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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 346644생성일: 2026년 10월 25일

Cyclohexylamine → 3-Quinolinecarboxamide, 1,2-dihydro-N-cyclohexyl-4-hydroxy-2-oxo-

https://huagongshe.com/reaction/346644

반응식

참여 물질

역할이름HCID투입량
반응물CyclohexylamineHCID 7965—
반응물Ethyl 4-hydroxy-2-oxo-1,2-dihydroquinoline-3-carboxylateHCID 54684458—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물3-Quinolinecarboxamide, 1,2-dihydro-N-cyclohexyl-4-hydroxy-2-oxo-HCID 5468010587.2%

반응 단계

Cyclohexylamine (13.88 mL, 121.33 mmol) was added to a solution of Compound 112 (9.4 g, 40.44 mmol) in toluene (200 mL) and refluxed for 4 h. The solution was cooled and the solvent was evaporated under vacuum. The residue obtained was suspended in water, briefly sonicated, and filtered. The crude product was recrystallized by ether to yield 10.1 g (87%) of white solids. M.P. 223° C. 1H NMR (DMSO-d6): δ 1.3 (m, 4H), 1.6 (m, 2H), 1.7 (m, 2H), 1.9 (m, 2H), 3.8 (m, 1H), 7.25 (t, J=7.7 Hz, 1H), 7.35 (d, J=8.3 Hz, 1H), 7.65 (t, J=7.2 Hz, 1H), 7.95 (d, J=7.7 Hz, 1H), 10.44 (b, 1H); EIMS (neg. mode): 285 (M−H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07173036B2
출처 데이터셋uspto-grants-2007_02
ORD IDord-67364dec13c94297b5be354191005dda
출처 메모uspto-grants-2007_02