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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 487577Erstellt: 25. Oktober 2026

Formamide → 4-Chloroquinazoline

https://huagongshe.com/reaction/487577

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFormamideHCID 713—
EduktQuinazolineHCID 9210—
EduktPhosphorus pentachlorideHCID 24819—
EduktGold's ReagentHCID 11008255—
EduktHCID 178517962HCID 178517962—
LösungsmittelPhosphorus oxychlorideHCID 24813—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt4-ChloroquinazolineHCID 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. Gupton; Correia, K.; Hertel, G. Synthetic Communications, 1984, 14, 1013). Once in hand, the 4-hydroxy quinazoline is chlorinated under standard conditions, using for example phosphorus pentachloride in phosphorus oxychloride, to provide 4-chloroquinazoline starting materials. The 4-hydroxy quinazoline derivatives can advantageously be chlorinated using the chlorinating reagents and procedure disclosed in U.S. Pat. No. 4,230,644.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05296484
Quelldatensatzuspto-grants-1994_03
ORD IDord-6a3211e780de4b41a12fb9630be8eae3
Quellennotizuspto-grants-1994_03