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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 918186Generated: October 31, 2026

Chloroacetyl chloride → 3-Chloromethyl-5-bromo-7-sulfamoyl-1,2,4-benzothiadiazine-1,1-dioxide

https://huagongshe.com/reaction/918186

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantHCID 22323981HCID 22323981—
Solvent1,4-DioxaneHCID 31275—
Product3-Chloromethyl-5-bromo-7-sulfamoyl-1,2,4-benzothiadiazine-1,1-dioxideHCID 178514682—

Reaction Steps

A mixture of 2,4-disulfamoyl-6-bromoaniline (0.015 mole) and chloroacetyl chloride (0.016 mole) in 50 ml. of dioxane or other inert organic solvent is heated under reflux conditions for about 24 hours and then concentrated to dryness. The residue is dissolved in concentrated sulfuric acid (5 ml. acid/gram), heated in a steam bath at 60°-70° C. for three hours then poured onto ice. The product, 3-chloromethyl-5-bromo-7-sulfamoyl-1,2,4-benzothiadiazine-1,1-dioxide, is purified by recrystallization from a mixture of acetone-alcohol-water.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03969518
Source datasetuspto-grants-1976_07
ORD IDord-0bb190d64ad84bdc9af6f241939eecf0
Source noteuspto-grants-1976_07