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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1720612생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1720612

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 (1.15 g, 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 silica 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 번호US05506242
출처 데이터셋uspto-grants-1996_04
ORD IDord-c405b43fa55c429b9198e555f3e339ba
출처 메모uspto-grants-1996_04