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HRID 7442作成日:2026年10月23日

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

https://huagongshe.com/ja/reaction/7442

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

In 8 mL of N,N-dimethylformamide was dissolved 0.80 g of 5-[2-(3-chloropropoxy)ethyl]-1-benzothiophene, and 1.20 g of N-(3-azetidinyl)acetamide was added to the solution, after which the resulting mixture was stirred at 90° C. for 12 hours. After the reaction mixture was cooled, water and ethyl acetate were added thereto and the organic layer was separated. The organic layer was washed with water and then a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and then distilled under reduced pressure to remove the solvent. The residue was purified by a column chromatography (eluent; chloroform:methanol=7:1) to obtain 0.39 g of N-(1-{3-[2-(1-benzothiophen-5-yl)ethoxy]propyl}-3-azetidinyl)acetamide as a light-yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087594B2
出典データセットuspto-grants-2006_08
ORD IDord-8598c28fdc514017867c427eb14f28f6
出典メモuspto-grants-2006_08