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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2163441Generated: October 30, 2026

2-Aminothiazole → HCID 54704472, compound

https://huagongshe.com/reaction/2163441

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
ReactantHCID 54704473HCID 54704473—
SolventO-XyleneHCID 7237—
ProductHCID 54704472HCID 5470447221.3%

Reaction Conditions

Temperature5 °C

Reaction Steps

A mixture of methyl 4-hydroxy-6H-thieno[2,3-b]thiopyran-5-carboxylate 7,7-dioxide (5.2 g, 0.02 mole), 2-aminothiazole (3.0 g, 0.03 mole) and xylene (175 ml) is warmed and filtered from the polymeric products. The filtrate is refluxed for 30 min. when some more polymeric product is formed. It is filtered again, and the filtrate refluxed for 1.5 hrs. The mixture is cooled to 5° C. in an ice-bath, and the resulting crystalline product is collected. It is dissolved in THF, treated with charcoal and filtered. The filtrate is concentrated to give the desired product (1.4 g, 21%), m.p. 215-216° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04134897
Source datasetuspto-grants-1979_01
ORD IDord-25955de9ebd14bbf8dbde177627a4a38
Source noteuspto-grants-1979_01