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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 598474생성일: 2026년 10월 24일

4-Aminophenol → 4-(4-aminophenoxy)-N,N-dimethylpyridine-2-carboxamide

https://huagongshe.com/ko/reaction/598474

반응식

참여 물질

역할이름HCID투입량
반응물4-AminophenolHCID 403—
반응물DimethylamineHCID 674—
반응물4-chloro-N,N-dimethylpyridine-2-carboxamideHCID 4962252—
반응물4-chloropyridine-2-carbonyl ChlorideHCID 11095146—
생성물4-(4-aminophenoxy)-N,N-dimethylpyridine-2-carboxamideHCID 23614563—

반응 단계

Entry 24; 4-Chloropyridine-2-carbonyl chloride was reacted with dimethylamine according to Method A2, Step 3b. The resulting 4-chloro-N,N-dimethyl-2-pyridinecarboxamide was reacted with 4-aminophenol according to Method A2, Step 4 to give 4-(2-(N,N-dimethylcarbamoyl)-4-pyridyloxy)aniline. 5-(Trifluoromethyl)-2-methoxyaniline was converted into 5-(trifluoromethyl)-2-methoxyphenyl isocyanate according to Method B1. 5-(Trifluoromethyl)-2-methoxyphenyl isocyanate was reacted with 4-(2-(N,N-dimethylcarbamoyl)-4-pyridyloxy) an line according to Method C1a to afford the urea.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07897623B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-c2a4d9ae63384325a095aaee73a3f8a9
출처 메모uspto-grants-2011_03