戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 101作成日:2026年10月23日

Piperazine, 2-pyridylethyl- → Ethyl 7-(4-(2-(pyridin-2-yl)ethyl)piperazin-1-yl)benzofuran-2-carboxylate

https://huagongshe.com/ja/reaction/101

反応式

関与物質

役割名称HCID仕込み量
反応物Piperazine, 2-pyridylethyl-HCID 566605—
反応物Ethyl 7-bromobenzofuran-2-carboxylateHCID 46738833—
試薬Cesium carbonateHCID 10796—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
触媒2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
溶媒1,4-DioxaneHCID 31275—
生成物Ethyl 7-(4-(2-(pyridin-2-yl)ethyl)piperazin-1-yl)benzofuran-2-carboxylateHCID 5963675139.97%

反応条件

温度95 °C

反応手順

12/01 2009 15:21:58 +0100 To ethyl 7-bromobenzofuran-2-carboxylate (0.900 g, 3.34 mmol) and 1-(2-(pyridin-2-yl)ethyl)piperazine (0.672 g, 3.51 mmol) in dry degassed dioxane (13 mL) were added Cesium carbonate (1.417 g, 4.35 mmol), 2-Dicyclohexylphosphino-2',4',6'-triisopropylbiphenyl (0.159 g, 0.33 mmol) and Tris(dibenzylideneacetone)dipalladium(0) (0.153 g, 0.17 mmol) under argon and the reaction heated at 95°C o/n. All starting material consumed. Water and DCM were added and the layers separated. The aq phase was extracted with DCM (3x). The combined org phases were washed with water, dried (MgSO4), filtered and evaporated. The crude was purified by flash chrom. (SiO2; DCM/MeOH 95/5) to give EN02198-25-001: 47.3 mg (fraction 12 from the flash) of the product as a pale yellow solid. This batch was submitted to test. EN02198-25-002: 0.460 g (fractions 11 and 13-18 from the flash) of the product as a pale brown solid.

情報源と証拠

出典データセット750 AstraZeneca ELN dataset
ORD IDord-61dd76cabf5f48cb8028fe718c7f9d72
出典メモ750 AstraZeneca ELN dataset