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HRID 23532생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/23532

반응식

참여 물질

역할이름HCID투입량
반응물TrimethylamineHCID 1146—
반응물4-((2-Chloropyrimidin-4-yl)oxy)naphthalen-1-amineHCID 22573839—
촉매Tetraethylammonium cyanideHCID 3014735—
용매DimethylformamideHCID 6228—
생성물4-(4-Amino-naphthalen-1-yloxy)-pyrimidine-2-carbonitrileHCID 2257383354.1%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06852717B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-eb0d84ff5d9f4db9b3d85b4257abc054
출처 메모uspto-grants-2005_02