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HRID 2423316作成日:2026年10月23日

Hydrochloric Acid → 2-(3-Methoxy-4-(5-nitroquinolin-6-yloxy)phenyl)acetic acid

https://huagongshe.com/ja/reaction/2423316

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Homovanillic AcidHCID 1738—
反応物Cesium carbonateHCID 10796—
反応物6-Chloro-5-nitroquinolineHCID 4070800—
溶媒Dimethyl SulfoxideHCID 679—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物2-(3-Methoxy-4-(5-nitroquinolin-6-yloxy)phenyl)acetic acidHCID 59864834—

反応条件

温度80 °C

反応手順

Cs2CO3 (15.5 g, 47.5 mmol) was added to (24.1) (3 g, 14.4 mmol) and 3-methoxy-4-hydroxyphenylacetic acid (2.63 g, 14.4 mmol) in DMSO (30 mL) at room temperature. The mixture was then stirred at 80° C. for 4 h. After cooling, the reaction mixture was treated with water (50 mL), 3N HCl (35 mL) and EtOAc (100 mL). The product was insoluble in EtOAc, but stayed in the organic layer. So the organic layer was washed with water 4 times to get rid of all the salts, and the organic layer was separated, concentrated and dried under vacuum to afford 24.2. MS ESI (pos.) m/z: 355.1 (M+H). 1H NMR (DMSO-d6) δ 8.99 (dd, 1H); 8.24 (m, 2H); 7.77 (dd, 1H); 7.29 (d, 1H); 7.21 (d, 1H); 7.18 (d, 1H); 6.96 (dd, 1H); 3.73 (s, 3H); 3.65 (s, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07960567B2
出典データセットuspto-grants-2011_06
ORD IDord-16d0c3b2ffd34074ae81e23fc3d08fa6
出典メモuspto-grants-2011_06