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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1369437생성일: 2026년 10월 26일

1,2-Dibromo-1,1,2,2-tetrafluoroethane → 7-Bromo-6-chloro-3-(2-fluorophenyl)-1,2,4-triazolo[4,3-b]pyridazine

https://huagongshe.com/reaction/1369437

반응식

참여 물질

역할이름HCID투입량
반응물1,2-Dibromo-1,1,2,2-tetrafluoroethaneHCID 31301—
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—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물7-Bromo-6-chloro-3-(2-fluorophenyl)-1,2,4-triazolo[4,3-b]pyridazineHCID 1548617688%

반응 단계

Tetrabutylammonium difluorotriphenylstannate (6.8 g, 10.8 mmol) was added to a suspension of 6-chloro-3-(2-fluorophenyl)-7-(trimethylsilyl)-1,2,4-triazolo[4,3-b]pyridazine (3.17 g, 9.88 mmol), prepared as in Example 25 Step c), and 1,2-dibromotetrafluoroethane (6.0 ml, 50 mmol) in anhydrous THF (75 ml) and the mixture was stirred at room temperature under nitrogen for 18 h. The mixture was diluted with dichloromethane (100 ml), filtered and the filtrate was concentrated. Flash column chromatography on silica gel, eluting with 50-100% EtOAc-hexane, gave 7-bromo-6-chloro-3-(2-fluorophenyl)-1,2,4-triazolo[4,3-b]pyridazine (2.84 g, 88%) as an off-white solid; 1H NMR (360 MHz, CDCl3) δ7.31 (1H, dd, J=10 and 10 Hz), 7.36 (1H, ddd, J=8, 8 and 1 Hz), 7.57-7.63 (1H, m), 7.87 (1H, ddd, J=7, 7 and 2 Hz), 8.49 (1H, s); MS (ES+) m/e 327/329/331 [MH]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06579875B1
출처 데이터셋uspto-grants-2003_06
ORD IDord-bfe563adb7d34089ba47ecc4ceee669c
출처 메모uspto-grants-2003_06