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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433650Generated: October 30, 2026

Water → N-(3-Methylsulfonylphenyl)-N'-(4-(6-phenylaminopyrimidin-4-yloxy)phenyl)urea

https://huagongshe.com/reaction/1433650

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPhenyl 3-methylsulfonylphenylcarbamateHCID 22936234—
ReactantN-(6-(4-Aminophenoxy)pyrimidin-4-yl)phenylamineHCID 22936405—
SolventDimethyl SulfoxideHCID 679—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
ProductN-(3-Methylsulfonylphenyl)-N'-(4-(6-phenylaminopyrimidin-4-yloxy)phenyl)ureaHCID 2293624681%

Reaction Steps

N-(6-(4-Aminophenoxy)pyrimidin-4-yl)phenylamine (55.6 mg, 0.200 mmol) and (3-methylsulfonylphenyl)carbamic acid phenyl ester (63.8 mg, 0.220 mmol) were heated and stirred in dimethylsulfoxide (1 ml) at 85° C. for 2 hours. The reaction solution was distributed between ethyl acetate and water, the organic layer was washed with 1N aqueous sodium hydroxide, water and saturated brine and dried over anhydrous magnesium sulfate, the drying agent was filtered off and the filtrate was distilled off under reduced pressure. The obtained crude product was suspended in ethyl acetate, the suspension was diluted with hexane, and the crystals were filtered out, washed with hexane and then blow-dried to obtain the title compound (77.0 mg, 0.162 mmol, 81%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612092B2
Source datasetuspto-grants-2009_11
ORD IDord-840a2ee7bd79400f84052adda78e1d04
Source noteuspto-grants-2009_11