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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1369435생성일: 2026년 10월 26일

Cyclobutanone → 6-Chloro-3-(2-fluorophenyl)-7-(1-hydroxycyclobutyl)-1,2,4-triazolo[4,3-b]pyridazine

https://huagongshe.com/reaction/1369435

반응식

참여 물질

역할이름HCID투입량
반응물CyclobutanoneHCID 14496—
반응물6-Chloro-3-(2-fluorophenyl)-7-(trimethylsilyl)-[1,2,4]triazolo[4,3-b]pyridazineHCID 15486175—
촉매1-Butanaminium, N,N,N-tributyl-, (TB-5-11)-difluorotriphenylstannate(1-) (1:1)HCID 178449042—
용매TetrahydrofuranHCID 8028—
생성물6-Chloro-3-(2-fluorophenyl)-7-(1-hydroxycyclobutyl)-1,2,4-triazolo[4,3-b]pyridazineHCID 2260991026%

반응 단계

To a stirred solution of 6-chloro-3-(2-fluorophenyl)-7-(trimethylsilyl)-1,2,4-triazolo[4,3-b]pyridazine (1.04 g, 3.24 mmol) in anhydrous THF (15 ml) under nitrogen was added cyclobutanone (1.21 ml, 16.2 mmol), followed by solid tetrabutylammonium difluorotriphenylstannate (0.410 g, 0.650 mmol). The flask was evaporated and refilled with nitrogen four times, then stirred at room temperature for 5.75 h. More tetrabutylammonium difluorotriphenylstannate (0.403 g, 0.639 mmol) was added and the mixture was stirred for a further 36 h. The mixture was then partitioned between dichloromethane (75 ml) and water (75 ml). The aqueous layer was extracted further with dichloromethane (2×50 ml), and the combined organic extracts were dried (Na2SO4) and evaporated in, vacuo. The residue was purified by flash chromatography (silica gel. 70-100% EtOAc/hexane) to give 0.2634 g (26%) of the title compound as a cream solid; 1H NMR (360 MHz, CDCl3) δ1.81 (1H, m), 2.27 (1H, m), 2.52 (2H, m), 2.72 (2H, m), 2.87 (1H, s), 7.30 (1H, t, J=9.3 Hz), 7.36 (1H, t, J=7.5 Hz), 7.58 (1H, m), 7.88 (1H, td, J=7.3 and 1.8 Hz), 8.12 (1H, s); MS (ES+) m/e 319/321 [MH]+, 249.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06579875B1
출처 데이터셋uspto-grants-2003_06
ORD IDord-919582391af54c99846fe6dfd078cb24
출처 메모uspto-grants-2003_06