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HRID 346644作成日:2026年10月26日

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

https://huagongshe.com/reaction/346644

反応式

関与物質

役割名称HCID仕込み量
反応物CyclohexylamineHCID 7965—
反応物Ethyl 4-hydroxy-2-oxo-1,2-dihydroquinoline-3-carboxylateHCID 54684458—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物3-Quinolinecarboxamide, 1,2-dihydro-N-cyclohexyl-4-hydroxy-2-oxo-HCID 5468010587.2%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07173036B2
出典データセットuspto-grants-2007_02
ORD IDord-67364dec13c94297b5be354191005dda
出典メモuspto-grants-2007_02