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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 636632생성일: 2026년 10월 24일

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/ko/reaction/636632

반응식

참여 물질

역할이름HCID투입량
반응물3,5-Di-tert-butyl-4-hydroxybenzoyl chlorideHCID 3787187—
반응물2-(4-amino-2-butyl-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)ethaneamineHCID 21946027—
생성물N1-[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%

반응 단계

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

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06194425B1
출처 데이터셋uspto-grants-2001_02
ORD IDord-d703b411bd3c4316ab10e2ee94d3bb9e
출처 메모uspto-grants-2001_02