돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1814113생성일: 2026년 10월 25일

Water → 6-(1-Benzenesulfonyl-5-methylthio-1h-pyrrolo[2,3-b]pyridin-2-yl)nicotinic acid ethyl ester

https://huagongshe.com/reaction/1814113

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Potassium AcetateHCID 517044—
반응물2-Benzenesulfonylamino-3-iodo-5-methylthiopyridineHCID 15486851—
반응물5-Ethoxycarbonyl-2-trimethylsilylethynylpyridineHCID 22504397—
용매1,4-DioxaneHCID 31275—
생성물6-(1-Benzenesulfonyl-5-methylthio-1h-pyrrolo[2,3-b]pyridin-2-yl)nicotinic acid ethyl esterHCID 6844473998.5%

반응 조건

온도100 °C

반응 단계

To a solution of 2-benzenesulfonylamino-5-methylthio-3-iodo-pyridine (100 mg) in 1,4-dioxane (2.5 ml), 5-ethoxycarbonyl-2-trimethylsilylethynylpyridine (185 mg), bistriphenylphosphine palladium dichloride (9 mg), cuprous iodide (5 mg) and potassium acetate (37 mg) were added successively and the mixture was stirred in a sealed tube at 100° C. for 15 hours. After cooling, the reaction solution was poured into water, extracted with ethyl acetate, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The resulting residue was separated using silica gel preparative thin-layer chromatography (hexane:ethyl acetate=2:1) to obtain 110 mg of the desired product as an orange oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06875770B2
출처 데이터셋uspto-grants-2005_04
ORD IDord-0f1fd7e7c0f54fbc91234c3ff00dc5b1
출처 메모uspto-grants-2005_04