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HRID 8601作成日:2026年10月23日

Pyridine-4-amidine hydrochloride → 5-(2-Methoxyphenoxy)-2-(4-pyridyl)-tetrahydropyrimidine-4,6-dion

https://huagongshe.com/ja/reaction/8601

反応式

関与物質

役割名称HCID仕込み量
反応物Pyridine-4-amidine hydrochlorideHCID 2776844—
反応物Sodium MethoxideHCID 10942334—
反応物Dimethyl 2-(2-methoxyphenoxy)malonateHCID 12967085—
溶媒MethanolHCID 887—
生成物5-(2-Methoxyphenoxy)-2-(4-pyridyl)-tetrahydropyrimidine-4,6-dionHCID 21979594—
生成物HCID 178419092HCID 178419092—

反応手順

To a stirred solution of sodium methylate (9.7 g) in methanol (100 ml) a solution of dimethyl-(2-methoxyphenoxy)malonate (21.7 g) in methanol (50 ml) was added within 15 min and stirring was continued for 30 min followed by the addition of 4-amidino-pyridine hydrochloride (15 g, Referential Example 2) followed by stirring at room temperature for 20 h. The reaction mixture was concentrated in vacuo. The solid residue was stirred with diethyl ether. The obtained powder was filtered off and dissolved in water (300 ml). Acetic acid was added to pH=4. The precipitated product was filtered off, washed with water and dried in vacuo at 500C. 5-(o-methoxyphenoxy)4,6-dihydroxy-2-(4-pyridyl)pyrimidine (20.1 g, possibly also present as the tautomeric 5-(2-methoxyphenoxy)-2-(4-pyridyl)-tetrahydropyrimidine-4,6-dion) was obtained as a white powder.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091201B2
出典データセットuspto-grants-2006_08
ORD IDord-505c53311be54335b86ddee8a50835c0
出典メモuspto-grants-2006_08