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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1824447Generated: October 31, 2026

Phosgene → HCID 10218444, compound

https://huagongshe.com/reaction/1824447

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosgeneHCID 6371—
ReactantIsocyanateHCID 105034—
ReactantSodium BicarbonateHCID 516892—
Reactant3-tert-butyl-1-(4-methylphenyl)-1H-pyrazol-5-amineHCID 2974132—
ReactantHCID 22147192HCID 22147192—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10218444HCID 1021844440%

Reaction Conditions

Temperature0 °C

Reaction Steps

3-Amino-5-tert-butyl-2-(p-tolyl)-2H-pyrazole (2.39 g, 9.00 mmol, 1 equiv.) was dissolved in 35 mL methylene chloride and 35 mL saturated aqueous NaHCO3 was added. The biphasic mixture was stirred until all solids had completely dissolved and was then cooled to 0° C. The organic layer was then treated with phosgene in one portion via syringe while not stirring (15.8 mL of a 20% solution toluene, 31.5 mmol, 3.5 equiv.). The resulting mixture was stirred vigorously at 0° C. for 1 h. The organic layer was separated, dried (Na2SO4) and filtered. The methylene chloride was removed in vacuo and the resulting isocyanate in toluene was treated with a solution of aminonaphthyl-chloropyrimidyl ether intermediate (see Example 4) (2.45 g, 9.0 mmol, 1.0 equiv.) in 40 mL anhydrous THF. The mixture was stirred at room temperature for 3.5 h, then the solvent was removed in vacuo. The residue was purified by column chromatography on silica gel using 0–10% MeOH in methylene chloride eluent mixtures, followed by recrystallization from ether, providing 1.90 g (40%) of the urea intermediate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07041669B2
Source datasetuspto-grants-2006_05
ORD IDord-8af70fdf728d4e61b923bd1cea7bdff6
Source noteuspto-grants-2006_05