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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1275017생성일: 2026년 10월 26일

Triethylamine → N-[4-Chloro-3-(4-methylpiperazin-1-yl)phenyl]-N'-[4-(pyridin-4-yl)naphth-1-yl]urea

https://huagongshe.com/reaction/1275017

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물TriphosgeneHCID 94429—
반응물4-(Pyridin-4-yl)naphth-1-ylamineHCID 10857012—
반응물4-Chloro-3-(4-methylpiperazin-1-yl)anilineHCID 18180073—
용매DichloromethaneHCID 6344—
생성물N-[4-Chloro-3-(4-methylpiperazin-1-yl)phenyl]-N'-[4-(pyridin-4-yl)naphth-1-yl]ureaHCID 22118919—

반응 단계

To a stirred solution of triphosgene (39 mg, 0.13 mmole) in dichloromethane (10 ml) was added a solution of 4-(pyridin-4-yl)naphth-1-ylamine (D1, 82 mg, 0.37 mmole) and triethylamine (0.05 ml, 0.37 mmole) dropwise over 30 minutes. When the addition was complete the mixture was stirred at room temperature for 15 minutes, then a solution of 4-chloro-3-(4-methylpiperazin-1-yl)aniline (100 mg, 0.44 mmole, EP0533268A1) in dichloromethane (10 ml) was added over 5 minutes. After 18 h, the mixture was washed with 10% aqueous sodium carbonate solution and water, dried (Na2SO4) and evaporated to dryness. The residue was purified by column chromatography on silica gel eluting with 10% methanol/dichloromethane and the title compound was obtained as a white solid on trituration with ether (47 mg, 27%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06159979
출처 데이터셋uspto-grants-2000_12
ORD IDord-58d818f6374b4e928a506fea67f2417a
출처 메모uspto-grants-2000_12