HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1993348Erstellt: 25. Oktober 2026
4-Fluoroaniline → 5-(3-fluoro-4-hydroxyphenyl)-2-(4-fluorophenylamino)-3-methylpyrimidin-4(3H)-one
https://huagongshe.com/reaction/1993348
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4-Fluoroaniline | HCID 9731 | — |
| Edukt | 5-(3-fluoro-4-hydroxyphenyl)-3-methyl-2-methylthio-3H-pyrimidin-4-one | HCID 68420610 | — |
| Katalysator | Hydrochloric Acid | HCID 313 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 5-(3-fluoro-4-hydroxyphenyl)-2-(4-fluorophenylamino)-3-methylpyrimidin-4(3H)-one | HCID 68418594 | — |
Reaktionsschritte
5-(3-Fluoro-4-hydroxyphenyl)-3-methyl-2-methylthio-3H-pyrimidin-4-one (Step 5, 0.39 g, 1.5 mmol) was suspended in 3.6 mL p-fluoroaniline and concentrated HCl (1 drop) was added. The reaction was heated in a microwave at 120° C. and 100 W for 10 min (using a Powermax feature on a CEM microwave). The reaction was cooled to RT and diluted with EtOAc (100 mL). The organic phase was extracted with 1 N NaOH (3×15 mL), and the aqueous extracts were neutralized with concentrated HCl. The aqueous layer was extracted with EtOAc (3×20 mL), and the organic extracts were combined, dried over Na2SO4, filtered, and concentrated to give desired compound. MS (ESI pos. ion) m/z: 330. Calc'd for C17H13F2N3O2: 329.10.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07652009B2 |
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| Quelldatensatz | uspto-grants-2010_01 |
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| ORD ID | ord-721a86c2602a43f19cb1980402827f2e |
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| Quellennotiz | uspto-grants-2010_01 |
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