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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 353871생성일: 2026년 10월 24일

Isoquinoline-1-carboxylic acid → N1-{4-[4-amino-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-1-yl]butyl}-1-isoquinolinecarboxamide

https://huagongshe.com/ko/reaction/353871

반응식

참여 물질

역할이름HCID투입량
반응물Isoquinoline-1-carboxylic acidHCID 68092—
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}-1-isoquinolinecarboxamideHCID 23512699—

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 isoquinoline-1-carboxylic acid were combined to provide N1-{4-[4-amino-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-1-yl]butyl}-1-isoquinolinecarboxamide as a yellow crystalline solid, m.p. 61.0-63.0° C. 1H NMR (300 MHz, DMSO-d6) δ 8.94 (t, J=5.9 Hz, 1H), 8.87 (d, J=8.5 Hz, 1H), 8.51 (d, J=5.6 Hz, 1H), 8.05-7.96 (m, 3H), 7.84-7.96 (m, 1H), 7.70-7.65 (m, 1H), 7.61 (dd, J=8.3, 1.1 Hz, 1H), 7.37 (dt, J=7.7, 1.0 Hz, 1H), 7.19 (dt, J=7.6, 1.2 Hz, 1H), 6.53 (broad s, 2H), 4.60 (t, J=7.2 Hz, 2H), 3.81 (t, J=6.7 Hz, 2H), 3.41 (m, 2H), 3.28-3.12 (m, 5H), 1.92-1.76 (m, 4H); MS (EI) m/e 468.2261 (468.2274 calcd for C27H28N6O2).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06756382B2
출처 데이터셋uspto-grants-2004_06
ORD IDord-2edbeb7e1e674317a3de77b69f9df8bd
출처 메모uspto-grants-2004_06