戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 411526作成日:2026年10月26日

Potassium Carbonate → 4-({3-[3-Azabicyclo[3.2.1]oct-8-yl(methyl)amino]propyl}amino)benzonitrile

https://huagongshe.com/reaction/411526

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3-benzyl-N-methyl-3-azabicyclo[3.2.1]octan-8-amineHCID 18541030—
反応物3-(4-Cyanoanilino)propyl 4-methylbenzenesulfonateHCID 21867652—
溶媒DimethylformamideHCID 6228—
生成物4-({3-[3-Azabicyclo[3.2.1]oct-8-yl(methyl)amino]propyl}amino)benzonitrileHCID 1854090765.5%

反応条件

温度90 °C

反応手順

A mixture of 3-benzyl-N-methyl-3-azabicyclo[3.2.1]octan-8-amine (Preparation B; 4.0 g, 17.4 mmol), 3-(4-cyanoanilino)propyl 4-methyl-benzenesulfonate (Preparation G(ii); 5.74 g, 17.4 mmol), and potassium carbonate (2.40 g, 17.4 mmol) in DMF (85 mL) was heated at 90° C. under nitrogen overnight. The mixture was partitioned with water (200 mL) and diethyl ether (150 mL). The aqueous layer was extracted with ethyl acetate (2×50 mL). The combined organic extracts were washed with brine (2×30 mL), dried (Na2SO4), filtered and then concentrated in vacuo. The residue was chromatographed on silica gel, eluting with dichloromethane:methanol (98:2), to afford 3.40 g (50%) of the sub-title compound as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06559162B2
出典データセットuspto-grants-2003_05
ORD IDord-159d2fdcc8c34753ace01f967dbd9955
出典メモuspto-grants-2003_05