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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 531901Generated: October 29, 2026

2-Aminothiazole → 1,1-Dicyclohexyl-3-thiazol-2-yl-urea

https://huagongshe.com/reaction/531901

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
ReactantDicyclohexylamineHCID 7582—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product1,1-Dicyclohexyl-3-thiazol-2-yl-ureaHCID 11174284—

Reaction Steps

To a solution of aminothiazole (50 mg, 0.5 mmol) in dichloromethane was added carbonyldiimidazole (81 mg, 0.5 mmol) and the solution stirred 2 h at room temperature. Dicyclohexylamine (1 eq) was then added and the reaction stirred overnight at room temperature. The reaction mixture is then diluted with ethyl acetate (8 mL), washed successively with 10% sodiumhydrogensulphate (3 mL), water (3 mL), dried over magnesium sulphate, concentrated in vacuo, and the residue purified by HPLC (Gilson 1, X-terra column; 0-100% CH3CN/H2O/0, 1% TFA; 15 min; flow 50 ml/min) to give the title product (52 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE045183E1
Source datasetuspto-grants-2014_10
ORD IDord-dcf5ebbe7d3e40ecb5e3a5bbd7e135a5
Source noteuspto-grants-2014_10