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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 353839생성일: 2026년 10월 23일

4-Benzoylbenzoyl chloride → HCID 12144523, 화합물

https://huagongshe.com/ko/reaction/353839

반응식

참여 물질

역할이름HCID투입량
반응물4-Benzoylbenzoyl chlorideHCID 12912141—
반응물1-(4-aminobutyl)-1H-imidazo[4,5-c]quinolin-4-amineHCID 15453775—
생성물HCID 12144523HCID 1214452316.2%

반응 단계

Using the general method of Example 14, 1-(4-aminobutyl)-1H-imidazo[4,5-c]quinolin-4-amine (0.51 g, 2.0 mmol) was reacted with 4-benzoylbenzoyl chloride (2.0 mmol) to provide 0.15 g of N1-[4-(4-amino-1H-imidazo[4,5-c]quinolin1-yl)butyl]-4-benzoylbenzamide as a white solid, m.p. 159-161° C. 1H NMR (500 MHz, CDCl3) δ8.06 (s, 1H), 7.96 (d, J=8.0 Hz, 1H), 7.91 (d, J=8.0 Hz, 1H), 7.85 (d, J=8.0 Hz, 2H), 7.81 (d, J=8.0 Hz, 2H), 7.76 (d, J=8.0 Hz, 2H), 7.60 (m, 2H), 7.49 (t, J=8.0 Hz, 2H), 7.48 (t, J=8.0 Hz, 1H), 7.24 (broad s, 1H), 6.86 (broad s, 1H), 6.60 (t, J=6 Hz, 1H), 4.69 (t, J=7.0 Hz, 2H), 3.62 (q, J=6.0 Hz, 2H), 2.14 (quintet, J=7.0 Hz, 2H), 1.82 (quintet, J=7.0 Hz, 2H); MS (EI) m/e 463.2002 (463.2008 calcd for C28H25N5O2).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06756382B2
출처 데이터셋uspto-grants-2004_06
ORD IDord-cc42dc94af2049fc9b8f098672e67287
출처 메모uspto-grants-2004_06