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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1014256생성일: 2026년 10월 26일

Methyl vinyl sulfone → 1-[2-(Methanesulfonyl)ethyl]-4-(5-methoxy-2-methyl-4-nitrophenyl)piperazine

https://huagongshe.com/reaction/1014256

반응식

참여 물질

역할이름HCID투입량
반응물Methyl vinyl sulfoneHCID 19354—
반응물1-[2-Methyl-5-(methyloxy)-4-nitrophenyl]piperazineHCID 59441832—
용매1,4-DioxaneHCID 31275—
생성물1-[2-(Methanesulfonyl)ethyl]-4-(5-methoxy-2-methyl-4-nitrophenyl)piperazineHCID 5348798460%

반응 조건

온도120 °C

반응 단계

To 1-[2-methyl-5-(methyloxy)-4-nitrophenyl]piperazine (0.300 g, 1.2 mmol) in 10 mL of dioxane was added, ethenyl methyl sulfone (0.32 g, 3 mmol). The mixture was heated to 120° C. 1 hour. The solvent was rotovaped down and the crude product was purified by flash chromatography, followed by a wash of the solids with 30% ether in hexanes to give 1-[2-methyl-5-(methyloxy)-4-nitrophenyl]-4-[2-(methylsulfonyl)ethyl]piperazine (0.257 g, 0.72 mmol, 60%). 1H NMR (400 MHz, CDCl3) δ ppm 7.80 (s, 1 H), 6.54 (s, 1 H), 3.93 (s, 3 H), 3.18-3.30 (m, 2 H), 2.99-3.10 (m, 9 H), 2.71-2.82 (m, 4 H), 2.23 (s, 3 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07981903B2
출처 데이터셋uspto-grants-2011_07
ORD IDord-4fe8b1ddb44a4dcbb90d75658064339d
출처 메모uspto-grants-2011_07