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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6691Generated: October 25, 2026

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

https://huagongshe.com/reaction/6691

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
ReactantN-Methylisatoic anhydrideHCID 25160—
ReactantEthyl methanesulfonylacetateHCID 78201—
ReactantHCID 178418361HCID 178418361—
SolventDimethylacetamideHCID 31374—
Product4-Hydroxy-3-methanesulfonyl-1-methyl-1H-quinolin-2-oneHCID 5468057948%

Reaction Conditions

Temperature90 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07084141B2
Source datasetuspto-grants-2006_08
ORD IDord-157b7894b4f7449aa2714755436d2131
Source noteuspto-grants-2006_08