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HRID 384111作成日:2026年10月25日

Citric Acid → HCID 178515652、化合物

https://huagongshe.com/reaction/384111

反応式

関与物質

役割名称HCID仕込み量
反応物Citric AcidHCID 311—
反応物Hydroxyamine hydrochlorideHCID 443297—
反応物Sodium hydroxide methanolHCID 23721981—
反応物Ethyl 2,3-dibromo-3-(5-((2-phenoxybenzyl)oxy)-2-pyridinyl)propanoateHCID 86641941—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 178515652HCID 178515652—

反応手順

To a solution of ethyl 2,3-dibromo-3-(5-((2-phenoxybenzyl)oxy)-2-pyridinyl)propanoate (159.3 mg) in tetrahydrofuran (1 ml), 32 mg of hydroxyamine hydrochloride, 0.6 ml of 2.5N sodium hydroxide/methanol solution and 0.078 ml of water were added, and the reaction solution was stirred at room temperature for 2 hours and then heated to reflux overnight. The reaction solution was cooled, then diluted with water, acidified with 10% aqueous citric acid, then extracted with chloroform, and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the residue obtained was purified through reversed phase medium pressure liquid chromatography (ODS-AS-360-CC (by YMC), mobile phase: water-acetonitrile-0.1% trifluoroacetic acid). The solvent of the resultant fraction was distilled off under reduced pressure, and then purification by preparative thin layer chromatography (Kieselgel™ 60 F254, Art5744, made by Merck & Co., chloroform/methanol (9:1)) was carried out to afford the title compound as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08367708B2
出典データセットuspto-grants-2013_02
ORD IDord-112f29fe81dd45acbbafa00569fa008b
出典メモuspto-grants-2013_02