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HRID 2254302作成日:2026年10月27日

Sodium Iodide → N-[3-(Quinolin-7-yloxy)propyl]-2,3-dihydro-6,7-methylenedioxy-1,4-benzodioxin-2-methanamine

https://huagongshe.com/reaction/2254302

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium IodideHCID 5238—
反応物DiisopropylethylamineHCID 81531—
反応物7-(3-Bromopropoxy)quinolineHCID 19745014—
反応物2,3-Dihydro-6,7-methylenedioxy-1,4-benzodioxin-2-methanamineHCID 19745017—
溶媒DimethylformamideHCID 6228—
生成物N-[3-(Quinolin-7-yloxy)propyl]-2,3-dihydro-6,7-methylenedioxy-1,4-benzodioxin-2-methanamineHCID 993051857.6%

反応条件

温度80 °C

反応手順

2,3-Dihydro-6,7-methylenedioxy-1,4-benzodioxin-2-methanamine (1.3 g, 6.2 mmole), 7-(3-bromopropoxy)quinoline (1.53 g, 5.5 mmole), diisopropylethylamine 2.6 g, 20 mmole) and sodium iodide (5.5 g, 37 mmole) were combined in 200 ml of DMF and heated at 80° C. for 15 hours under a nitrogen atmosphere. The solvent was then removed in vacuum and replaced with 500 ml of dichloromethane. The mixture was washed with 250 ml each of saturated aqueous sodium bicarbonate and saturated aqueous sodium chloride, dried over sodium sulfate, filtered, and concentrated in vacuum. The residue was column chromatographed on 250 g of silica gel using 3% methanol/dichloromethane as eluant. The product-containing fractions were combined and concentrated in vacuum and the residue (2.25 g) recrystallized from ethanol with the addition of 6 ml of 4N isopropanolic HCl to give 1.25 g of the title compound as a yellow solid dihydrochloride salt, m.p. 224°-226° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05235055
出典データセットuspto-grants-1993_08
ORD IDord-1f3b8dd37368441c944a3642b06276fb
出典メモuspto-grants-1993_08