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HRID 1361636作成日:2026年10月26日

N-methyl-4-(2-(4-nitrophenoxy)phenyl)pyrimidin-2-amine → 4-(2-(4-aminophenoxy)phenyl)-N-methylpyrimidin-2-amine

https://huagongshe.com/reaction/1361636

反応式

関与物質

役割名称HCID仕込み量
反応物N-methyl-4-(2-(4-nitrophenoxy)phenyl)pyrimidin-2-amineHCID 66970416—
反応物HCID 178418361HCID 178418361—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
生成物4-(2-(4-aminophenoxy)phenyl)-N-methylpyrimidin-2-amineHCID 58588498—

反応手順

To N-methyl-4-(2-(4-nitrophenoxy)phenyl)pyrimidin-2-amine (0.667 g, 2.1 mmol) and palladium, 10 wt. % on activated carbon, wet (0.44 g, 0.41 mmol) in a 100 mL round bottom flask was added MeOH under nitrogen via syringe. The atmosphere was replaced with hydrogen from a balloon and the mixture stirred rapidly for 24 h. The reaction was flushed with nitrogen, and filtered through celite rinsing with 100 mL MeOH. The filtrate was concentrated in vacuo to give 4-(2-(4-aminophenoxy)phenyl)-N-methylpyrimidin-2-amine as a light yellow solid. MS m/z=293 [M+1]+. Calc'd for C17H16N4O: 292.34.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07880000B2
出典データセットuspto-grants-2011_02
ORD IDord-7b38a7b5515d49448c887e47fca30afa
出典メモuspto-grants-2011_02