Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1964생성일: 2026년 10월 24일
(Diethylamino)sulfur trifluoride → 5,6,7,8 tetrahydro-2-[2,4-dichloro-5-(2-propynyloxy)phenyl]-6-fluoro-1,2,4-triazolo[4,3-alpha]pyridin-3(2H)-one
https://huagongshe.com/ko/reaction/1964
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | (Diethylamino)sulfur trifluoride | HCID 123472 | — |
| 반응물 | 5,6,7,8-tetrahydro-2-[2,4-dichloro-5-(2-propynyloxy)phenyl]-6-hydroxy-1,2,4-triazolo[4,3-a]pyridin-3(2H)-one | HCID 19689066 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 5,6,7,8 tetrahydro-2-[2,4-dichloro-5-(2-propynyloxy)phenyl]-6-fluoro-1,2,4-triazolo[4,3-alpha]pyridin-3(2H)-one | HCID 131720564 | 37.7% |
반응 단계
To a solution of 169 mg (0.477 mmol) of 5,6,7,8-tetrahydro-2-[2,4-dichloro-5-(2-propynyloxy)phenyl]-6-hydroxy-1,2,4-triazolo[4,3-a]pyridin-3(2H)-one in 5 mL of dichloromethane was added 76 μl (0.573 mmol) of diethylaminosulfur trifluoride (DAST) at 0° C. The reaction mixture was stirred at 0° C. for 1h. The mixture was then quenched with ice and extracted with dichloromethane. The organic extracts were dried (MgSO4), and then concentrated in vacuo to give a pale red solid. The crude product was purified by flash chromatography over silica gel, eluting with a 95:5 v:v mixture of dichloromethane and methanol to give 64 mg of the title product as a pale yellow foam. 19F NMR (CDCl3, 400 MHz) δ-188 ppm, 1H NMR (CDCl3, 400 MHz) δ 7.5 (s,1H), 7.1 (s,1H), 5.2 (m,1H), 4.8 (s,2H), 4.2-3.6 (m,2H), 3.2-3.0 (m,1H), 3.0-2.6 (m,1H), 2.5 (s,1H), 2.3-1.8 (m,2H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05728651 |
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| 출처 데이터셋 | uspto-grants-1998_03 |
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| ORD ID | ord-9634d1d63f934be6bfca6b1b336ece9e |
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| 출처 메모 | uspto-grants-1998_03 |
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