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HRID 550410作成日:2026年10月26日

3-Chloro-4-(3-fluorobenzyloxy)aniline → 2-{[4-({3-chloro-4-[(3-fluorobenzyl)oxy]phenyl}amino)-1H-pyrazolo[3,4-d]pyrimidin-3-yl]oxy}ethanol

https://huagongshe.com/reaction/550410

反応式

関与物質

役割名称HCID仕込み量
反応物3-Chloro-4-(3-fluorobenzyloxy)anilineHCID 7059263—
反応物N'-[4-cyano-3-(2-hydroxyethoxy)-1H-pyrazol-5-yl]-N,N-dimethylimidoformamideHCID 67020529—
溶媒Acetic AcidHCID 176—
溶媒Diethyl EtherHCID 3283—
生成物2-{[4-({3-chloro-4-[(3-fluorobenzyl)oxy]phenyl}amino)-1H-pyrazolo[3,4-d]pyrimidin-3-yl]oxy}ethanolHCID 1164054770.1%

反応条件

温度150 °C

反応手順

A suspension of N′-[4-cyano-3-(2-hydroxyethoxy)-1H-pyrazol-5-yl]-N,N-dimethylimidoformamide (500 mg, 2.24 mmol) and 3-chloro-4-[(3-fluorobenzyl)oxy]aniline (564 mg, 2.24 mmol) in acetic acid (2.5 ml) was heated under microwave at 150° C. for 2 minutes. The crude mixture was diluted with diethyl ether and the precipitated solid was filtered, rinsed with ether and dried under vacuum to give the title compound as a white solid (675 mg, 70%); NMR spectrum: 3.79 (t, 2H), 4.31 (t, 2H), 5.26 (s, 2H), 7.18 (t, 1H), 7.25 (d, 1H), 7.29-7.33 (m, 2H), 7.44-7.49 (m, 1H), 7.57 (d, 1H), 7.87 (s, 1H), 8.27 (s, 1H), 8.47 (s, 1H); Mass Spectrum: 430 (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-566ccc9e3e00450db0e603db7e323081
出典メモuspto-grants-2011_05