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HRID 2209702作成日:2026年10月26日

Ethanol → N-hydroxy-2-[[4-methoxybenzenesulfonyl](2-quinolinylmethyl)amino]acetamide

https://huagongshe.com/reaction/2209702

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物N-(t-Butyloxy)-2-[[4-methoxybenzenesulfonyl](2-quinolinylmethyl)amino]acetamideHCID 22907171—
溶媒DichloromethaneHCID 6344—
生成物N-hydroxy-2-[[4-methoxybenzenesulfonyl](2-quinolinylmethyl)amino]acetamideHCID 22907131—

反応手順

N-(t-Butyloxy)-2-[[4-methoxybenzenesulfonyl](2-quinolinylmethyl)amino]acetamide (1.15g, 2.42 mmol) is dissolved in methylene chloride (30.0 mL) and ethanol (0.20 mL) in a glass sealed tube. Hydrochloric acid gas (from a lecture bottle) is bubbled through the solution for 20 minutes, and then the tube is sealed and stands at room temperature overnight. The next day, additional hydrochloric acid gas is bubbled through the solution for 20 minutes, more ethanol (0.20 mL) is added, and then the tube is sealed and stands at room temperature for two days. After that time, the solvent is removed. The product is purified by silca gel chromatography (5% to 15% methanol/methylene chloride with ~1% ammonium hydroxide) to give N-hydroxy-2-[[4-methoxybenzenesulfonyl](2-quinolinylmethyl)amino]acetamide, m.p. 177°-178° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05455258
出典データセットuspto-grants-1995_10
ORD IDord-ba3ba135438944c0838d0d7c73b30304
出典メモuspto-grants-1995_10