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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1704638Generated: November 3, 2026

2-Aminothiazole → HCID 54704472, compound

https://huagongshe.com/reaction/1704638

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 numberUS04127585
Source datasetuspto-grants-1978_11
ORD IDord-5191af4e53c744dda14aa3999e9be1fa
Source noteuspto-grants-1978_11