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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177984Generated: November 2, 2026

3,5-Dichlorobenzoic acid → HCID 59559609, compound

https://huagongshe.com/reaction/1177984

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-Dichlorobenzoic acidHCID 5811—
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 59559609HCID 5955960933.8%

Reaction Steps

DIPEA (149.8 mg, 0.2 mL, 1.15 mmol) was added to a stirred solution of 3,5-dichloro-benzoic acid (49.2 mg, 0.25 mmol) in DMF (3 mL). HOBT (38.2 mg, 0.28 mmol) and EDCI (123 mg, 0.34 mmol) were then added at room temperature. After 2 minutes, Biphenyl-4-carboxylic acid (2-oxo-2-piperazin-1-yl-ethyl)-amide (100 mg, 0.30 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 42 mg (32.8% yield) of biphenyl-4-carboxylic acid {2-[4-(3,5-dichloro-benzoyl)-piperazin-1-yl]-2-oxo-ethyl}-amide. LCMS Purity: 98.36%. 1H NMR (DMSO-d6): δ 8.7-8.62 (t, 1H), 8.0-7.94 (d, 2H), 7.84-7.7 (m, 5H), 7.58-7.46 (m, 4H), 7.44-7.36 (m, 1H), 4.26-4.1 (bs, 2H), 3.74-3.46 (bs, 7H), 3.42-3.34 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842696B2
Source datasetuspto-grants-2010_11
ORD IDord-17a129709da2456a88b80f7bbef542a9
Source noteuspto-grants-2010_11