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HRID 33917作成日:2026年10月25日

2-(Chloromethyl)quinoline → 2-((4-(5-(Pyridin-4-yl)oxazol-4-yl)phenoxy)methyl)quinoline

https://huagongshe.com/reaction/33917

反応式

関与物質

役割名称HCID仕込み量
反応物2-(Chloromethyl)quinolineHCID 20394—
反応物Cesium fluorideHCID 25953—
反応物4-(5-(Pyridin-4-yl)oxazol-4-yl)phenolHCID 135988007—
溶媒DimethylformamideHCID 6228—
生成物2-((4-(5-(Pyridin-4-yl)oxazol-4-yl)phenoxy)methyl)quinolineHCID 1160330220.1%

反応条件

温度80 °C

反応手順

To a solution of compound 4-(5-(pyridin4-yl)oxazol4-yl)phenol (90 mg, 0.38 mmol) in 1 mL of dry DMF was added CsF (115 mg, 0.76 mmol). After stirring for 0.5 h, 2-(chloromethyl)quinoline (67 mg, 0.38 mmol) was added and the reaction was heated at 80° C. for 48 h. Upon removal of DMF under vacuum, the residue was purified by PTLC (1:2 hexane/EtOAc) to give 29 mg (20%) of the title compound as a white solid. 1H NMR (400 MHz, CDCl3) δ: 5.47 (s, 2H), 7.11 (m, 2H), 7.56 (m, 5H), 7.70 (d, 1H), 7.78 (t, 1H), 7.86 (d, 1H), 8.01 (s, 1H), 8.12 (d, 1H), 8.26 (d, 1H), 8.57 (d, (2H). MS m/z: 380 [M+1]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07429665B2
出典データセットuspto-grants-2008_09
ORD IDord-d986365884614a968ab7c5004a05b7d6
出典メモuspto-grants-2008_09