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HRID 1166534作成日:2026年10月26日

Sodium Chloride → 6-(3'-Aminobiphenyl-4-yl)methoxy-2-[2-(N,N-dimethylamino)ethyl]tetralin hydrochloride

https://huagongshe.com/reaction/1166534

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium ChlorideHCID 5234—
反応物Sodium CarbonateHCID 10340—
反応物6-(4-bromobenzyl)oxy-2-[2-(N,N-dimethylamino)ethyl]tetralinHCID 18361484—
反応物3-Aminophenylboric acidHCID 21895836—
触媒Tetrakis(triphenylphosphine)palladiumHCID 11979704—
溶媒EthanolHCID 702—
溶媒TolueneHCID 1140—
生成物6-(3'-Aminobiphenyl-4-yl)methoxy-2-[2-(N,N-dimethylamino)ethyl]tetralin hydrochlorideHCID 18361523—

反応手順

An ethanol solution (10 ml) of 3-aminophenylboric acid (1.3 g) and an aqueous 2M sodium carbonate solution (10 ml) were added to a toluene solution (80 ml) of 6-(4-bromobenzyl)oxy-2-[2-(N,N-dimethylamino) ethyl]tetralin (3.00 g) and tetrakis-(triphenylphosphine) palladium (0.45 g). The reaction mixture was heated under reflux for 12 hours in an argon atmosphere. A saturated aqueous sodium chloride solution was added to this, which was then extracted with ethyl acetate. The organic layer was dried, and then concentrated. The residue was purified by alumina column chromatography (eluent: ethyl acetate/hexane=1/2), and then processed with 4 N hydrochloric acid-ethyl acetate to form a hydrochloride. The thus-formed salt was recrystallized from methanol-diisopropyl ether to obtain the entitled compound (0.78 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06613805B2
出典データセットuspto-grants-2003_09
ORD IDord-03c15fedcc0548d2ab238ed924c81311
出典メモuspto-grants-2003_09