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HRID 23532作成日:2026年10月25日

Trimethylamine → 4-(4-Amino-naphthalen-1-yloxy)-pyrimidine-2-carbonitrile

https://huagongshe.com/reaction/23532

反応式

関与物質

役割名称HCID仕込み量
反応物TrimethylamineHCID 1146—
反応物4-((2-Chloropyrimidin-4-yl)oxy)naphthalen-1-amineHCID 22573839—
触媒Tetraethylammonium cyanideHCID 3014735—
溶媒DimethylformamideHCID 6228—
生成物4-(4-Amino-naphthalen-1-yloxy)-pyrimidine-2-carbonitrileHCID 2257383354.1%

反応手順

To a 0° C. solution of trimethyl amine (20% solution in water, 3.8 mmol) in 2 mL of dimethylformamide was added 4-(2-chloro-pyrimidin-4-yloxy)-naphthalen-1-ylamine (270 mg, 1 mmol). The deep tan solution was warmed to room temperature for 3 h, during which the initially light suspension became a brown suspension. After this time, tetraethylammonium cyanide (156 mg, 1 mmol) was added all at once to provide a deep amber solution. After 1 h, the reaction was quenched with water, extracted with EtOAc and dried over magnesium sulfate. Column chromatography (10-60% EtOAc-hexanes) provided 142 mg (54%) of 4-(4-amino-naphthalen-1-yloxy)-pyrimidine-2-carbonitrile.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06852717B2
出典データセットuspto-grants-2005_02
ORD IDord-eb0d84ff5d9f4db9b3d85b4257abc054
出典メモuspto-grants-2005_02