戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1014277作成日:2026年10月26日

Tetrahydrofuran → 1-[2-(dimethylamino)ethyl]-5-(methyloxy)-2,3-dihydro-1H-indol-6-amine

https://huagongshe.com/reaction/1014277

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物Aluminium lithium hydrideHCID 21226445—
反応物1-(6-Amino-5-methoxy-2,3-dihydro-1H-indol-1-yl)-2-(dimethylamino)ethan-1-oneHCID 53414764—
溶媒Diethyl EtherHCID 3283—
溶媒Ethyl AcetateHCID 8857—
生成物1-[2-(dimethylamino)ethyl]-5-(methyloxy)-2,3-dihydro-1H-indol-6-amineHCID 5944212925%

反応条件

温度50 °C

反応手順

A 1.0M solution of lithium aluminum hydride in diethyl ether (Aldrich, 11 mL, 11 mmol, 10 equiv.) was added dropwise to a solution of 1-[(dimethylamino)acetyl]-5-(methyloxy)-2,3-dihydro-1H-indol-6-amine (0.280 g, 1.12 mmol) in diethyl ether (10 mL). The solids failed to dissolve, so anhydrous tetrahydrofuran was added (10 mL) and the solution was maintained at 50° C. for 12 hours. The solution was cooled, poured into ice water, diluted with ethyl acetate, and the organic layer was dried, taken to a residue under reduced pressure, and purified by chromatography on SiO2 to afford 1-[2-(dimethylamino)ethyl]-5-(methyloxy)-2,3-dihydro-1H-indol-6-amine (0.065 g, 25% Yield). 1H NMR (400 MHz, CDCl3) δ ppm 6.66 (s, 1 H), 6.05 (s, 1 H), 3.77 (s, 3 H), 3.28 (t, J=8.07 Hz, 2 H), 3.16 (t, J=6.97 Hz, 2 H), 2.86 (t, J=8.25 Hz, 2H), 2.64 (s, 2 H), 2.39 (s, 6 H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07981903B2
出典データセットuspto-grants-2011_07
ORD IDord-06825cde5e48477bb6ac4c73b7d0421c
出典メモuspto-grants-2011_07