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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1058739생성일: 2026년 10월 23일

3,5-Dimethylisoxazole-4-carboxylic acid → N-[2-(4-amino-2-butyl-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)ethyl]-3,5-dimethyl-4-isoxazolecarboxamide

https://huagongshe.com/ko/reaction/1058739

반응식

참여 물질

역할이름HCID투입량
반응물3,5-Dimethylisoxazole-4-carboxylic acidHCID 75636—
반응물2-(4-amino-2-butyl-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)ethaneamineHCID 21946027—
생성물N-[2-(4-amino-2-butyl-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)ethyl]-3,5-dimethyl-4-isoxazolecarboxamideHCID 1211219433.2%

반응 단계

Using the general method of Example 97 3,5-dimethylisoxazole-4-carboxylic acid (0.25 g, 1.7 mmole) 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 0.23 g of N-[2-(4-amino-2-butyl-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)ethyl]-3,5-dimethyl-4-isoxazolecarboxamide as a white powder, m.p. 188-189° C. Analysis: Calculated for C21H25N7O2: %C, 61.90; %H, 6.18; %N, 24.06; Found: %C, 61.92; %H, 6.15; %N, 24.28. HRMS (EI) calcd for C21H25N7O2 (M+) 407.2069 found 407.2068

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06518280B2
출처 데이터셋uspto-grants-2003_02
ORD IDord-4ac8c99feb6d405baf0eafa20236491f
출처 메모uspto-grants-2003_02