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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2067898Generated: October 26, 2026

p-Toluenesulfonic acid → 3-(5-(4-(Difluoromethoxy)phenyl)pyrimidin-2-ylamino)phenol

https://huagongshe.com/reaction/2067898

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant3-AminophenolHCID 11568—
Reactant2-Chloro-5-(4-(difluoromethoxy)phenyl)pyrimidineHCID 58171930—
SolventSodium CarbonateHCID 10340—
Solvent1,4-DioxaneHCID 31275—
Product3-(5-(4-(Difluoromethoxy)phenyl)pyrimidin-2-ylamino)phenolHCID 68729559—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a mixture of 2-chloro-5-(4-(difluoromethoxy)phenyl)pyrimidine 30 (3.2 mmol) and 3-aminophenol (6.42 mmol) in 1,4-dioxane (5 mL) is added p-TSA (5.4 mmol). The reaction mixture is heated at 100° C. for 12 h. After this time, the reaction is diluted with a 2M solution of Na2CO3 and extracted with DCM (3×50 mL). The organic layer is washed with brine, dried over Na2SO4, and concentrated. Purification by short SiO2 chromatography using a DCM:EtOAc=7:3 as eluant affords (3-(5-(4-(difluoromethoxy)phenyl)pyrimidin-2-ylamino)phenol 39. MS (m/z) (M+1)+: 330.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293757B2
Source datasetuspto-grants-2012_10
ORD IDord-6a43c11cef454addb94ccd7738b48468
Source noteuspto-grants-2012_10