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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 459794Generated: October 30, 2026

Sulfamide → 5-bromo-3-methyl-3,4-dihydro-1H-benzo[1,2,6]thiadiazine 2,2-dioxide

https://huagongshe.com/reaction/459794

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfamideHCID 82267—
Reactant3-Bromo-2-methylaminomethyl-phenylamineHCID 18444472—
SolventPyridineHCID 1049—
Product5-bromo-3-methyl-3,4-dihydro-1H-benzo[1,2,6]thiadiazine 2,2-dioxideHCID 58824127—

Reaction Steps

To a solution of 3-bromo-2-methylaminomethyl-phenylamine from step 3 of Example 3 (2.615 g, 12.2 mmol) in pyridine (50 ml) was added sulfamide (3.5 g, 36.4 mmol). The solution was heated under reflux overnight, and the cooled reaction mixture was partitioned between 2N HCl water solution and ethyl acetate. The organic layer was washed with 2N HCl solution, water, brine. After drying over MgSO4, the organic fraction was concentrated in vacuo and resulting brown residue was purified by flash chromatography to give 5-bromo-3-methyl-3,4-dihydro-1H-benzo[1,2,6]thiadiazine 2,2-dioxide as a white solid. (2.32 g, 69%) MS: (M+H)+277.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07196087B2
Source datasetuspto-grants-2007_03
ORD IDord-b85f84d2dd6d420db009c3e6e24567fc
Source noteuspto-grants-2007_03