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HRID 1066495作成日:2026年10月27日

Ethanol → 5-Methyl-pyridine-2-sulfonic acid [2-(3-hydroxy-phenyl)-6-methoxy-5-(2-methoxy-phenoxy)-pyrimidin-4-yl]-amide

https://huagongshe.com/reaction/1066495

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物1,3-CyclohexadieneHCID 11605—
反応物5-Methyl-pyridine-2-sulfonic acid [2-(3-benzyloxy-phenyl)-6-methoxy-5-(2-methoxy-phenoxy)-pyrimidin-4-yl]-amideHCID 53801719—
触媒PalladiumHCID 23938—
溶媒1,4-DioxaneHCID 31275—
生成物5-Methyl-pyridine-2-sulfonic acid [2-(3-hydroxy-phenyl)-6-methoxy-5-(2-methoxy-phenoxy)-pyrimidin-4-yl]-amideHCID 9848584—

反応手順

1.46 g of 5-methyl-pyridine-2-sulfonic acid [2-(3-benzyloxy-phenyl)-6-methoxy-5-(2-methoxy-phenoxy)-pyrimidin-4-yl]-amide were dissolved in dioxane (25 ml) by gentle warming than ethanol (50 ml) was added followed by cyclohexadiene (6 g) and palladium on charcoal, 10%, (1.46 g). The solution was refluxed for 20 h, the catalyst removed by filtration and the solution concentrated on a rotary evaporator. The yellow crystalline solid that precipitated was collected, washed with ether and dried in a vacuum to give the desired 5-methyl-pyridine-2-sulfonic acid [2-(3-hydroxy-phenyl)-6-methoxy-5-(2-methoxy-phenoxy)-pyrimidin-4-yl]-amide as off-white crystals. ISP mass spectrum, m/e 495.2 (M+1 calculated for C24H22N4O6S1: 495). Melting point 211°-216° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06242601B1
出典データセットuspto-grants-2001_06
ORD IDord-d4d00f622d1a4fadaad775f5f73fa339
出典メモuspto-grants-2001_06