戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1178773作成日:2026年10月25日

Ethanol → (3-{[3-(2-Isopropoxy-phenoxy)-propylamino]-methyl}-phenyl)-piperidin-1-yl-methanone

https://huagongshe.com/reaction/1178773

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物HydrazineHCID 9321—
反応物2-[3-(2-Isopropoxy-phenoxy)-propyl]-isoindole-1,3-dioneHCID 67045923—
反応物3-(2-Isopropoxy-phenoxy)-propylamineHCID 67046060—
生成物(3-{[3-(2-Isopropoxy-phenoxy)-propylamino]-methyl}-phenyl)-piperidin-1-yl-methanoneHCID 1125838845%

反応条件

温度50 °C

反応手順

3-(2-Isopropoxy-phenoxy)-propylamine. To a solution of 2-[3-(2-isopropoxy-phenoxy)-propyl]-isoindole-1,3-dione in EtOH (6 mL) was added hydrazine (0.448 g, 14.0 mmol), and the reaction mixture was heated to 50° C. for 30 min. The solvent was removed under reduced pressure, and the crude residue was partitioned between CH2Cl2 (50 mL) and H2O (50 mL). The aqueous layer was extracted with CH2Cl2 (3×50 mL), and the combined organic layers were washed with brine, dried (MgSO4), filtered, and concentrated under reduced pressure. The resulting residue was purified by column chromatography (20-50% EtOAc/hexanes) to provide the desired product (0.267 g, 45%). MS (ESI): mass calculated for C12H19NO2, 209.29. m/z found, 210.2 [M+H]+. 1H NMR (400 MHz, CDCl3): 6.91-6.83 (m, 4H), 4.46 (hept, J=6.1 Hz, 1H), 4.07 (t, J=5.9 Hz, 2H), 2.97 (t, J=6.5 Hz, 2H), 1.99 (quint, J=6.2 Hz, 2H), 1.32 (d, J=6.1 Hz, 6H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07276610B2
出典データセットuspto-grants-2007_10
ORD IDord-fd1904a055c94596a48360254346c4f2
出典メモuspto-grants-2007_10