Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1868127생성일: 2026년 10월 27일
Diisopropylethylamine → (R)-4-(4-fluoro-2-(trifluoromethyl)phenyl)-1-(3-methoxyphenylsulfonyl)-2-methylpiperazine
https://huagongshe.com/reaction/1868127
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | 3-Methoxybenzenesulfonyl chloride | HCID 2737504 | — |
| 반응물 | (R)-1-(4-fluoro-2-(trifluoromethyl)phenyl)-3-methylpiperazine | HCID 68554948 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | (R)-4-(4-fluoro-2-(trifluoromethyl)phenyl)-1-(3-methoxyphenylsulfonyl)-2-methylpiperazine | HCID 68551747 | — |
반응 단계
To a stirred solution of (R)-1-(4-fluoro-2-(trifluoromethyl)phenyl)-3-methylpiperazine (5.34 g, 21.86 mmol) in anhydrous dichloromethane (20 mL) was added diisopropylethylamine (10.3 mL, 59.1 mmol) at 0° C. The reaction mixture was stirred at room temperature for 15 minutes then 3-Methoxy benzene sulfonyl chloride (2.44 g, 11.82 mmol) dissolved in dichloromethane (10 mL) was introduced dropwise. The cooling bath was removed and the mixture was stirred at room temperature for 0.5 hour. Reaction was complete as determined by TLC. The reaction mixture was diluted with dichloromethane washed with saturated NaHCO3 (aqueous), dried over MgSO4 and concentrated. The crude product was purified via flash column chromatography to yield (R)-4-(4-fluoro-2-(trifluoromethyl)phenyl)-1-(3-methoxyphenylsulfonyl)-2-methylpiperazine in quantitative yield (5.10 g) as a white solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07632838B2 |
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| 출처 데이터셋 | uspto-grants-2009_12 |
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| ORD ID | ord-dfe0489e81be4f3fb842300481b6140d |
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| 출처 메모 | uspto-grants-2009_12 |
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