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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 419424Generated: November 1, 2026

Water → 1-{1-[2,5-Bis(methyloxy)-4-nitrophenyl]-4-piperidinyl}-4-(2-fluoroethyl)piperazine

https://huagongshe.com/reaction/419424

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Chloro-2,5-dimethoxy-4-nitrobenzeneHCID 81362—
Reactant1-(2-Fluoroethyl)-4-(4-piperidinyl)piperazineHCID 59452795—
SolventDimethyl SulfoxideHCID 679—
Product1-{1-[2,5-Bis(methyloxy)-4-nitrophenyl]-4-piperidinyl}-4-(2-fluoroethyl)piperazineHCID 5945291975%

Reaction Conditions

Temperature80 °C

Reaction Steps

4-Chloro-2,5-dimethoxynitrobenzene (1.0 g, 4.6 mmol) was dissolved in DMSO (10 mL). K2CO3 (0.953 g, 6.9 mmol) and 1-(2-fluoroethyl)-4-(4-piperidinyl)piperazine (0.989 g, 4.6 mmol) were added and the reaction mixture was heated to 80° C. and allowed to stir for 60 h. The mixture was then poured into H2O and extracted with EtOAc (2×). The combined organics were dried with MgSO4, filtered, and concentrated in vacuo. The resulting residue was adsorbed onto silica gel and flash chromatographed to give the title compound of step E (1.36 g, 75%). MS (M+H, ES+) 397.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093239B2
Source datasetuspto-grants-2012_01
ORD IDord-ca07871b5ba04d9c8a437eaba32ff950
Source noteuspto-grants-2012_01