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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127114Generated: October 31, 2026

Potassium Hydroxide → {2-[(Methylcarbamoyl)amino]-1,3-thiazol-4-yl}acetic acid

https://huagongshe.com/reaction/127114

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantEthyl {2-[(methylcarbamoyl)amino]-1,3-thiazol-4-yl}acetateHCID 20288637—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product{2-[(Methylcarbamoyl)amino]-1,3-thiazol-4-yl}acetic acidHCID 2028864585.7%

Reaction Steps

To a solution of ethyl 2-(3-methylureido)thiazol-4-ylacetate (12.8 g.) in a mixture of methanol (240 ml.) and water (240 ml.) was dropwise added 1 N potassium hydroxide aqueous solution (52.7 ml.) with stirring at room temperature, and the solution was stirred for overnight at the same temperature, and then methanol was distilled off therefrom under reduced pressure. The remaining aqueous layer was washed with ethyl acetate, and then 1 N hydrochloric acid (52.7 ml.) was added thereto under ice-cooling. The precipitated crystals were collected by filtration, washed with water and then dried to give colorless crystals of 2-(3-methylureido)thiazol-4-ylacetic acid (9.7 g.), mp 190° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04254260
Source datasetuspto-grants-1981_03
ORD IDord-7a0f1198a66b4233988745ff78fc7b87
Source noteuspto-grants-1981_03