Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946339Generated: October 31, 2026

Urea → HCID 59547881, compound

https://huagongshe.com/reaction/1946339

Reaction equation

Participants

RoleNameHCIDCharge
ReactantUreaHCID 1176—
ReactantSodium NitriteHCID 23668193—
ReactantHCID 59547994HCID 59547994—
CatalystCopper SulfateHCID 24462—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 59547881HCID 59547881—

Reaction Conditions

Temperature5 °C

Reaction Steps

To a suspension of N-(1-{[5-amino-2-(trifluoromethyl)phenyl]methyl}-1H-pyrazol-3-yl)-2,6-difluorobenzamide (for a preparation see Intermediate 41) (1.0 g, 2.52 mmol) in water (15 ml) in an ice-water bath was added a solution of sodium nitrite (0.346 g, 5.01 mmol, Aldrich) in water (3 ml). The solution was maintained at 0-10° C. for 20 min. To the solution was added urea (0.94 g, 15.65 mmol, Aldrich) and then copper (II) sulphate (0.139 g, 0.868 mmol, Fluka). The mixture was heated to 90° C. for 30 min. The mixture was partitioned between water (150 ml) and ethyl acetate (130 ml). The phases were separated and the aqueous phase washed with ethyl acetate (50 ml). The combined organic extracts were dried (MgSO4), filtered and the solvent removed in vacuo to leave an oil. The residue was loaded in dichloromethane and purified on silica 100 g using a 0-100% ethyl acetate-cyclohexane. The appropriate fractions were combined and evaporated in vacuo to give the title compound as an orange solid (0.462 g); LCMS: (System 4) MH+=398, tRET=2.36 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399436B2
Source datasetuspto-grants-2013_03
ORD IDord-1a9923470de74d1ea241790d6a8d7a03
Source noteuspto-grants-2013_03