HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 634732Erstellt: 25. Oktober 2026
Hydrochloric Acid → 4-(2-Fluoro-5-hydroxy-4-methylanilino)-7-(3-morpholinopropionamido)quinazoline
https://huagongshe.com/reaction/634732
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 4-(2-Fluoro-5-methoxycarbonyloxy-4-methylanilino)-7-(3-morpholinopropionamido)quinazoline | HCID 21260355 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 4-(2-Fluoro-5-hydroxy-4-methylanilino)-7-(3-morpholinopropionamido)quinazoline | HCID 21260319 | 80% |
Reaktionsschritte
2M Aqueous sodium hydroxide solution (453 μl, 0.9 mmol) was added to a suspension of 4-(2-fluoro-5-methoxycarbonyloxy-4-methylanilino)-7-(3-morpholinopropionamido)quinazoline (219 mg, 0.45 mmol) in methanol (6 ml) and the mixture stirred for 1 hour. The reaction mixture was diluted with water and then adjusted to pH6 with 2M hydrochloric acid. The resulting precipitate was collected by filtration, washed with water and ethanol, and dried. The solid was dissolved in methylene chloride/methanol and a 5M solution of hydrogen chloride in isopropanol (0.3 ml) added. The volatiles were removed by evaporation, the resulting solid was washed with ether, and dried under vacuum to give 4-(2-fluoro-5-hydroxy-4-methylanilino)-7-(3-morpholinopropionamido)quinazoline (1-86 mg, 80%) as a yellow solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06184225B2 |
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| Quelldatensatz | uspto-grants-2001_02 |
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| ORD ID | ord-acf00f39016b4701a3e228fcd490f95f |
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| Quellennotiz | uspto-grants-2001_02 |
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