HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Formamide → 4-Chloroquinazoline
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Formamide | HCID 713 | — |
| Edukt | Quinazoline | HCID 9210 | — |
| Edukt | Gold's Reagent | HCID 11008255 | — |
| Edukt | HCID 178517962 | HCID 178517962 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | 4-Chloroquinazoline | HCID 78864 | — |
Reaktionsschritte
Quinazoline starting materials are commercially available or readily prepared using conventional procedures. For example, 4-hydroxy quinazolines can be prepared from commercially available anthranilic acids via condensation with excess formamide at reflux (M. Endicott et al. J. Am. Chem. Soc., 1946, 68, 1299). Alternatively hydroxy quinazolines can be prepared in dioxane at reflux using Gold's reagent (J. Gipton; Correia, K.; Hertel, G. Synthetic Communications, 1984, 14, 1013). Once in hand, the 4-hydroxy quinazoline is chlorinated under standard conditions to provide 4-chloroquinazoline starting materials.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05411963 |
| Quelldatensatz | uspto-grants-1995_05 |
| ORD ID | ord-f16f3c2a2f8d4f759a391b79a9ed7598 |
| Quellennotiz | uspto-grants-1995_05 |