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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1370749Generated: October 25, 2026

Dimethyl Sulfoxide → 1-[3-tert-butyl-1-(2-methylpyridin-5-yl)-1H-pyrazol-5-yl]-3-[4-(pyridin-4-yl-methoxy)naphthalen-1-yl]-urea

https://huagongshe.com/reaction/1370749

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantDiisopropylethylamineHCID 81531—
Reactant5-(2,2,2-Trichloroethoxycarbonyl)amino-3-t-butyl-1-(2-methylpyridin-5-yl)pyrazoleHCID 12988816—
Reactant4-(4-Pyridinylmethoxy)-1-naphthalenamineHCID 15908535—
SolventEthyl AcetateHCID 8857—
Product1-[3-tert-butyl-1-(2-methylpyridin-5-yl)-1H-pyrazol-5-yl]-3-[4-(pyridin-4-yl-methoxy)naphthalen-1-yl]-ureaHCID 9957853—

Reaction Steps

A solution of 5-(2,2,2-trichloroethoxycarbonyl)amino-3-t-butyl-1-(2-methylpyridin-5-yl)pyrazole (26 mmol), 1-amino-4-(pyridin-4-ylmethoxy)naphthalene (26 mmol), diisopropylethylamine (25 mmol) and DMSO (75 mL) is heated to 55-90° C. and held for 2-8 h. To this solution, ethyl acetate (100 mL) is added. The organic layer is washed with brine (4×50 mL), and dried over MgSO4. The solvent is removed under reduced pressure, and residue is crystallized from a suitable solvent such as acetonitrile (50 mL) at 0° C. The product is collected by filtration and recrystallized from a suitable solvent such as isopropanol and dried in vacuum to constant weight.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06583282B1
Source datasetuspto-grants-2003_06
ORD IDord-6c0e0189e37b4da991746dbacc751b88
Source noteuspto-grants-2003_06