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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 353856생성일: 2026년 10월 25일

Quinoline-3-carbonyl Chloride → N3-[4-(4-amino-1H-imidazo[4,5-c]quinolin-1-yl)butyl]-3-quinolinecarboxamide

https://huagongshe.com/reaction/353856

반응식

참여 물질

역할이름HCID투입량
반응물Quinoline-3-carbonyl ChlorideHCID 11030631—
반응물1-(4-aminobutyl)-1H-imidazo[4,5-c]quinolin-4-amineHCID 15453775—
생성물N3-[4-(4-amino-1H-imidazo[4,5-c]quinolin-1-yl)butyl]-3-quinolinecarboxamideHCID 9909494—

반응 단계

According to the general method of Example 14, 1-(4-aminobutyl)-1H-imidazo[4,5-c]quinolin-4-amine and quinoline-3-carbonyl chloride were combined to provide N3-[4-(4-amino-1H-imidazo[4,5-c]quinolin-1-yl)butyl]-3-quinolinecarboxamide as a white crystalline solid, m.p. 116.0-118.0° C. (decomposition). 1H NMR (300 MHz, DMSO-d6) δ 9.24 (d, J=2.1 Hz, 1H), 8.86 (t, J=5.1 Hz, 1H), 8.74 (d, J=2.1 Hz, 1H), 8.25 (s, 1H), 8.09-8.05 (m, 3H), 7.86 (dt, J=7.5, 1.0 Hz, 1H), 7.69 (t, J=7.5 Hz, 1H), 7.61 (d, J=7.5 Hz, 1H), 7.40 (t, J=7.5 Hz, 1H), 7.21 (t, J=7.5 Hz, 1H), 6.68 (s, 2H), 4.67 (t, J=6.9 Hz, 2H), 1.97 (quintet, J=7.2 Hz, 2H), 1.65 (quintet, J=7.2 Hz, 2H); MS (EI) m/e 410.1864 (410.1855 calcd for C24H22N6O).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06756382B2
출처 데이터셋uspto-grants-2004_06
ORD IDord-bb170a59cb5444b68801adda80bbc036
출처 메모uspto-grants-2004_06