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HRID 923750생성일: 2026년 10월 27일

Chloroform → 6-bromo-2-(2-ethylsulfonylphenyl)-3-methyl-3H-imidazo[4,5-b]pyridine

https://huagongshe.com/reaction/923750

반응식

참여 물질

역할이름HCID투입량
반응물ChloroformHCID 6212—
반응물Sodium ThiosulfateHCID 24477—
반응물m-Chloroperbenzoic acidHCID 70297—
반응물6-bromo-2-(2-ethylsulfanylphenyl)-3-methyl-3H-imidazo[4,5-b]pyridineHCID 67982033—
용매WaterHCID 962—
생성물6-bromo-2-(2-ethylsulfonylphenyl)-3-methyl-3H-imidazo[4,5-b]pyridineHCID 86708205—

반응 단계

To a mixture of 6-bromo-2-(2-ethylsulfanylphenyl)-3-methyl-3H-imidazo[4,5-b]pyridine (0.20 g) and chloroform (3 ml), 3-chloroperbenzoic acid (purity: not less than 65%) (0.34 g) was added under ice-cooling, and then heated to room temperature, and stirred for 3.5 hours. Chloroform and saturated aqueous sodium thiosulfate solution were poured thereinto under ice-cooling, and stirred, and then, water was poured, and extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium hydrogen carbonate solution and saturated brine, dried over sodium sulfate, and concentrated under reduced pressure. The resulting solid was washed with hexane, and dried to give 0.20 g of 6-bromo-2-(2-ethylsulfonylphenyl)-3-methyl-3H-imidazo[4,5-b]pyridine (hereinafter referred to as Present Compound 44).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09278983B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-5bd33a2738594874a80dad430491b8a5
출처 메모uspto-grants-2016_03