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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1448583Generated: October 31, 2026

2-Aminothiazole → HCID 54717107, compound

https://huagongshe.com/reaction/1448583

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
ReactantHCID 54717108HCID 54717108—
SolventO-XyleneHCID 7237—
ProductHCID 54717107HCID 54717107—

Reaction Steps

0.4 g. of 6-chloro-4-hydroxy-2-methyl-3-methoxycarbonyl-2H-thieno[3,2-e]1,2-thiazine-1,1-dioxide is heated under reflux for 16 hours with 0.19 g. of 2-aminothiazole in 45 ml. of absolute xylene, while passing a stream of nitrogen through the mixture. The reaction mixture is cooled to room temperature, and the product is crystallized out by scratching and then kept overnight in the cold. The precipitate crystals are removed by filtration under suction, recrystallized from ethanol, and 6-chloro-4-hydroxy-2-methyl-3-(2-thiazolecarbamoyl)-2H-thieno[3,2-e]1,2-thiazine-1,1-dioxide having a melting point of 136°-138° (with decomposition) is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04180662
Source datasetuspto-grants-1979_12
ORD IDord-67867f60e15e402fb94fb30741a4c97f
Source noteuspto-grants-1979_12