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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1473934생성일: 2026년 10월 25일

Ammonia → 2-(3-ethylsulfanyl-pyridin-2-yl)-1-methyl-5-pentafluoroethyl-1H-benzimidazole

https://huagongshe.com/reaction/1473934

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물Sodium BicarbonateHCID 516892—
반응물Sodium pentafluoropropionateHCID 2733305—
반응물2-(3-ethylsulfanyl-pyridin-2-yl)-5-iodo-1-methyl-1H-benzimidazoleHCID 71247076—
촉매Copper iodideHCID 83717—
용매O-XyleneHCID 7237—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물2-(3-ethylsulfanyl-pyridin-2-yl)-1-methyl-5-pentafluoroethyl-1H-benzimidazoleHCID 8672517772%

반응 조건

온도160 °C

반응 단계

A mixture of 2-(3-ethylsulfanyl-pyridin-2-yl)-5-iodo-1-methyl-1H-benzimidazole (340 mg), copper iodide (410 mg), sodium pentafluoropropionate (800 mg), NMP (5 ml), and xylene (5 ml) was stirred at 160° C. for 5 hours. The reaction mixture was allowed to cool to room temperature, and then saturated aqueous sodium hydrogen carbonate solution and 28% ammonia solution were poured thereto. Then, the mixture was extracted with t-butylmethyl ether. The organic layer was dried over sodium sulfate, and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to give 2-(3-ethylsulfanyl-pyridin-2-yl)-1-methyl-5-pentafluoroethyl-1H-benzimidazole (240 mg), which is hereinafter referred to as “the present compound 26”.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09018134B2
출처 데이터셋uspto-grants-2015_04
ORD IDord-e5544fa675e64912806e761787cc465b
출처 메모uspto-grants-2015_04