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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

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참여 물질

역할이름HCID투입량
반응물(Diethylamino)sulfur trifluorideHCID 123472—
반응물5,6,7,8-tetrahydro-2-[2,4-dichloro-5-(2-propynyloxy)phenyl]-6-hydroxy-1,2,4-triazolo[4,3-a]pyridin-3(2H)-oneHCID 19689066—
용매DichloromethaneHCID 6344—
생성물5,6,7,8 tetrahydro-2-[2,4-dichloro-5-(2-propynyloxy)phenyl]-6-fluoro-1,2,4-triazolo[4,3-alpha]pyridin-3(2H)-oneHCID 13172056437.7%

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온도0 °C

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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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05728651
출처 데이터셋uspto-grants-1998_03
ORD IDord-9634d1d63f934be6bfca6b1b336ece9e
출처 메모uspto-grants-1998_03