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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354561Generated: November 1, 2026

Triethylamine → (+)-4-{4-[3-(3-Benzo[1,3]dioxol-5-ylmethyl-piperidin-1-yl)-propionyl]-piperazin-1-yl}-2-fluoro-benzonitrile

https://huagongshe.com/reaction/2354561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-Benzo[1,3]dioxol-5-ylmethyl-piperidineHCID 17039527—
Reactant4-(4-Acryloylpiperazin-1-yl)-2-fluorobenzonitrileHCID 68451897—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product(+)-4-{4-[3-(3-Benzo[1,3]dioxol-5-ylmethyl-piperidin-1-yl)-propionyl]-piperazin-1-yl}-2-fluoro-benzonitrileHCID 12000651—

Reaction Steps

A solution of 4-(4-acryloyl-piperazin-1-yl)-2-fluoro-benzonitrile (0.125 g, 0.48 mmol), (+)-3-benzo[1,3]dioxol-5-ylmethyl-piperidine (0.106 g, 0.48 mmol) and triethylamine (0.088 ml, 0.629 ml) in THF (1.6 ml) is stirred at rt for 25 h. The mixture is diluted with CH2Cl2 and washed with sat. aq. Na2CO3 solution The organic layer is separated off, dried over Na2SO4 and evaporated. The residue is purified by MPLC (60 g silica gel, eluent CH2Cl2:MeOH 9:1) to give the title compound, (+)-4-{4-[3-(3-benzo[1,3]dioxol-5-ylmethyl-piperidin-1-yl)-propionyl]-piperazin-1-yl}-2-fluoro-benzonitrile, as a colourless foam:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07754719B2
Source datasetuspto-grants-2010_07
ORD IDord-70f296480ab64e799f1e9dcefb154d27
Source noteuspto-grants-2010_07