돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 533616생성일: 2026년 10월 26일

1,4-Dioxane → 2-(2-ethylsulfanylphenyl)-6-(2-fluorophenyl)-3-methyl-3H-imidazo[4,5-b]pyridine

https://huagongshe.com/reaction/533616

반응식

참여 물질

역할이름HCID투입량
반응물1,4-DioxaneHCID 31275—
반응물Potassium Phosphate, TribasicHCID 62657—
반응물2-Fluorophenylboronic acidHCID 2734354—
반응물6-bromo-2-(2-ethylsulfanylphenyl)-3-methyl-3H-imidazo[4,5-b]pyridineHCID 67982033—
촉매2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
용매WaterHCID 962—
생성물2-(2-ethylsulfanylphenyl)-6-(2-fluorophenyl)-3-methyl-3H-imidazo[4,5-b]pyridineHCID 8670821195.5%

반응 조건

온도80 °C

반응 단계

To a mixture of 6-bromo-2-(2-ethylsulfanylphenyl)-3-methyl-3H-imidazo[4,5-b]pyridine (350 mg) and 1,4-dioxane (5 ml), 2-fluorophenylboronic acid (150 mg), tripotassium phosphate (600 mg), 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl (25 mg), and tris(dibenzylideneacetone)palladium(0) (14 mg) were sequentially added, heated to 80° C., and stirred with heating for 8 hours. The reaction mixture was cooled to room temperature, and then water was poured into the reaction mixture, and extracted with ethyl acetate. The organic layer was dried over sodium sulfate, and concentrated under reduced pressure. The resulting residue was subjected to silica gel column chromatography to give 349 mg of 2-(2-ethylsulfanylphenyl)-6-(2-fluorophenyl)-3-methyl-3H-imidazo[4,5-b]pyridine (hereinafter referred to as Present Compound 58).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08853238B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-589266803c1c47e9a06236c2337414e4
출처 메모uspto-grants-2014_10