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HRID 33771作成日:2026年10月24日

Carbon Dioxide → (+/-)-N-[4-(Dimethylamino)benzyl]-N-(4-isopropylphenyl)-2-methoxy-5,6,7,8-tetrahydroquinoline-8-carboxamide

https://huagongshe.com/ja/reaction/33771

反応式

関与物質

役割名称HCID仕込み量
反応物Carbon DioxideHCID 280—
反応物DimethylformamideHCID 6228—
反応物4-MethylmorpholineHCID 7972—
反応物Propylphosphonic acidHCID 204484—
反応物2-Methoxy-5,6,7,8-tetrahydroquinolineHCID 18180283—
反応物N-(4-(Dimethylamino)benzyl)-4-isopropylbenzenamineHCID 21957887—
反応物Sodium bicarbonate ethyl acetateHCID 86584982—
反応物HCID 178418306HCID 178418306—
溶媒Diethyl EtherHCID 3283—
生成物(+/-)-N-[4-(Dimethylamino)benzyl]-N-(4-isopropylphenyl)-2-methoxy-5,6,7,8-tetrahydroquinoline-8-carboxamideHCID 11576159—

反応条件

温度0 °C

反応手順

To a 0.22 M solution of 2-methoxy-5,6,7,8-tetrahydroquinoline in Et2O at −78° C. was added 1.7 equiv of t-BuLi [1,7M] over 5 min. After allowing the reaction to warm up to 0° C. and stirring at this temperature for 30 min, a stream of CO2(g) was then allowed to flow into the flask. The final mixture was allowed to warm to room temperature and the solvent was removed by the flow of CO2. To a solution/suspension of the resulting crude lithium carboxylate salt in DMF (12 equiv) at 0° C. was successively added 1.2 equiv of N-[4-(dimethylamino)benzyl]4-isopropylaniline, 12 equiv of 4-methylmorpholine and 4.0 equiv of 1-propylphosphonic acid cyclic anhydride (50% in EtOAc). After allowing the reaction to warm to room temperature overnight, this mixture was poured into a separatory funnel containing aqueous NaHCO3/EtOAc. The organic layer was washed with brine, dried over anhydrous MgSO4, filtered and concentrated. The crude material was further purified by flash chromatography, eluting with a gradient from 100% hexanes to 25% EtOAc/hexanes to provide the title compound as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07429666B2
出典データセットuspto-grants-2008_09
ORD IDord-ea7852a2269f4205a78fa8db6484b238
出典メモuspto-grants-2008_09