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HRID 78382作成日:2026年10月25日

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

https://huagongshe.com/reaction/78382

反応式

関与物質

役割名称HCID仕込み量
反応物4-AminophenolHCID 403—
反応物DimethylamineHCID 674—
反応物4-chloro-N,N-dimethylpyridine-2-carboxamideHCID 4962252—
反応物4-chloropyridine-2-carbonyl ChlorideHCID 11095146—
生成物4-(4-aminophenoxy)-N,N-dimethylpyridine-2-carboxamideHCID 23614563—

反応手順

Entry 100: 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. 4-Chloro-2-methoxy-5-(trifluoromethyl)aniline was synthesized according to Method A7. 4-Chloro-2-methoxy-5-(trifluoromethyl)aniline was converted into 4-chloro-2-methoxy-5-(trifluoromethyl)phenyl isocyanate according to Method B1. According to Method C1a, 4-chloro-2-methoxy-5-(trifluoromethyl)phenyl isocyanate was reacted with 4-(2-(N,N-dimethylcarbamoyl)-4-pyridyloxy)aniline to afford the urea.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08841330B2
出典データセットuspto-grants-2014_09
ORD IDord-0469a9e2f5a4441b9c393a8e749ad04c
出典メモuspto-grants-2014_09