戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1992402作成日:2026年10月26日

Acetonitrile → 4-Cyano-N-(2-{7-[2-(2-fluoro-phenoxy)-ethyl]-9-oxa-3,7-diazabicyclo[3.3.1]non-3-yl}-ethyl)-N-methyl-benzenesulfonamide

https://huagongshe.com/reaction/1992402

反応式

関与物質

役割名称HCID仕込み量
反応物AcetonitrileHCID 6342—
反応物Potassium CarbonateHCID 11430—
反応物1-(2-Bromoethoxy)-2-fluorobenzeneHCID 2386106—
反応物4-cyano-N-methyl-N-[2-(9-oxa-3,7-diaza-bicyclo[3.3.1]non-3-yl)-ethyl]-benzenesulfonamide dihydrochlorideHCID 68520931—
溶媒WaterHCID 962—
生成物4-Cyano-N-(2-{7-[2-(2-fluoro-phenoxy)-ethyl]-9-oxa-3,7-diazabicyclo[3.3.1]non-3-yl}-ethyl)-N-methyl-benzenesulfonamideHCID 6852080058%

反応条件

温度160 °C

反応手順

To 4-cyano-N-methyl-N-[2-(9-oxa-3,7-diaza-bicyclo[3.3.1]non-3-yl)-ethyl]-benzenesulfonamide dihydrochloride (0.127 g, 0.30 mmol, prep I above), 1-(2-bromo-ethoxy)-2-fluoro-benzene (0.069 g, 0.315 mmol;) and potassium carbonate (0.145 g, 1.05 mmol) was added acetonitrile (4 mL) and water (0.1 mL). The mixture was heated by microwave irradiation (10 minutes, 160° C.) and was then filtered and evaporated. The crude product was purified by chromatography on silica gel using methanol saturated with ammonia in dichloromethane as eluent, which afforded 85 mg (58.0%) of the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07648985B2
出典データセットuspto-grants-2010_01
ORD IDord-fec54478f9c04f31973031cb30395e37
出典メモuspto-grants-2010_01