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HRID 2044934作成日:2026年10月25日

1-Butanol → N-((2-(3-fluoro-phenyl)-8-methoxyquinolin-3-yl)methyl)-9H-purin-6-amine

https://huagongshe.com/reaction/2044934

反応式

関与物質

役割名称HCID仕込み量
反応物1-ButanolHCID 263—
反応物DiisopropylethylamineHCID 81531—
反応物Purine, 6-bromo-HCID 5287830—
反応物(2-(3-Fluorophenyl)-8-methoxyquinolin-3-yl)methanamineHCID 57707903—
溶媒Ethyl AcetateHCID 8857—
生成物N-((2-(3-fluoro-phenyl)-8-methoxyquinolin-3-yl)methyl)-9H-purin-6-amineHCID 178488602—

反応条件

温度100 °C

反応手順

A mixture of 6-bromopurine (0.1418 g, 0.7125 mmol), (2-(3-fluorophenyl)-8-methoxyquinolin-3-yl)methanamine (0.2213 g, 0.7838 mmol), and N,N-diiso-propylethylamine (0.2482 mL, 1.425 mmol) in 1-butanol (7.125 mL, 0.7125 mmol) was stirred at 100° C. After 24 h, the mixture was removed from the heat and concentrated under reduced pressure. The residue was purified by flash column chromatography on a silica gel column using 50% of CH2Cl2:MeOH:NH4OH (89:9:1) in CH2Cl2 as eluent to give an off-white solid. The off-white solid was suspended in EtOAc and filtered to give N-((2-(3-fluoro-phenyl)-8-methoxyquinolin-3-yl)methyl)-9H-purin-6-amine as a white solid: 1H NMR (400 MHz, DMSO-d6) δ ppm 12.95 (1 H, s), 8.18-8.30 (2 H, m), 8.11 (2 H, s), 7.42-7.61 (5 H, m), 7.28-7.36 (1 H, m), 7.16 (1 H, dd, J=7.1, 1.7 Hz), 4.71-4.95 (2 H, m), 3.95 (3 H, s); LC-MS (ESI) m/z 401.2 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08586739B2
出典データセットuspto-grants-2013_11
ORD IDord-8ed7d558f674488fac037b01f3a82c76
出典メモuspto-grants-2013_11