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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1358050Generated: October 26, 2026

1-Acetylpiperazine → HCID 18186383, compound

https://huagongshe.com/reaction/1358050

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-AcetylpiperazineHCID 83795—
ReactantBinap, (A+-)-HCID 634876—
ReactantHCID 18186409HCID 18186409—
ReactantSodium t-butoxideHCID 23676156—
CatalystDibenzalacetone palladiumHCID 72499888—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 18186383HCID 1818638341.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 1-(4-bromobenzyl)-6-phenylmethoxy-2-(4-fluorophenyl)-1,2,3,4-tetrahydroisoquinoline (1.0 g, 1.99 mmol), dibenzylideneacetone palladium (36 mg, 0.04 mmol), BINAP (74 mg, 0.12 mmol), sodium tert-butoxide (0.29 g, 3.0 mmol) and N-acetylpiperazine (0.38 g, 3.0 mmol) in 2 ml of toluene were added to a sealed tube under an argon atmosphere and heated at 80° C. for 16 h. The sealed tube was cooled to room temperature and the contents of the tube transferred to a separatory funnel. Ethyl acetate and water were added and the organic layer was separated. The combined organic layers were dried over MgSO4, concentrated, and purified by column chromatography (SiO2, chloroform/methanol, 99:1) to provide the title compound (0.45 g, 41% yield): ES-MS (m/z) 550 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06593322B1
Source datasetuspto-grants-2003_07
ORD IDord-34f61fe4560b42608aec614caedc713a
Source noteuspto-grants-2003_07