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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | (Diethylamino)sulfur trifluoride | HCID 123472 | — |
| 반응물 | 5,6,7,8-tetrahydro-2-[2,4-dichloro-5-(2-propynyloxy)phenyl]-8-hydroxy-1,2,4-triazolo[4,3-alpha]pyridin-3(2H)-one | HCID 88322986 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 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 | HCID 88323248 | 90.2% |
반응 단계
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
| 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-04601f04a9e04e4b899149b8d86a04b2 |
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| 출처 메모 | uspto-grants-1998_03 |
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