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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177989Generated: October 31, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → HCID 59559631, compound

https://huagongshe.com/reaction/1177989

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Chloroisonicotinic acidHCID 236985—
ReactantBiphenyl-4-carboxylicacid (2-oxo-2-piperazin-1-yl-ethyl)-amideHCID 57855677—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 59559631HCID 5955963149.2%

Reaction Steps

DIPEA (179.7 mg, 0.24 mL, 1.39 mmol) was added to a stirred solution of 6-chloro-pyridine-4-carboxylic acid (48.6 mg, 0.37 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 80% EtOAc in Hexane as eluent) to afford 70 mg (49.2% yield) of biphenyl-4-carboxylic acid {2-[4-(2-chloro-pyridine-4-carbonyl)-piperazin-1-yl]-2-oxo-ethyl}-amide. LCMS Purity: 99.47, 1H NMR (DMSO-d6-D2O): δ 8.5 (s, 1H), 7.96-7.86 (d, 2H), 7.8-7.64 (m, 4H), 7.6-7.34 (m, 5H), 4.2-4.06 (dd, 2H), 3.72-3.42 (m, 6H), 3.38-3.2 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842696B2
Source datasetuspto-grants-2010_11
ORD IDord-72b85c5fdc844959863cfd1a33993de2
Source noteuspto-grants-2010_11