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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 419666생성일: 2026년 10월 25일

Potassium Carbonate → 1-[2-Methyl-5-(ethyloxy)-4-nitrophenyl]-4-[2-(methylsulfonyl)ethyl]piperazine

https://huagongshe.com/reaction/419666

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물1-Ethoxy-5-fluoro-4-methyl-2-nitrobenzeneHCID 59452883—
반응물1-[2-(Methylsulfonyl)ethyl]piperazine hydrochlorideHCID 66649667—
용매Dimethyl SulfoxideHCID 679—
용매DichloromethaneHCID 6344—
생성물1-[2-Methyl-5-(ethyloxy)-4-nitrophenyl]-4-[2-(methylsulfonyl)ethyl]piperazineHCID 5945273490.6%

반응 조건

온도100 °C

반응 단계

1-Methyl-2-fluoro-4-(ethyloxy)-5-nitrobenzene (Example 215, step A) (5.74 g, 28.8 mmol) was dissolved in DMSO (60 mL). K2CO3 (11.9 g, 86.4 mmol) and 1-[2-(methylsulfonyl)ethyl]piperazine hydrochloride (Example 148, step B) (9.85 g, 43.2 mmol) were added and the reaction mixture was heated to 100° C. and allowed to stir overnight. The mixture was cooled to rt then diluted with DCM and filtered. The filtrate was poured into H2O and extracted with DCM. The combined organics were dried with MgSO4, filtered, and concentrated in vacuo to give the title compound of Step A (9.70 g, 26.1 mmol, 90%) as an orange solid. 1H NMR (400 MHz, CDCl3) δ 7.75 (s, 1H), 6.51 (s, 1H), 4.11 (q, J=7.0 Hz, 2H), 3.16 (t, J=6.5 Hz, 2H), 3.03 (s, 3H), 3.00-2.91 (m, 6H), 2.72-2.62 (m, 4H), 2.21 (s, 3H), 1.44 (t, J=7.0 Hz, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08093239B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-5c424a4468b349a1b55325fe61d26e26
출처 메모uspto-grants-2012_01