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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2384142Generated: October 29, 2026

Water → 1,1-Dicyclohexyl-3-[4-methyl-5-(4-methyl-piperazine-1-sulfonyl)-thiazol-2-yl]-urea

https://huagongshe.com/reaction/2384142

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDicyclohexylamineHCID 7582—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant4-Methyl-5-(4-methyl-piperazine-1-sulfonyl)-thiazol-2-ylamineHCID 63946172—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Solvent1,1-DichloroethaneHCID 6365—
Product1,1-Dicyclohexyl-3-[4-methyl-5-(4-methyl-piperazine-1-sulfonyl)-thiazol-2-yl]-ureaHCID 57883646123.2%

Reaction Conditions

Temperature120 °C

Reaction Steps

Prepared in the microwave oven (EmrysOptimizer®). 4-Methyl-5-(4-methyl-piperazine-1-sulfonyl)-thiazol-2-ylamine (0.04 g; 0.141 mmol), CDI (0.023 g; 0.141 mmol) and DMAP were mixed dichloroethane (1.5 ml) in a microwave vessel (2.5 ml). The reaction mixture was heated 600 sec at 120° C., dicyclohexylamine (0.025 g; 0.141 mmol) dissolved in dichloroethane (0.2 ml) was added through the septum and the reaction mixture was heated for additional 600 sec. at 120° C. To the reaction mixture was added water and DCM (25 ml). The water phase was extracted with DCM (3×25 ml), dried with MgSO4 filtered and evaporated in vacuo to afford the title compound, (84 mg) as a yellow oil. Purification by prep. HPLC gave 3 mg (Yield: 4%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263634B2
Source datasetuspto-grants-2012_09
ORD IDord-7d3c7f1ee61c4af0b42e7204b330d77f
Source noteuspto-grants-2012_09