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HRID 352519作成日:2026年10月26日

3,5-Di-tert-butyl-4-hydroxybenzoyl chloride → N1-[2-(4-amino-2-butyl 1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)ethyl]-3,5-di-(1,1-dimethylethyl)-4-hydroxybenzamide

https://huagongshe.com/reaction/352519

反応式

関与物質

役割名称HCID仕込み量
反応物3,5-Di-tert-butyl-4-hydroxybenzoyl chlorideHCID 3787187—
反応物2-(4-amino-2-butyl-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)ethaneamineHCID 21946027—
生成物N1-[2-(4-amino-2-butyl 1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)ethyl]-3,5-di-(1,1-dimethylethyl)-4-hydroxybenzamideHCID 1211219156.9%

反応手順

Using the general method of Example 92, 3,5-di-(1,1dimethylethyl)-4-hydroxybenzoyl chloride (0.47 g, 1.7 mmol) was reacted with 2-(4-amino-2-butyl-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)ethaneamine (0.5 g, 1.7 mmol) to provide 0.5 g of N1-[2-(4-amino-2-butyl-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)ethyl]-3,5-di-(1,1-dimethylethyl)-4-hydroxybenzamide as a white powder, m.p. 248-250° C. Analysis: Calculated for C30H40N6O2: %C, 69.74; %H, 7.80; %N, 16.27; Found: %C, 69.65%H, 7.69; %N, 16.42. HRMS (EI) calcd for C30H40N6O2 (M+) 516.3212 found 516.3226

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06747040B2
出典データセットuspto-grants-2004_06
ORD IDord-5825175c35c7418a86ba957ca90a464b
出典メモuspto-grants-2004_06