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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387992Generated: October 28, 2026

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

https://huagongshe.com/reaction/387992

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 saline 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 numberUS08372981B2
Source datasetuspto-grants-2013_02
ORD IDord-9ff303bd2a324f929b117d27380c3ab3
Source noteuspto-grants-2013_02