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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1799669Generated: October 27, 2026

Ethyl 2-aminothiazole-4-carboxylate → Ethyl 2-amino-5-iodo-1,3-thiazole-4-carboxylate

https://huagongshe.com/reaction/1799669

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-aminothiazole-4-carboxylateHCID 73216—
ReactantN-IodosuccinimideHCID 120273—
SolventTetrahydrofuranHCID 8028—
SolventSodium chloride; waterHCID 57417360—
ProductEthyl 2-amino-5-iodo-1,3-thiazole-4-carboxylateHCID 4511758884%

Reaction Steps

A solution of 14.53 g of 2-amino-4-ethoxycarbonylthiazole in 200 ml of THF was cooled in ice under an argon atmosphere, 20.0 g of N-iodosuccinimide was added to the cooled solution, and the mixture was stirred at the same temperature for 1.5 hr. Brine was added to the reaction solution, and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, was filtered, and was concentrated under the reduced pressure. The residue was purified by column chromatography on silica gel (hexane:ethyl acetate=1:1 to 1:2) to give 21.12 g of 2-amino-4-ethoxycarbonyl-5-iodothiazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08344154B2
Source datasetuspto-grants-2013_01
ORD IDord-b38b169995ae4315973a4b8575b25c57
Source noteuspto-grants-2013_01