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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903098Generated: October 25, 2026

2-Aminothiazole → 2-cyano-N-(1,3-thiazol-2-yl)acetamide

https://huagongshe.com/reaction/1903098

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
ReactantCyanoacetic acidHCID 9740—
ReactantDicyclohexylcarbodiimideHCID 10868—
SolventAcetonitrileHCID 6342—
SolventSodium HydroxideHCID 14798—
Product2-cyano-N-(1,3-thiazol-2-yl)acetamideHCID 693166—

Reaction Steps

4.5 g of cyanoacetic acid and 5.3 g of 2-aminothiazole, each in acetonitrile were combined, and the suspension (60 ml) was treated with a solution of 12.0 g of dicyclohexylcarbodiimide in 30 ml of acetonitrile. After exothermic reaction (and solidification) additional acetonitrile (60 ml) was added and the mixture stirred 1 hr and let stand overnight. The collected solid (20 g) was stirred with dilute (ca. 2%) NaOH solution and filtered. The filtrate was acidified with 6 N HCl and the product collected, washed with water, dried (m.p. 229°-230°) and recrystallized from acetone to give 2-(cyanoacetylamino)thiazole, m.p. 231°-2° dec.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04435407
Source datasetuspto-grants-1984_03
ORD IDord-7aed9a92fe354bd6b93832256714feb2
Source noteuspto-grants-1984_03