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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 487577Generated: October 24, 2026

Formamide → 4-Chloroquinazoline

https://huagongshe.com/en/reaction/487577

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormamideHCID 713—
ReactantQuinazolineHCID 9210—
ReactantPhosphorus pentachlorideHCID 24819—
ReactantGold's ReagentHCID 11008255—
ReactantHCID 178517962HCID 178517962—
SolventPhosphorus oxychlorideHCID 24813—
Solvent1,4-DioxaneHCID 31275—
Product4-ChloroquinazolineHCID 78864—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05296484
Source datasetuspto-grants-1994_03
ORD IDord-6a3211e780de4b41a12fb9630be8eae3
Source noteuspto-grants-1994_03