戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1594846作成日:2026年10月27日

Cesium carbonate → 4-Imidazol-1-ylmethyl-2-[2-(2-oxo-piperidin-1-yl)-phenoxy]-benzonitrile

https://huagongshe.com/reaction/1594846

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物1-(2-Hydroxyphenyl)piperidin-2-oneHCID 11506609—
反応物Benzonitrile, 2-fluoro-4-(1H-imidazol-1-ylmethyl)-HCID 21697068—
溶媒DimethylformamideHCID 6228—
生成物4-Imidazol-1-ylmethyl-2-[2-(2-oxo-piperidin-1-yl)-phenoxy]-benzonitrileHCID 9799607—

反応条件

温度50 °C

反応手順

2-Fluoro-4-imidazol-1-ylmethyl-benzonitrile (as described in Step E above) (0.080 g, 0.4 mmol), 2-(2-oxo-piperidin-1-yl)-phenol (as described in Step F above) (0.091 g, 0.5 mmol) and cesium carbonate (0.261 g, 0.8 mmol) were combined in DMF (2.0 mL) and heated at 50° C. for 18 hr. The reaction mixture was partitioned between EtOAc and a minimum volume of H2O. Additional product was salted out from the aqueous layer with solid NaCl, and extracted into EtOAc. The organic layers were combined, dried (Na2SO4), filtered and concentrated to give the title compound after RP HPLC on a Waters Prep Pak column eluting with a 0.1% TFA/H2O: 0.1% TFA/CH3CN gradient followed by conversion to the free base.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06284755B1
出典データセットuspto-grants-2001_09
ORD IDord-764d005d84154974a976aba09e644e7d
出典メモuspto-grants-2001_09