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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 419610생성일: 2026년 10월 25일

Dimethyl Sulfoxide → 1-[2-Chloro-5-(methyloxy)-4-nitrophenyl]-4-[2-(methylsulfonyl)ethyl]piperazine

https://huagongshe.com/reaction/419610

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfoxideHCID 679—
반응물Potassium CarbonateHCID 11430—
반응물1-Chloro-2-fluoro-4-methoxy-5-nitrobenzeneHCID 53403289—
반응물1-[2-(Methylsulfonyl)ethyl]piperazine hydrochlorideHCID 66649667—
용매WaterHCID 962—
생성물1-[2-Chloro-5-(methyloxy)-4-nitrophenyl]-4-[2-(methylsulfonyl)ethyl]piperazineHCID 5945263491.3%

반응 조건

온도100 °C

반응 단계

To 1-chloro-2-fluoro-4-(methyloxy)-5-nitrobenzene (Example 104, Step B) (0.822 g, 4.0 mmol), 4-[2-(methylsulfonyl)ethyl]piperazine hydrochloride (Example 148, Step B) (0.915 g, 4.0 mmol), and K2CO3 (1.7 g, 12 mmol) was added DMSO (8 mL). The reaction was heated to 100° C. for two days. The reaction was determined to be complete by TLC. The reaction mixture was diluted with H2O and extracted with DCM and EtOAc sequentially for two iterations. The organic was dried (MgSO4), filtered, and rotovapped down. Purification by flash chromatography provided the title compound of Step A (1.38 g, 91%). MS (M+H, ES+) 378.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08093239B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-86d4005b11134c4792f37dc014c8d999
출처 메모uspto-grants-2012_01