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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1887033생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1887033

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물TriphenylphosphineHCID 11776—
반응물1,2-Dibromo-1,1,2,2-tetrachloroethaneHCID 69426—
반응물N'-(6-Chloro-5-(trimethylsilyl)pyridazin-3-yl)-2-fluorobenzohydrazideHCID 15486174—
용매AcetonitrileHCID 6342—
용매DichloromethaneHCID 6344—
생성물6-Chloro-3-(2-fluorophenyl)-7-(trimethylsilyl)-[1,2,4]triazolo[4,3-b]pyridazineHCID 1548617597.9%

반응 단계

Compound 22 (4.1 g, 12.1 mmol) and 1,2-dibromotetrachloroethane (7.9 g, 24.2 mmol) were suspended in acetonitrile (80 mL) and cooled to less than 5° C. Triphenylphosphine (11 g, 30.2 mmol) was added in small portions allowing the reaction to exotherm slightly but keeping the temperature at about 5-7° C. The solids started to dissolve and then a new precipitate began to form. The thick mixture was stirred cold for 15 min. Triethylamine (10 mL, 72.6 mmol) was added dropwise, again allowing an exotherm but keeping the temperature about 5-7° C. The reaction was stirred in an ice-water bath for 1 hr. The mixture was diluted with dichloromethane (200 mL) and washed with water. The organic layer was dried over Na2SO4 and concentrated to a brown liquid. The material was combined with crude material from another (2.9 mmol) reaction and purified on an Analogix automated column chromatography system (SF25-80 g column, 10-40% EtOAc/heptane) to provide 3.8 g (79%) of 23 as a tan, slightly sticky, solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08501738B2
출처 데이터셋uspto-grants-2013_08
ORD IDord-7ab90d09e8164061a4920c572c0504ec
출처 메모uspto-grants-2013_08