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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 419369생성일: 2026년 10월 25일

Sodium Carbonate → 1-{1-[3-(Methyloxy)-4-nitrophenyl]-4-piperidinyl}-4-[2-(methylsulfonyl)ethyl]piperazine

https://huagongshe.com/reaction/419369

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물Methyl vinyl sulfoneHCID 19354—
반응물1,4-DioxaneHCID 31275—
반응물1-{1-[3-(Methyloxy)-4-nitrophenyl]-4-piperidinyl}piperazineHCID 59860264—
용매MethanolHCID 887—
생성물1-{1-[3-(Methyloxy)-4-nitrophenyl]-4-piperidinyl}-4-[2-(methylsulfonyl)ethyl]piperazineHCID 5986027499.7%

반응 단계

To a suspension of 1-{1-[3-(methyloxy)-4-nitrophenyl]-4-piperidinyl}piperazine (Example 57, step C) (10.0 g, 23.27 mmol) and 1,4-dioxane (400 mL) was added MeOH (˜100 mL) to enhance solubility. Methyl vinyl sulfone (6.1 mL, 69.8 mmol) and Na2CO3 (7.4 g, 69.8 mmol) were added and the resultant mixture was heated at 80° C. overnight (˜16 h). LCMS indicated that the reaction had gone to completion. The solvent was evaporated and the residue was taken up in DCM (300 mL) and filtered to remove salts. The filtrate was concentrated in vacuo to afford the title compound of step A (9.9 g, >95%) which was carried forward with no further purification. MS (ES+, m/z) 427 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08093239B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-c78d686d2e4b48ca923b7580fc38dc53
출처 메모uspto-grants-2012_01