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HRID 550412作成日:2026年10月25日

3-Methyl-4-[(3-fluorobenzyl)oxy]aniline → 2-{[4-({4-[(3-fluorobenzyl)oxy]-3-methylphenyl}amino)-1H-pyrazolo[3,4-d]pyrimidin-3-yl]oxy}ethanol

https://huagongshe.com/reaction/550412

反応式

関与物質

役割名称HCID仕込み量
反応物3-Methyl-4-[(3-fluorobenzyl)oxy]anilineHCID 22137933—
反応物N'-[4-cyano-3-(2-hydroxyethoxy)-1H-pyrazol-5-yl]-N,N-dimethylimidoformamideHCID 67020529—
生成物2-{[4-({4-[(3-fluorobenzyl)oxy]-3-methylphenyl}amino)-1H-pyrazolo[3,4-d]pyrimidin-3-yl]oxy}ethanolHCID 1156057058%

反応手順

The procedure described in Example 1 was repeated using N′-[4-cyano-3-(2-hydroxyethoxy)-1H-pyrazol-5-yl]-N,N-dimethylimidoformamide (2.0 g, 8.96 mmol) and 3-methyl-4-[(3-fluorobenzyl)oxy]aniline (2.5 g, 10.8 mmol) to give the title compound as a white solid (2.12 g, 58%); NMR Spectrum: 2.24 (s, 3H), 3.79 (s, 2H), 4.30 (t, 2H), 5.17 (s, 2H), 7.02 (d, 1H), 7.15 (td, 1H), 7.31 (m, 2H), 7.42 (m, 3H), 7.85 (t, 1H), 8.23 (s, 1H), 8.21 (s, 1H), 8.33 (s, 1H); Mass Spectrum: 410 (MH+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07947676B2
出典データセットuspto-grants-2011_05
ORD IDord-60408b2cef454b399c44eb2ef9fc24a8
出典メモuspto-grants-2011_05