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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 458566생성일: 2026년 10월 24일

Hydrochloric Acid → 4-Hydroxy-3-methanesulfonyl-1-methyl-1H-quinolin-2-one

https://huagongshe.com/ko/reaction/458566

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium hydrideHCID 24758—
반응물N-Methylisatoic anhydrideHCID 25160—
반응물Ethyl methanesulfonylacetateHCID 78201—
반응물HCID 178418361HCID 178418361—
용매DimethylacetamideHCID 31374—
생성물4-Hydroxy-3-methanesulfonyl-1-methyl-1H-quinolin-2-oneHCID 5468057948%

반응 조건

온도90 °C

반응 단계

A solution of ethylmethanesulfonylacetate (3.78 g, 22.74 mmol) was added slowly in a suspension of sodium hydride (60% in mineral oil, 1.07 g, 25 mmol) in dimethylacetamide under N2 atmosphere. The mixture was allowed to stir at room temperature until the evolution of hydrogen gas ceased, then heated to 90° C. for 30 min and cooled to room temperature. A solution of N-methylisatoic anhydride (4.43 g, 25 mmol) in dimethylacetamide was added slowly and heated overnight at 120° C. The mixture was cooled to room temperature, poured into ice water and acidified by cold 10% HCl. The solids formed were filtered and washed several times by water to yield 2.76 g (48%) of white solids. Mp 170° C. 1H NMR (DMSO-d6): δ 3.51 (s, 3H), 3.59 (s, 3H), 7.39 (t, J=7.4 Hz, 1H), 7.62 (d, J=8.5 Hz, 1H), 7.84 (t, J=7.0 Hz, 1H), 8.09 (d, J=8.0 Hz, 1H). EIMS m/z 254 (M+1), 276 (M+23). Anal. (C11H11NO4S) C, H, N.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07192955B2
출처 데이터셋uspto-grants-2007_03
ORD IDord-a01bf483957a4d1e9b9fd1e7a365f1e1
출처 메모uspto-grants-2007_03