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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066154Generated: October 31, 2026

Methyl iodide → 7-Chloro-4-methyl-3-methylsulfanyl-4H-1,2,4-benzothiadiazine 1,1-dioxide

https://huagongshe.com/reaction/1066154

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant7-Chloro-3-(methylthio)-4H-benzo[e][1,2,4]thiadiazine 1,1-dioxideHCID 12700106—
SolventMethanolHCID 887—
SolventAcetonitrileHCID 6342—
Product7-Chloro-4-methyl-3-methylsulfanyl-4H-1,2,4-benzothiadiazine 1,1-dioxideHCID 21197804—

Reaction Steps

A solution of 7-chloro-3-methylsulfanyl-4H-1,2,4-benzothiadiazine 1,1-dioxide (0.8 g) in acetonitrile (24 mL) and methanol (0.5 mL) was supplemented with potassium carbonate (0.96 g), then with methyl iodide (3 mL), and stirred at room temperature for 10 h. The solvent was removed by distillation under reduced pressure. The residue was suspended in water (40 mL) and the pH was adjusted to pH 2 with formic acid. The precipitate of the title compound was collected by filtration, washed with water and dried. The compound was used without further purification in the next step (yield: 0.53 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06242443B1
Source datasetuspto-grants-2001_06
ORD IDord-11bd17b8349c44cca3c109fcea3c9034
Source noteuspto-grants-2001_06