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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 224608Generated: October 29, 2026

Iodoethane → 2-Ethyl-4-hydroxy-N-(5-methyl-2-thiazolyl)-2H-1,2-benzothiazine-3-carboxamide-1,1-dioxide

https://huagongshe.com/reaction/224608

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
Reactant4-Hydroxy-N-(5-methyl-2-thiazolyl)-2H-1,2-benzothiazine-3-carboxamide-1,1-dioxideHCID 54690657—
SolventMethanolHCID 887—
SolventSodium HydroxideHCID 14798—
Product2-Ethyl-4-hydroxy-N-(5-methyl-2-thiazolyl)-2H-1,2-benzothiazine-3-carboxamide-1,1-dioxideHCID 5469013848%

Reaction Steps

0.94 gm (6 millimols) of ethyl iodide were added to a solution of 0.7 gm (2 millimols) of 4-hydroxy-N-(5-methyl-2-thiazolyl)-2H-1,2-benzothiazine-3-carboxamide-1,1-dioxide in 30 ml of methanol and 2.0 ml of 1N sodium hydroxide. The reaction mixture was stirred for 24 hours at room temperature, then neutralized and evaporated in vacuo. The residue was purified by column chromatography (Merck-silica gel 60, particle size: 0.2-0.5 mm; eluant: chloroform/ethanol 95:5), yielding 0.35 mgm (48% of theory) of 2-ethyl-4-hydroxy-N-(5-methyl-2-thiazolyl)-2H-1,2-benzothiazine-3-carboxamide-1,1-dioxide after recrystallization from xylene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04233299
Source datasetuspto-grants-1980_11
ORD IDord-7e8dbc42e9ab41089cf19bcbf3bdcc76
Source noteuspto-grants-1980_11