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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1020749Generated: October 29, 2026

1-Methylpiperazine → HCID 66797580, compound

https://huagongshe.com/reaction/1020749

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2-(Di-tert-butylphosphino)biphenylHCID 2734215—
ReactantHCID 86663332HCID 86663332—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 66797580HCID 66797580—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of Trifluoro-methanesulfonic acid 3-((R)-1-tert-butoxycarbonylamino-ethyl)-phenyl ester (0.340 g, 0.921 mmol), 1-methylpiperazine (0.37 g, 3.68 mmol), Pd2(dba)3 (0.042 g, 0.046 mmol), 2-(di-tert-butylphosphino)-biphenyl (0.054 g, 0.184 mmol), and potassium phosphate (0.273 g, 1.29 mmol) in 20 mL of 1,4 dioxane was heated at 80° C. in a sealed tube for 12 hours. After completion of the reaction, the reaction mixture was cooled to room temperature and diluted with ethyl acetate (100 mL) and the washed with water (20 mL). The aqueous layer was extracted with ethyl acetate (2×50 mL), and the combined organic layers were dried over magnesium sulfate and concentrated in vacuo to afford the crude title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716473B2
Source datasetuspto-grants-2014_05
ORD IDord-8a0944a007084383b548351bbb5f7d59
Source noteuspto-grants-2014_05