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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1665628Generated: October 30, 2026

1-Hydroxybenzotriazole → HCID 66624895, compound

https://huagongshe.com/reaction/1665628

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant6-(Benzyloxy)pyridin-3-amineHCID 563286—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant3-Oxo-3-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-propionic acidHCID 57875811—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 66624895HCID 6662489539.3%

Reaction Conditions

Temperature10 °C

Reaction Steps

HOBt (43 mg, 0.32 mmol) and DIEA (150 mg, 011 mmol) were added to a stirred solution of 3-oxo-3-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-propionic acid (100 mg, 0.29 mmol) in DMF (4 mL). The reaction mixture was cooled to 10° C. and EDCI.HCl (111 mg, 0.58 mmol) followed by 6-benzyloxy-pyridin-3-ylamine (81 mg, 0.4 mmol) were added. The reaction mixture was stirred at room temperature overnight then diluted with water and the product extracted with ethyl acetate. The organics were washed with brine solution, dried over Na2SO4 and concentrated to afford a residue which was purified by column chromatography using silica gel 60-120 mesh (80% ethyl acetate in hexane) to afford 60 mg (39%) of N-(5-benzyloxy-pyridin-2-yl)-3-oxo-3-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-propionamide. LCMS: 527.19 (M+1)+, 98.6%, 1H NMR: (DMSO-d6): δ 10.2 (td, 1H), 8.4 (dd, 1H), 8 (dt, 1H), 7.8 (d, 1H), 7.7 (t, 1H), 7.6 (t, 1H), 7.5 (d, 1H), 7.4 (m, 5H), 6.9 (m, 1H), 5.4 (d, 2H), 3.8 (m, 6H), 3.5 (m, 2H), 3.2 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08039463B2
Source datasetuspto-grants-2011_10
ORD IDord-03b71a6ce32e494185fc753d6d949243
Source noteuspto-grants-2011_10