戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 431946作成日:2026年10月25日

2-(Tributylstannyl)pyridine → 3-(2-Pyridyl)-5-(3-cyano-5-(2-pyridyl)phenyl)-1,2,4-oxadiazole

https://huagongshe.com/reaction/431946

反応式

関与物質

役割名称HCID仕込み量
反応物2-(Tributylstannyl)pyridineHCID 607784—
反応物3-(2-Pyridyl)-5-(3-bromo-5-cyanophenyl)-1,2,4-oxadiazoleHCID 9880426—
触媒Tetrakis(triphenylphosphine)palladiumHCID 11979704—
溶媒TetrahydrofuranHCID 8028—
生成物3-(2-Pyridyl)-5-(3-cyano-5-(2-pyridyl)phenyl)-1,2,4-oxadiazoleHCID 992332322%

反応条件

温度100 °C

反応手順

A mixture of 3-(2-pyridyl)-5-(3-bromo-5-cyanophenyl)-1,2,4-oxadiazole (101 mg, 0.31 mmol), tetrakis(triphenylphosphine) palladium(0) (Pd(PPh3)4, 25 mg, 0.021 mmol) and tri-n-butyl(2-pyridyl)tin in tetrahydrofuran (2 mL) was heated overnight at 100° C. The reaction mixture was cooled and transferred directly onto a flash silica column. Elution with a gradient of hexane:ethyl acetate:chloroform 3:1:4 to 2.5:1:4 followed by trituration with hexane in dichloromethane afforded 22 mg (22%) of 3-(2-pyridyl)-5-(3-cyano-5-(2-pyridyl)phenyl)-1,2,4-oxadiazole: 1H NMR (CDCl3): δ-9.12 (s, 1H), 8.88 (d, 1H), 8.78 (d, 1H), 8.64 (s, 1H), 8.61 (s, 1H), 8.26 (d, 1H), 7.89 (m, 3H), 7.51 (m, 1H), 7.40 (m, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06660753B2
出典データセットuspto-grants-2003_12
ORD IDord-703c195b18de4590bb30fd1bc504e876
出典メモuspto-grants-2003_12