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HRID 2195536作成日:2026年10月26日

Pyridine → Ethyl 4,6-dimethyl-2-oxo-1-phenyl-1,2-dihydropyridine-3-carboxylate

https://huagongshe.com/reaction/2195536

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物Phenylboronic AcidHCID 66827—
反応物Ethyl 4,6-dimethyl-2-oxo-1,2-dihydropyridine-3-carboxylateHCID 247443—
溶媒1,4-DioxaneHCID 31275—
生成物Ethyl 4,6-dimethyl-2-oxo-1-phenyl-1,2-dihydropyridine-3-carboxylateHCID 1383792531.2%

反応条件

温度80 °C

反応手順

A suspension of ethyl 4,6-dimethyl-2-oxo-1,2-dihydropyridine-3-carboxylate (7.5 g, 0.038 mol), phenylboronic acid (14.1 g, 0.115 mol), cupric acetate (1.38 g, 0.008 mol), pyridine (7.5 mL) in 1,4-dioxane (80 mL) is heated at 80° C. for 96 hours. The solid is filtered off and the filtrate is concentrated. The residue is partitioned with EtOAc (50 mL) and 2N HCl (70 mL), and the precipitate is collected by filtration and washed with EtOAc to give the title product (2.95 g). The EtOAc solution is separated, dried and concentrated. The residue is purified by silica gel column chromatography eluting with PE:acetone (2:1) to give another portion of (0.3 g). (3.25 g, 31.2% yield). MS (m/z): 272.0 (M+H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号USRE043878E1
出典データセットuspto-grants-2012_12
ORD IDord-499c94a7e3e545b7aedb83d98329b027
出典メモuspto-grants-2012_12