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HRID 382980作成日:2026年10月26日

Potassium Carbonate → 2-(N,N-Dimethylamino)methyl-6-(5-phenyl-1,3,4-oxadiazol-2-yl)methoxytetralin

https://huagongshe.com/reaction/382980

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2-(N,N-Dimethylamino)methyl-6-hydroxytetralinHCID 21939764—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物2-(N,N-Dimethylamino)methyl-6-(5-phenyl-1,3,4-oxadiazol-2-yl)methoxytetralinHCID 18361571—

反応手順

To a solution of 2-(N,N-dimethylamino)methyl-6-hydroxytetralin (206 mg, a free form of Reference Example 16) and 2-chloromethyl-5-phenyl-1,3,4-oxadiazole (231 mg) in DMF (5 ml) was added potassium carbonate (215 mg) and the reaction mixture was stirred at room temperature for 15 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 alumina column chromatography (eluent: ethyl acetate:hexane=1:2) to obtain the titled compound (307 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-401c1e281b75427c8800002863c66290
出典メモuspto-grants-2001_10