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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1967생성일: 2026년 10월 23일

(Diethylamino)sulfur trifluoride → 5,6,7,8-tetrahydro-2-[2,4-dichloro-5-(2-propynyloxy)phenyl]-8-fluoro-1,2,4-triazolo[4,3-alpha]pyridin-3(2H)-one

https://huagongshe.com/ko/reaction/1967

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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]-8-hydroxy-1,2,4-triazolo[4,3-alpha]pyridin-3(2H)-oneHCID 88322986—
용매DichloromethaneHCID 6344—
생성물5,6,7,8-tetrahydro-2-[2,4-dichloro-5-(2-propynyloxy)phenyl]-8-fluoro-1,2,4-triazolo[4,3-alpha]pyridin-3(2H)-oneHCID 8832324890.2%

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온도-78 °C

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To a solution of 300 mg (0.847 mmol) of 5,6,7,8-tetrahydro-2-[2,4-dichloro-5-(2-propynyloxy)phenyl]-8-hydroxy-1,2,4-triazolo[4,3-α]pyridin-3(2H)-one in 10 mL of dichloromethane was added 123 mL (0.930 mmol) of diethylaminosulfur trifluoride (DAST) at -78° C. The reaction mixture was stirred at -78° C. for 4h. The mixture was warmed to room temperature, quenched with ice, and extracted with dichloromethane. The organic layers were dried (MgSO4), and concentrated under reduced pressure. The crude product was flash chromatographed over silica gel, eluting with a 98:2 v:v mixture of dichloromethane and methanol to give 272 mg of the title product of Step 4 as a yellow solid. 19F NMR (CDCl3, 300 MHz) δ-172; 1H NMR (CDCl3, 300 MHz) δ 7.55 (s,1H), 7.2 (s,1H), 5.6, 5.5 (2m, J=70 Hz,1H), 4.8 (s,2H), 4.0 (m,1H), 3.55 (m,1H), 2.6 (m,1H), 2.5-1.8 (m,4H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05728651
출처 데이터셋uspto-grants-1998_03
ORD IDord-04601f04a9e04e4b899149b8d86a04b2
출처 메모uspto-grants-1998_03