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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 746560생성일: 2026년 10월 24일

4-(1H-Pyrrol-1-yl)benzoic acid → N1-{4-[4-amino-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-1-yl]butyl}-4-(1-pyrrolyl)benzamide

https://huagongshe.com/ko/reaction/746560

반응식

참여 물질

역할이름HCID투입량
반응물4-(1H-Pyrrol-1-yl)benzoic acidHCID 2737256—
반응물1-(4-aminobutyl)-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-4-amineHCID 22180872—
생성물N1-{4-[4-amino-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-1-yl]butyl}-4-(1-pyrrolyl)benzamideHCID 23512672—

반응 단계

According to the general method of Example 50, 1-(4-aminobutyl)-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-4-amine and 4-(1-pyrrolyl)benzoic acid were combined to provide N1-{4-[4-amino-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-1-yl]butyl}-4-(1-pyrrolyl)benzamide as an off white powder, m.p. 173.0-174.9° C. 1H NMR (300 MHz, DMSO-d6) δ 8.52 (t, J=5.5 Hz, 1H), 8.02 (d, J=7.9 Hz, 1H), 7.90 (d, J=8.7 Hz, 2H), 7.67 (d, J=8.7 Hz, 2H), 7.61 (dd, J=8.4, 1.1 Hz, 1H), 7.48 (t, J=2.2 Hz, 2H), 7.39 (m, 1H), 7.19 (dt, J=7.6, 1.1 Hz, 1H), 6.53 (broad s, 2H), 6.30 (t, J=2.2 Hz, 2H), 4.57 (t, J=7.0 Hz, 2H), 3.82 (t, J=6.7 Hz, 2H), 3.33 (m, 2H), 3.26 (s, 3H), 3.20 (t, J=6.7 Hz, 2H), 1.87 (m, 2H), 1.71 (m, 2H); MS (EI) m/e 482.2421 (482.2430 calcd for C28H30N6O2).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07393859B2
출처 데이터셋uspto-grants-2008_07
ORD IDord-805b91bfc71743529ddec36660aefeab
출처 메모uspto-grants-2008_07