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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 224599Generated: October 29, 2026

2-Amino-5-methylthiazole → 2,6-Dimethyl-4-hydroxy-N-(5-methyl-2-thiazolyl)-2H-1,2-benzothiazine-3-carboxamide-1,1-dioxide

https://huagongshe.com/reaction/224599

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-5-methylthiazoleHCID 351770—
Reactantmethyl 4-hydroxy-2,6-dimethyl-2H-1,2-benzothiazine-3-carboxylate-1,1-dioxideHCID 54696079—
SolventO-XyleneHCID 7237—
Product2,6-Dimethyl-4-hydroxy-N-(5-methyl-2-thiazolyl)-2H-1,2-benzothiazine-3-carboxamide-1,1-dioxideHCID 54694221—

Reaction Steps

4.0 gm (14 millimols) of methyl 4-hydroxy-2,6-dimethyl-2H-1,2-benzothiazine-3-carboxylate-1,1-dioxide and 2.0 gm (17 millimols) of 2-amino-5-methyl-thiazole were refluxed in 200 ml of anhydrous xylene for 24 hours. After cooling, the crystals which had separated out were filtered off. After recrystallization from ethylene chloride 3.6 gm (70% of theory) of 2,6-dimethyl-4-hydroxy-N-(5-methyl-2-thiazolyl)-2H-1,2-benzothiazine-3carboxamide-1,1-dioxide were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04233299
Source datasetuspto-grants-1980_11
ORD IDord-193861cfc36a487aa1ee9cd683e467d0
Source noteuspto-grants-1980_11