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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethyl Sulfoxide | HCID 679 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 1-Chloro-2-fluoro-4-methoxy-5-nitrobenzene | HCID 53403289 | — |
| 반응물 | 1-[2-(Methylsulfonyl)ethyl]piperazine hydrochloride | HCID 66649667 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 1-[2-Chloro-5-(methyloxy)-4-nitrophenyl]-4-[2-(methylsulfonyl)ethyl]piperazine | HCID 59452634 | 91.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08093239B2 |
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| 출처 데이터셋 | uspto-grants-2012_01 |
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| ORD ID | ord-86d4005b11134c4792f37dc014c8d999 |
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| 출처 메모 | uspto-grants-2012_01 |
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