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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1936717생성일: 2026년 10월 25일

Triethylamine → N-[3-(1-Methylpiperdin-4-yl)indol-5-yl]-N'-[4-(pyridin-4-yl)naphth-1-yl]-urea

https://huagongshe.com/reaction/1936717

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Potassium CarbonateHCID 11430—
반응물TriphosgeneHCID 94429—
반응물4-(Pyridin-4-yl)naphth-1-ylamineHCID 10857012—
반응물3-(1-Methylpiperidin-4-yl)-1h-indol-5-amineHCID 11831220—
용매DichloromethaneHCID 6344—
생성물N-[3-(1-Methylpiperdin-4-yl)indol-5-yl]-N'-[4-(pyridin-4-yl)naphth-1-yl]-ureaHCID 9912824—

반응 단계

To a stirred solution of triphosgene (0.09 g, 0.31 mmole) in dichloromethane (15 ml) under argon, was added dropwise a solution of 4-(pyridin-4-yl)naphth-1-ylamine (D3, 0.17 g, 0.77 mmole) and triethylamine (0.12 ml, 0.83 mmole) in dichloromethane (10 ml). The mixture was then stirred at room temperature for 20 minutes, then a solution of 5-amino-3-(1-methylpiperidin-4-yl)-1H-indole (D2, 0.15 g, 0.66 mmole) in dichloromethane (10 ml) was slowly added. After stirring the mixture for 1 hour, dilute potassium carbonate solution (10 ml) was added. The precipitated solid mass was collected and purified by flash chromatography on silica gel eluting with CH2Cl2/MeOH/NH4OH (100:10:1) to afford the title compound as a buff powder (0.14 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06391891B1
출처 데이터셋uspto-grants-2002_05
ORD IDord-238f452054944339b0db327ba733cb72
출처 메모uspto-grants-2002_05