HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 81656Erstellt: 24. Oktober 2026
Ammonium Chloride → 6-{[3-chloro-5-(2,2-diethoxyethoxy)pyridin-2-yl]oxy}-N-pyrazin-2-ylquinazoline-4-amine
https://huagongshe.com/de/reaction/81656
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | Potassium tert-butoxide | HCID 23665647 | — |
| Edukt | 2,3-Dichloro-5-(2,2-diethoxyethoxy)pyridine | HCID 86645896 | — |
| Edukt | 4-(Pyrazin-2-ylamino)quinazolin-6-ol | HCID 136334744 | — |
| Lösungsmittel | Dimethylacetamide | HCID 31374 | — |
| Produkt | 6-{[3-chloro-5-(2,2-diethoxyethoxy)pyridin-2-yl]oxy}-N-pyrazin-2-ylquinazoline-4-amine | HCID 68430657 | 10% |
Reaktionsschritte
2,3-Dichloro-5-(2,2-diethoxyethoxy)pyridine (810 mg, 2.9 mmol) and potassium tert-butoxide (350 mg, 3.1 mmol) were added to an N,N-dimethylacetamide suspension (3 ml) of 4-(pyrazin-2-ylamino)quinazolin-6-ol (300 mg, 1.25 mmol), and stirred for 24 hours in a sealed tube at 200° C. The reaction solution was cooled to room temperature, aqueous saturated ammonium chloride solution was added, filtered, and washed with a mixed solution of chloroform/methanol (9:1). The obtained filtrate was extracted with chloroform, the organic layer was washed with water and saturated saline water, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The obtained residue was purified by reversed-phase liquid chromatography (YMC CombiPrep Pro C18 AS-360-cc) to obtain 6-{[3-chloro-5-(2,2-diethoxyethoxy)pyridin-2-yl]oxy}-N-pyrazin-2-ylquinazoline-4-amine (60 mg, yield: 10%) as a pale yellow solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08846700B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-c6a64b49652946daa6df266cc8c90601 |
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| Quellennotiz | uspto-grants-2014_09 |
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