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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 746531생성일: 2026년 10월 24일

1-Naphthalenecarbonyl chloride, 2-ethoxy- → N1-[4-(4-amino-1H-imidazo[4,5-c]quinolin-1-yl)butyl]-2-ethoxy-1-naphthamide

https://huagongshe.com/ko/reaction/746531

반응식

참여 물질

역할이름HCID투입량
반응물1-Naphthalenecarbonyl chloride, 2-ethoxy-HCID 108679—
반응물1-(4-aminobutyl)-1H-imidazo[4,5-c]quinolin-4-amineHCID 15453775—
생성물N1-[4-(4-amino-1H-imidazo[4,5-c]quinolin-1-yl)butyl]-2-ethoxy-1-naphthamideHCID 12144524—

반응 단계

According to the general method of Example 14, 1-(4-aminobutyl)-1H-imidazo[4,5-c]quinolin-4-amine and 2-ethoxy-1-naphthoyl chloride were combined to provide N1-[4-(4-amino-1H-imidazo[4,5-c]quinolin-1-yl)butyl]-2-ethoxy-1-naphthamide as a white powder, m.p. 219° C. (decomposition). 1H NMR (300 MHz, DMSO-d6) δ 8.33 (t, J=5.8 Hz, 1H), 8.22 (s, 1H), 8.09 (d, J=8.0 Hz, 1H), 7.91 (d, J=8.7 Hz, 11H), 7.87-7.84 (m, 1H), 7.64-7.56 (m, 2H), 7.47-7.22 (m, 5H), 6.60 (s, 2H), 4.69 (t, J=7.2 Hz, 2H), 4.09 (q, J=7.2 Hz, 2H), 3.37 (m, 2H), 2.01 (m, 2H), 1.64 (m, 2H), 1.18 (t, J=7.2 Hz, 3H); MS (EI) m/e 453.2157 (453.2165 calcd for C27H27N5O2).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07393859B2
출처 데이터셋uspto-grants-2008_07
ORD IDord-f923c313d5ab4c54a11c0be05a8c7b32
출처 메모uspto-grants-2008_07