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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 75567생성일: 2026년 10월 25일

Hexachloroethane → 6-Fluoro-3-isopropyl-[1,2,4]triazolo[4,3-a]pyridine

https://huagongshe.com/reaction/75567

반응식

참여 물질

역할이름HCID투입량
반응물HexachloroethaneHCID 6214—
반응물TriethylamineHCID 8471—
반응물TriphenylphosphineHCID 11776—
반응물Isobutyric acid N'-(5-fluoro-pyridin-2-yl)-hydrazideHCID 66977821—
용매TetrahydrofuranHCID 8028—
생성물6-Fluoro-3-isopropyl-[1,2,4]triazolo[4,3-a]pyridineHCID 58783963—

반응 단계

To a solution of Intermediate 1e (1.81 g, 9.18 mmol), triphenylphosphine (4.83 g, 18.4 mmol), and triethylamine (5.12 mL, 36.7 mmol) in THF (25 mL) at 0° C., hexachloroethane (4.36 g, 18.4 mmol) was added in 2 portions at a 1 min intervals. The resulting pale brown solution was allowed to warm to RT then stirred for 2 h. The resulting yellow suspension was filtered, washing with THF (2×25 mL). The combined organics were purified using SCX-2 cartridge (washed with DCM-MeOH (1:1, 100 mL) and MeOH (50 mL), and then the product was eluted with 2M NH3 in MeOH) to give a pale yellow solid (1.60 g, 97%, contaminated with ˜2.5% Ph3P═O). 1H NMR (400 MHz, CDCl3): 1.53 (6H, d), 3.32 (1H, sept), 7.15 (1H, ddd), 7.75 (1H, ddd), 7.84 (1H, m).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08835431B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-1af7344cea8a47188f6f1c9e0bb1b5db
출처 메모uspto-grants-2014_09