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HRID 1662020作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/1662020

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US08030302B2
出典データセットuspto-grants-2011_10
ORD IDord-57e49fb0763f41c6a6b13c00bfa96d11
出典メモuspto-grants-2011_10