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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 419407Generated: October 29, 2026

Methyl vinyl sulfone → 1-{4-[3-(Methyloxy)-4-nitrophenyl]-3-cyclohexen-1-yl}-4-[2-(methylsulfonyl)-ethyl]piperazine

https://huagongshe.com/reaction/419407

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl vinyl sulfoneHCID 19354—
Reactant1-{4-[3-(Methyloxy)-4-nitrophenyl]-3-cyclohexen-1-yl}piperazineHCID 59452600—
Solvent1,4-DioxaneHCID 31275—
Product1-{4-[3-(Methyloxy)-4-nitrophenyl]-3-cyclohexen-1-yl}-4-[2-(methylsulfonyl)-ethyl]piperazineHCID 5945259183%

Reaction Conditions

Temperature95 °C

Reaction Steps

A solution of methyl vinyl sulfone (201 mg, 1.89 mmol) and 1-{4-[3-(methyloxy)-4-nitrophenyl]-3-cyclohexen-1-yl}piperazine (200 mg, 0.63 mmol) was stirred in dioxane (6 mL) under N2. The reaction was then heated to 95° C. and stirred for approximately 3 h. The reaction was then cooled to rt and concentrated under vacuum. The residue was taken up in DCM and aqueous (saturated) NaHCO3. The aqueous layer was extracted with DCM (2×). The combined organic layers were dried over MgSO4, filtered, then concentrated and purified by silica gel chromatography to give the title compound of step G (222 mg, 0.52 mmol, 83%) as a light yellow solid. MS (ESI): 424 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093239B2
Source datasetuspto-grants-2012_01
ORD IDord-6c7389cb3b414f4ba201dcdabbfa96e4
Source noteuspto-grants-2012_01