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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 533615생성일: 2026년 10월 26일

Ammonium Chloride → 2-(2-ethylsulfanylphenyl)-3-methyl-6-phenyl-3H-imidazo[4,5-b]pyridine

https://huagongshe.com/reaction/533615

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물Potassium Phosphate, TribasicHCID 62657—
반응물Phenylboronic AcidHCID 66827—
반응물6-bromo-2-(2-ethylsulfanylphenyl)-3-methyl-3H-imidazo[4,5-b]pyridineHCID 67982033—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
촉매2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
용매1,4-DioxaneHCID 31275—
생성물2-(2-ethylsulfanylphenyl)-3-methyl-6-phenyl-3H-imidazo[4,5-b]pyridineHCID 86708210106.6%

반응 조건

온도70 °C

반응 단계

A mixture of 6-bromo-2-(2-ethylsulfanylphenyl)-3-methyl-3H-imidazo[4,5-b]pyridine (0.35 g), tripotassium phosphate (0.42 g), phenylboronic acid (0.13 g), 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl (0.03 g), tris(dibenzylideneacetone)dipalladium(0) (0.01 g), and 1,4-dioxane (3 ml) was stirred with heating at 70° C. for 2 hours, and then heated to 90° C., and stirred with heating for further 2 hours. Into the reaction mixture cooled to room temperature, saturated aqueous ammonium chloride solution was poured, 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 0.37 g of 2-(2-ethylsulfanylphenyl)-3-methyl-6-phenyl-3H-imidazo[4,5-b]pyridine (hereinafter referred to as Present Compound 56).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08853238B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-c7c9d95500ee46b18d8f89061085efdd
출처 메모uspto-grants-2014_10