戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 460215作成日:2026年10月26日

Water → 2-Bromo-6-(4-pyrrolidin-1-ylmethylphenoxy)pyridine

https://huagongshe.com/reaction/460215

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物2,6-DibromopyridineHCID 12274—
反応物Sodium hydrideHCID 24758—
反応物4-(Pyrrolidin-1-ylmethyl)phenolHCID 18771978—
溶媒DimethylformamideHCID 6228—
生成物2-Bromo-6-(4-pyrrolidin-1-ylmethylphenoxy)pyridineHCID 18771652—

反応条件

温度0 °C

反応手順

To a stirred suspension of NaH (2.6 g, 108.5 mmol) in DMF (300 mL) at 0° C., under N2, a solution of 4-pyrrolidin-1-ylmethylphenol (16 g, 90.4 mmol) was added slowly. After stirring at 0° C. for 30 min, 2,6-dibromopyridine (23.6 g, 99.4 mmol) was added and the resulting mixture was heated at 95° C. for 20 h. After cooling to RT, 200 mL of H2O was added and the mixture was extracted with EtOAc (3×300 mL). The combined organic layer was washed with brine (3×400 mL), dried over MgSO4, filtered and concentrated under reduced pressure to yield the title compound as an amber solid. This was used crude in the next step. MS m/z: 333 (M+1). Calc'd for C16H17BrN2O-333.2

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07196104B2
出典データセットuspto-grants-2007_03
ORD IDord-cefd933575fd4c18a2f7015429234586
出典メモuspto-grants-2007_03