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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1665616Generated: October 30, 2026

1-Hydroxybenzotriazole → HCID 44231208, compound

https://huagongshe.com/reaction/1665616

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant5-Phenyl-2-pyridinamineHCID 105097—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant3-Oxo-3-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-propionic acidHCID 57875811—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 44231208HCID 44231208—

Reaction Conditions

Temperature10 °C

Reaction Steps

HOBt (57 mg, 0.42 mmol) and DMAP (46 mg, 0.38 mmol) were added to a stirred solution of 3-oxo-3-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-propionic acid (60 mg, 0.35 mmol) in DMF (2 mL). The reaction mixture was cooled to 10° C. and EDCI.HCl (81 mg, 0.42 mmol) followed by 5-phenyl-pyridin-2-ylamine (120 mg, 0.35 mmol) were added. The reaction mixture was stirred at the room temperature overnight, then diluted with water and the product extracted with ethyl acetate. The ethyl acetate was washed with brine solution, dried over Na2SO4 and evaporated. The residue was purified by column chromatography using silica gel 60-120 mesh and 80% ethyl acetate in hexane as the eluant to afford 65 mg (38% 0 of 3-oxo-N-(5-phenyl-pyridin-2-yl)-3-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-propionamide. LCMS: 497.18 (M+1)+, 90.4%, 1H NMR: (CDCl3): δ 9.6 (d, 1H), 8.5 (s, 1H), 8.2 (m, 1H), 7.9 (m, 1H), 7.75 (d, 1H), 7.6 (m, 4H), 7.45 (t, 2H), 7.35 (m, 2H), 4.0 (m, 2H), 3.7 (m, 3H), 3.55 (m, 4H), 3.26 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08039463B2
Source datasetuspto-grants-2011_10
ORD IDord-9ce614309ead4693bd855573b604e708
Source noteuspto-grants-2011_10