-yl-ethyl)-amide (120 mg, 0.37 mmol) was added and 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 60% EtOAc in Hexane as eluent) to afford 55 mg (38.4% yield) of biphenyl-4-carboxylic acid {2-[4-(2,6-difluoro-benzoyl)-piperazin-1-yl]-2-oxo-ethyl}-amide. LCMS Purity: 99.12%. 1H NMR (DMSO-d6): δ 8.7-8.6 (t, 1H), 8.0-7.94 (d, 2H), 7.82-7.7 (q, 4H), 7.62-7.54 (m, 1H), 7.54-7.38 (m, 3H), 7.3-7.2 (t, 2H), 4.2 (dd, 2H), 3.8-3.4 (m, 8H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842696B2
Source datasetuspto-grants-2010_11
ORD IDord-bb7021eaf036464e89dcb47f0ea1c3f4
Source noteuspto-grants-2010_11