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HRID 1876171作成日:2026年10月25日

N-Methyl-4-anisidine → (4-Methoxy-phenyl)-methyl-(2-trifluoromethyl-quinolin-4-yl)-amine

https://huagongshe.com/reaction/1876171

反応式

関与物質

役割名称HCID仕込み量
反応物N-Methyl-4-anisidineHCID 22250—
反応物4-Chloro-2-(trifluoromethyl)quinolineHCID 2736709—
溶媒Acetic AcidHCID 176—
生成物(4-Methoxy-phenyl)-methyl-(2-trifluoromethyl-quinolin-4-yl)-amineHCID 6851681370%

反応条件

温度105 °C

反応手順

A mixture of 4-chloro-2-(trifluoromethyl)quinoline 0.232 g (1.0 mmol) and 4-methoxy-N-methylaniline 0.137 g (1.0 mmol) in glacial acetic acid 3 mL was stirred at 100-110° C. for 24 h. The reaction mixture was directly subjected to gradient column chromatography (EtOAc/hexanes, 0% to 50%) to give the titled compound in 70% yield. 1H NMR (CDCl3, 400 MHz): δ 8.11-8.08 (m, 1H), 7.62-7.58 (m, 1H), 7.58-7.55 (m, 1H), 7.27-7.22 (m, 2H), 6.97 (d, 2H, J=9.0 Hz), 6.84 (d, 2H, J=9.0 Hz), 3.79 (s, 3H), 3.49 (s, 3H). m/z: 333.2 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08309562B2
出典データセットuspto-grants-2012_11
ORD IDord-912bc5ab8f1945ac86e34b93be8aac07
出典メモuspto-grants-2012_11