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HRID 2043727作成日:2026年10月25日

Citric Acid → 2-{1-[(Tert-butoxy)carbonyl]piperidin-4-yl}-1,3-oxazole-4-carboxylic acid

https://huagongshe.com/reaction/2043727

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WaterHCID 962—
反応物Sodium HydroxideHCID 14798—
反応物Methyl 2-(1-boc-piperidin-4-YL)oxazole-4-carboxylateHCID 67460578—
溶媒Diethyl EtherHCID 3283—
溶媒Sodium ChlorideHCID 5234—
溶媒TetrahydrofuranHCID 8028—
生成物2-{1-[(Tert-butoxy)carbonyl]piperidin-4-yl}-1,3-oxazole-4-carboxylic acidHCID 67461583—

反応条件

温度0 °C

反応手順

1,1-Dimethylethyl 4-[4-(methoxycarbonyl)-2-oxazolyl]-1-piperidinecarboxylate (i.e. the product of Example 7, Step C) (1.41 g, 4.55 mmol) was dissolved in 12 mL tetrahydrofuran, and 8 mL of water was added. The reaction mixture was cooled to 0° C. with vigorous stirring. A 1 N aqueous sodium hydroxide solution (9.1 mL) was added dropwise, and the reaction mixture was stirred at room temperature for 2 h. The mixture was diluted with saturated sodium chloride solution (10 mL), 30 mL of diethyl ether was added and the aqueous phase was acidified to pH 3-4 by dropwise addition of 20% citric acid solution. The precipitated solid was filtered and dried to give 1.21 g of the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08586611B2
出典データセットuspto-grants-2013_11
ORD IDord-f1443203cad24280ad03f35ceefb7173
出典メモuspto-grants-2013_11