戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 713713作成日:2026年10月24日

Sodium hydride → Tert-butyl 4-(pyridin-2-ylmethyl)piperazine-1-carboxylate

https://huagongshe.com/ja/reaction/713713

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物tert-Butyl piperazine-1-carboxylateHCID 143452—
反応物2-(Bromomethyl)pyridineHCID 564209—
溶媒DimethylformamideHCID 6228—
生成物Tert-butyl 4-(pyridin-2-ylmethyl)piperazine-1-carboxylateHCID 10062065—

反応手順

To a stirred suspension of 0.28 g (0.71 mmol) of sodium hydride (60% mineral oil dispersion) in 5 mL anhydrous N,N-dimethylformamide at 0° C. was added 0.12 g (0.65 mmol) tert-butyl 1-piperazine-carboxylate. The resulting mixture was stirred under an atmosphere of nitrogen for 15 min and then allowed to warm to ambient temperature at which point 0.14 g (0.59 mmol) of 2-(bromomethyl)pyridine was added. After 4 h, quench the reaction with 25 mL cold water and extract the resulting solution with 25 mL ethyl acetate. The organic layer was washed with water (2×25 mL), dried over magnesium sulfate, filtered and evaporated in vacuo to afford the title compound which was purified by reverse-phase HPLC (TMC Pro-Pac C18; 10-100% 0.1% trifluoroacetic acid in acetonitrile/0.1% trifluoroacetic acid in water gradient). LC/MS: m/z (ES) 278.1 (MH)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09186354B2
出典データセットuspto-grants-2015_11
ORD IDord-1730713aafb74215b6b84f71721337e5
出典メモuspto-grants-2015_11