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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 419545Generated: October 30, 2026

1-Iodopropane → 1-[3-(Methyloxy)-4-nitrophenyl]-4-propylpiperazine

https://huagongshe.com/reaction/419545

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-IodopropaneHCID 33643—
ReactantSodium BicarbonateHCID 516892—
Reactant1-(3-Methoxy-4-nitrophenyl)piperazineHCID 3967409—
SolventAcetonitrileHCID 6342—
Product1-[3-(Methyloxy)-4-nitrophenyl]-4-propylpiperazineHCID 5986026635.2%

Reaction Steps

A mixture of 1-[3-(methyloxy)-4-nitrophenyl]piperazine (Example 135, step A) (0.50 g, 2.1 mmol) and 1-iodopropane (0.72 g, 4.22 mmol) was stirred in acetonitrile (42 mL) at rt under N2. To this mixture was added NaHCO3 (0.27 g, 2.5 mmol). The reaction was then heated to reflux and stirred for 24 h. The reaction was cooled to rt, concentrated under vacuum and the residue chromatographed on silica gel to give the title compound of step A (206 mg, 0.74 mmol, 35%) as a yellow oil. MS (ESI): 280 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093239B2
Source datasetuspto-grants-2012_01
ORD IDord-48c86d5449d84da390555cdf20b33c31
Source noteuspto-grants-2012_01