HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 16405Erstellt: 24. Oktober 2026
Potassium Hydroxide → 4-((1H-Pyrrolo[2,3-B]pyridin-4-YL)oxy)-3-fluoroaniline
https://huagongshe.com/de/reaction/16405
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Edukt | Phenol, 4-amino-2-fluoro- | HCID 2735918 | — |
| Edukt | 4-Chloro-1H-pyrrolo[2,3-b]pyridine | HCID 11389493 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 4-((1H-Pyrrolo[2,3-B]pyridin-4-YL)oxy)-3-fluoroaniline | HCID 16037965 | — |
Reaktionsschritte
543 mg (3.56 mmol) of 4-chloro-1H-pyrrolo[2,3-b]pyridine (from example XVIII, 905 mg (7.12 mmol) of 3-fluoro-4-hydroxyaniline and 399 mg (7.12 mmol) of powdered potassium hydroxide are heated at 260° C. for 8 hours. Another 905 mg (7.12 mmol) of 3-fluoro-4-hydroxyaniline and 200 mg (3.56 mmol) of powdered potassium hydroxide are added, and the mixture is reacted at 260° C. for another 8 h. For work-up, the mixture is cooled to room temperature, diluted with water and extracted three times with ethyl acetate. The organic phase is dried over magnesium sulfate and concentrated using a rotary evaporator. The residue is purified by preparative HPLC. The fractions which, according to LC-MS, contain 39% of product are used without further purification for the next reaction.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07737153B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-e1ae06632b2441b793d7925135e5427b |
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| Quellennotiz | uspto-grants-2010_06 |
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