戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 597812作成日:2026年10月27日

Water → N-(1-{3-[2-(1-benzothiophen-5-yl)ethoxy]propyl}-3-azetidinyl)acetamide

https://huagongshe.com/reaction/597812

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Ethyl AcetateHCID 8857—
反応物N-(azetidin-3-yl)acetamideHCID 13401968—
反応物5-[2-(3-Chloropropyloxy)ethyl]benzo[b]thiopheneHCID 21990069—
溶媒DimethylformamideHCID 6228—
生成物N-(1-{3-[2-(1-benzothiophen-5-yl)ethoxy]propyl}-3-azetidinyl)acetamideHCID 2354558137.4%

反応条件

温度90 °C

反応手順

0.80 g of 5-(2-(3-chloropropoxy)ethyl)-1-benzothiophene was dissolved in 8 ml of N,N-dimethylformamide. Thereafter, 1.20 g of N-(3-azetidinyl)acetamide was added to the obtained solution, and the obtained mixture was stirred at 90° C. for 12 hours. After cooling, water and ethyl acetate were added to the reaction mixture, and an organic layer was separated. The organic layer was successively washed with water and a saturated saline solution, and then dried over anhydrous magnesium sulfate. Thereafter, the solvent was distilled away under a reduced pressure. The residue was purified by column chromatography (eluent; chloroform:methanol=7:1), so as to obtain 0.39 g of a light yellow oil product, N-(1-(3-(2-(1-benzothiophene-5-yl)ethoxy)propyl)-3-azetidinyl)acetamide.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07897594B2
出典データセットuspto-grants-2011_03
ORD IDord-996ee61b18a94877a3d1ccc2f71f8f95
出典メモuspto-grants-2011_03