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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1178093Generated: October 31, 2026

1-Hydroxybenzotriazole → HCID 57855638, compound

https://huagongshe.com/reaction/1178093

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant2-(Trifluoromethoxy)benzoic acidHCID 2777223—
ReactantBiphenyl-4-carboxylicacid (2-oxo-2-piperazin-1-yl-ethyl)-amideHCID 57855677—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 57855638HCID 5785563834.1%

Reaction Steps

DIPEA (149.8 mg, 1.15 mmol) was added to a stirred solution of 2-trifluoromethoxy-benzoic acid (53.09 mg, 0.26 mmol) in DMF (3 mL), HOBt (38.2 mg, 0.28 mmol) and EDCI.HCl (123.4 mg, 0.64 mmol) at room temperature. After 2 minutes biphenyl-4-carboxylicacid (2-oxo-2-piperazin-1-yl-ethyl)-amide (100 mg, 0.31 mmol) was added and the resulting mixture was stirred at room temperature overnight. Cold water was then added, and the resulting precipitate was filtered. The residue was purified by column chromatography (using 60-120 mesh silica gel and 50% EtOAc in hexane as eluent) to afford 45 mg (34.1% yield) of biphenyl-4-carboxylicacid {2-oxo-2-[4-(2-trifluoromethoxy-benzoyl)-piperazin-1-yl]-ethyl}-amide, LC-MS purity: 99.18%, 1H NMR: (DMSO) δ 8.7 (s, 1H), 8.0 (s, 2H), 7.8 (s, 4H), 7.4 (s, 7H), 4.2 (d, 2H), 3.8-3.4 (m, 6H), 3.2 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842696B2
Source datasetuspto-grants-2010_11
ORD IDord-c57bd6604ee34aa0a11e76cfd40c1054
Source noteuspto-grants-2010_11