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HRID 14358作成日:2026年10月25日

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

https://huagongshe.com/reaction/14358

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Sodium hydrideHCID 24758—
反応物N-Methylisatoic anhydrideHCID 25160—
反応物Ethyl methanesulfonylacetateHCID 78201—
反応物HCID 178418361HCID 178418361—
溶媒DimethylacetamideHCID 31374—
生成物4-Hydroxy-3-methanesulfonyl-1-methyl-1H-quinolin-2-oneHCID 5468057948%

反応条件

温度90 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732146B2
出典データセットuspto-grants-2010_06
ORD IDord-086946a7c8894b269f4f76e3f6f2650b
出典メモuspto-grants-2010_06