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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 499203Generated: October 30, 2026

Benzoic Acid → 1-(5-tert-Butyl-2-methyl-2H-pyrazol-3-yl)-3-{4-[1-(benzoyl)-piperidin-4-yloxy]phenyl}urea

https://huagongshe.com/reaction/499203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoic AcidHCID 243—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1-(5-tert-Butyl-2-methyl-2H-pyrazol-3-yl)-3-[4-(piperidin-4-yloxy)-phenyl]-ureaHCID 59420883—
SolventTetrahydrofurane dichloromethaneHCID 21919333—
Product1-(5-tert-Butyl-2-methyl-2H-pyrazol-3-yl)-3-{4-[1-(benzoyl)-piperidin-4-yloxy]phenyl}ureaHCID 5942088093.4%

Reaction Conditions

Temperature22 °C

Reaction Steps

To an ice-cooled solution of 1-(5-tert-butyl-2-methyl-2H-pyrazol-3-yl)-3-[4-(piperidin-4-yloxy)-phenyl]-urea (82.2 mg, 0.22 mmol), 1-hydroxybenzotriazole (HOBt, 50.1 mg, 0.37 mmol), and benzoic acid (38.8 mg, 0.32 mmol) in dichloromethane-THF (1:1, 2 mL) is added DCC (52.0 mg, 0.25 mmol). The reaction mixture is stirred at 22° C. for 19 hours. The crude product is purified on a silica gel chromatography with ethyl acetate-hexanes to provide a white solid (97.7 mg, 93.4% yield, ES+(m/z) 476.1 [M+H]).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07767674B2
Source datasetuspto-grants-2010_08
ORD IDord-834d296d488442fdaeb9f1d45c2a54c2
Source noteuspto-grants-2010_08