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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl vinyl sulfone | HCID 19354 | — |
| Reactant | 1-{4-[3-(Methyloxy)-4-nitrophenyl]-3-cyclohexen-1-yl}piperazine | HCID 59452600 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 1-{4-[3-(Methyloxy)-4-nitrophenyl]-3-cyclohexen-1-yl}-4-[2-(methylsulfonyl)-ethyl]piperazine | HCID 59452591 | 83% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08093239B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-6c7389cb3b414f4ba201dcdabbfa96e4 |
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| Source note | uspto-grants-2012_01 |
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