Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2212199생성일: 2026년 10월 26일
Phenylmethanesulfonyl chloride → 9-Chloro-3-methyl-5-(1-phenylmethanesulfonyl-piperidin-3-yl)-5H-isoxazolo[4,3-c]quinolin-4-one
https://huagongshe.com/reaction/2212199
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Phenylmethanesulfonyl chloride | HCID 74740 | — |
| 반응물 | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| 반응물 | 9-Chloro-3-methyl-5-piperidin-3-yl-5H-isoxazolo[4,3-c]quinolin-4-one hydroiodide | HCID 21963712 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 9-Chloro-3-methyl-5-(1-phenylmethanesulfonyl-piperidin-3-yl)-5H-isoxazolo[4,3-c]quinolin-4-one | HCID 21963723 | 73% |
반응 단계
To a 0° C. suspension of 9-chloro-3-methyl-5-piperidin-3-yl-5H-isoxazolo[4,3-c]quinolin-4-one hydroiodide (50 mg, 0.11 mmol) in ethanol (5 mL) add 1,8-diazabicyclo[5.4.0]undec-7-ene (42 μL, 0.28 mmol). Stir the solution for 10 mins. To the solution add α-toluene-sulfonyl chloride (21 mg, 0.11 mmol) and stir the reaction at 0° C. under nitrogen for 30 minutes. Quench the reaction with 1N HCl, concentrate, and extract with 20% isopropanol/chloroform (×2). Wash the combined organic layers with saturated aqueous sodium bicarbonate solution, brine, dry over magnesium sulfate and concentrate. Purify by flash chromatography on silica gel (eluting with 0–0.4% methanol/chloroform) to give 37.9 mg of the title compound as a white solid, 72% yield. 1H NMR: consistent with structure. MS (ion spray) 472 (M+).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07101891B2 |
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| 출처 데이터셋 | uspto-grants-2006_09 |
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| ORD ID | ord-606f274b3ba447d89bb53890261a59cd |
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| 출처 메모 | uspto-grants-2006_09 |
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