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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2209702생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/2209702

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물N-(t-Butyloxy)-2-[[4-methoxybenzenesulfonyl](2-quinolinylmethyl)amino]acetamideHCID 22907171—
용매DichloromethaneHCID 6344—
생성물N-hydroxy-2-[[4-methoxybenzenesulfonyl](2-quinolinylmethyl)amino]acetamideHCID 22907131—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05455258
출처 데이터셋uspto-grants-1995_10
ORD IDord-ba3ba135438944c0838d0d7c73b30304
출처 메모uspto-grants-1995_10