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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 3-Aminophenol | HCID 11568 | — |
| Reactant | 2-Chloro-5-(4-(difluoromethoxy)phenyl)pyrimidine | HCID 58171930 | — |
| Solvent | Sodium Carbonate | HCID 10340 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-(5-(4-(Difluoromethoxy)phenyl)pyrimidin-2-ylamino)phenol | HCID 68729559 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08293757B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-6a43c11cef454addb94ccd7738b48468 |
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| Source note | uspto-grants-2012_10 |
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