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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353652Generated: October 30, 2026

Dimethyl Sulfoxide → 1-[3-tert-Butyl-1-p-tolyl-1H-pyrazol-5-yl]-3-{4-[5-(morpholin-4-ylmethyl)fur-2-yl]naphthalen-1-yl}urea

https://huagongshe.com/reaction/353652

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantDiisopropylethylamineHCID 81531—
Reactant2,2,2-Trichloroethyl 3-tert-butyl-1-P-tolyl-1H-pyrazol-5-ylcarbamateHCID 9931094—
Reactant1-Amino-4-[5-(morpholin-4-ylmethyl)fur-2-yl]naphthaleneHCID 12074207—
SolventEthyl AcetateHCID 8857—
Product1-[3-tert-Butyl-1-p-tolyl-1H-pyrazol-5-yl]-3-{4-[5-(morpholin-4-ylmethyl)fur-2-yl]naphthalen-1-yl}ureaHCID 9937787—

Reaction Steps

A solution of 5-(2,2,2-trichloroethoxycarbonyl)amino-3-t-butyl-1-p-tolylpyrazole (26 mmol), 1-amino-4-[5-(morpholin-4-ylmethyl)fur-2-yl]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 numberUS06753426B2
Source datasetuspto-grants-2004_06
ORD IDord-c2cf5a8b693e452dbf19d3e2ee0ac7cf
Source noteuspto-grants-2004_06