HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1993354Generated: November 1, 2026
Thiophenol → 2-Fluoro-4-(2-(phenylamino)pyrimidin-5-yl)phenol
https://huagongshe.com/reaction/1993354
Participants
| Role | Name | HCID | Charge |
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| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-(3-fluoro-4-methoxyphenyl)-N-phenylpyrimidin-2-amine | HCID 57445393 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 2-Fluoro-4-(2-(phenylamino)pyrimidin-5-yl)phenol | HCID 57445394 | — |
Reaction Steps
A mixture of 5-(3-fluoro-4-methoxyphenyl)-N-phenylpyrimidin-2-amine (Step 2, 0.066 g, 0.22 mmol), thiophenol (0.20 g, 1.0 mmol), and K2CO3 (0.15 g, 1.1 mmol) in NMP (2 mL) was heated at 120° C. for 20 h. The mixture was cooled to RT and diluted with H2O (4 mL). After stirring for 10 min, the resulting suspension was filtered, and the solid was further washed with H2O. The solid was washed with hexanes to provide the title compound as a brown solid. MS (ESI pos. ion) m/z: 282. Calc'd for C16H12FN3O: 281.10.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07652009B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-b925e905939943bda3fa52233e6c9381 |
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| Source note | uspto-grants-2010_01 |
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