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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264318Generated: November 3, 2026

Methanol → HCID 57837885, compound

https://huagongshe.com/reaction/2264318

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantDimethylformamideHCID 6228—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantHCID 68706219HCID 68706219—
SolventWaterHCID 962—
ProductHCID 57837885HCID 57837885—

Reaction Steps

In 11.5 ml of DMF was dissolved 500 mg of 6-nitro-2H-benzothiazin-3(4H)-one, and thereto was added 114 mg of sodium hydride of 55% purity under ice cooling, followed by 30 minutes of stirring at room temperature. To the reaction solution was added 444 μl of methyl iodide, and the whole was stirred at room temperature for 2 hours. To the reaction solution was added 2 ml of methanol under ice cooling, followed by 10 minutes of stirring at room temperature. Thereafter, water was added and the organic layer was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and then the solvent was removed by evaporation. The obtained residue was purified by silica gel column chromatography (chloroform) to obtain 308 mg of 4-methyl-6-nitro-2H-1,4-benzothiazin-3(4H)-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855198B2
Source datasetuspto-grants-2010_12
ORD IDord-e70ca454f87e4a54ad06fcc80cc9fa42
Source noteuspto-grants-2010_12