HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1008340Erstellt: 24. Oktober 2026
Chloroform → 4-{[7-(Benzyloxy)-6-methoxy-4-quinazolinyl]oxy}-2-chloroaniline
https://huagongshe.com/de/reaction/1008340
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Chloroform | HCID 6212 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 7-(Benzyloxy)-4-chloro-6-methoxyquinazoline | HCID 10661998 | — |
| Edukt | 4-Amino-3-chlorophenol hydrochloride | HCID 12598190 | — |
| Katalysator | Tetrabutylammonium Chloride | HCID 70681 | — |
| Lösungsmittel | Acetone | HCID 180 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 4-{[7-(Benzyloxy)-6-methoxy-4-quinazolinyl]oxy}-2-chloroaniline | HCID 22667232 | 90% |
Reaktionsschritte
7-(Benzyloxy)-4-chloro-6-methoxyquinazoline (30.0 g) and tetrabutylammonium chloride (13.9 g) were dissolved in acetone (400 ml), and the solution was stirred at room temperature. A solution of 4-amino-3-chlorophenol hydrochloride (36.0 g) in a 20% aqueous sodium hydroxide solution (64 ml) was added thereto. The mixture was then heated under reflux for 3 hr. The reaction solution was cooled to room temperature, and chloroform and water were added to the cooled reaction solution, followed by extraction with chloroform. The extract was washed with a saturated aqueous sodium hydrogencarbonate solution and saturated brine and was then dried over anhydrous sodium sulfate. Next, sodium sulfate was removed, and the solvent was then removed by distillation. The residue was washed with methanol, and the washed solid was subjected to evaporation to dryness in vacuo through a vacuum pump to give 36.6 g (yield 90%) of the title compound.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06797823B1 |
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| Quelldatensatz | uspto-grants-2004_09 |
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| ORD ID | ord-2f79078892f0406ba85cbcd90b3c5a14 |
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| Quellennotiz | uspto-grants-2004_09 |
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