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HRID 564102作成日:2026年10月26日

Pyridine → 1-[2-(4-chloromethylphenyl)-2-oxo-ethyl]-4-(4-fluoro-benzyloxy)-1H-pyridin-2-one

https://huagongshe.com/reaction/564102

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物Thionyl ChlorideHCID 24386—
反応物4-(4-Fluoro-benzyloxy)-1-[2-(4-hydroxymethyl-phenyl)-2-oxo-ethyl]-1H-pyridin-2-oneHCID 58042834—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物1-[2-(4-chloromethylphenyl)-2-oxo-ethyl]-4-(4-fluoro-benzyloxy)-1H-pyridin-2-oneHCID 58042703—

反応条件

温度0 °C

反応手順

To 1.20 g (3.27 mmol) 4-(4-fluoro-benzyloxy)-1-[2-(4-hydroxymethyl-phenyl)-2-oxo-ethyl]-1H-pyridin-2-one (preparation 31.1) in 20 mL DCM is added 0.29 mL (3.59 mmol) pyridine and 0.26 mL (3.59 mmol) thionylchloride at 0° C. The reaction mixture is stirred 1 h at 0° C., is warmed to RT and is then diluted with water. The organic phase is washed with saturated aqueous KHSO4-solution and then with water, dried over MgSO4, filtered over charcoal and the solvent is evaporated.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08067590B2
出典データセットuspto-grants-2011_11
ORD IDord-e661e0376b52405a962b4a9660afb778
出典メモuspto-grants-2011_11