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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1442395Generated: November 3, 2026

1-(2-Hydroxyethyl)piperazine → HCID 9961304, compound

https://huagongshe.com/reaction/1442395

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Hydroxyethyl)piperazineHCID 7677—
ReactantSodium HydroxideHCID 14798—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 68535853HCID 68535853—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 9961304HCID 996130414.5%

Reaction Steps

To a solution of 3-(2,3,4,6-tetra-O-acetyl-β-D-galacto-pyranosyloxy)-4-[(4-{3-[1-carboxy-1-(methyl)ethyl-carbamoyl]propyl}phenyl)methyl]-5-isopropyl-1H-pyrazole (30 mg) in N,N-dimethylformamide (0.5 mL) were added 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (12 mg), 1-hydroxybenzotriazole (9 mg) and 1-(2-hydroxyethyl)piperazine (54 mg), and the mixture was stirred at room temperature overnight. To the reaction mixture was added 5 mol/L aqueous sodium hydroxide solution (0.25 mL), and the resulting mixture was stirred at room temperature for 1 hour. To the reaction mixture was added acetic acid (0.1 mL), and the mixture was diluted with water (1 mL). The insoluble material was removed by filtration, and the filtrate was purified by preparative reverse phase column chromatography (Shiseido CAPCELL PAK UG120 ODS, 5 μL, 120 Å, 20×50 mm, flow rate 30 mL/minute linear gradient, water/acetonitrile=90/10-10/60) to give the title compound (4 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07655632B2
Source datasetuspto-grants-2010_02
ORD IDord-57a9bde45b734bb2b4739db814d965b4
Source noteuspto-grants-2010_02