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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 224603Generated: November 1, 2026

2-Amino-5-methylthiazole → HCID 54683005, compound

https://huagongshe.com/reaction/224603

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-5-methylthiazoleHCID 351770—
ReactantHCID 54703139HCID 54703139—
SolventO-XyleneHCID 7237—
ProductHCID 54683005HCID 5468300577%

Reaction Steps

5.0 gm (16.5 millimols) of methyl 6-chloro-4-hydroxy-2-methyl-2H-1,2-benzothiazine-3-carboxylate-1,1-dioxide and 2.1 gm (18.5 millimols) of 2-amino-5-methyl-thiazole were refluxed in 300 ml of anhydrous xylene for 24 hours in a Soxhlet-apparatus equipped with a 4-A-molecular sieve. After cooling, the crude product which had crystallized out was filtered off and recrystallized from dioxane. 4.9 gm (77% of theory) of 6-chloro-4-hydroxy-2-methyl-N-(5-methyl-2-thiazolyl)-2H-1,2-benzothiazine-3-carboxamide-1,1-dioxide were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04233299
Source datasetuspto-grants-1980_11
ORD IDord-98bd6dd378b24008b104a99a88bf6b80
Source noteuspto-grants-1980_11