戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 382981作成日:2026年10月27日

Potassium Carbonate → 6-(5-Phenyl-1,3,4-oxadiazol-2-yl)methoxy-2-piperidinomethyltetralin hydrochloride

https://huagongshe.com/reaction/382981

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物2-(Chloromethyl)-5-phenyl-1,3,4-oxadiazoleHCID 314941—
反応物6-Hydroxy-2-piperidinomethyltetralinHCID 21939861—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物6-(5-Phenyl-1,3,4-oxadiazol-2-yl)methoxy-2-piperidinomethyltetralin hydrochlorideHCID 2299855369.2%

反応手順

To a solution of 6-hydroxy-2-piperidinomethyltetralin (141 mg, free form of Reference Example 19) and 2-chloromethyl-5-phenyl-1,3,4-oxadiazole (148 mg) in DMF (3 ml) was added potassium carbonate (143 mg) and the reaction mixture was stirred at room temperature for 24 hr. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic layer was washed with water and saturated aqueous sodium chloride, dried, and concentrated. The residue was purified by silica gel column chromatography (eluent: ethyl acetate:methanol=10:1) and alumina column chromatography (eluent: ethyl acetate:hexane=1:4), and then converted into its hydrochloride, which was further recrystallized from methanol-diethyl ether to obtain the titled compound (175 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06310107B1
出典データセットuspto-grants-2001_10
ORD IDord-ce53b8eaa9ab4dfe8a27a4ed5c5660c3
出典メモuspto-grants-2001_10