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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35834Generated: October 26, 2026

Formamide → 4-Chloroquinazoline

https://huagongshe.com/reaction/35834

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormamideHCID 713—
ReactantQuinazolineHCID 9210—
ReactantGold's ReagentHCID 11008255—
ReactantHCID 178517962HCID 178517962—
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. 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05411963
Source datasetuspto-grants-1995_05
ORD IDord-f16f3c2a2f8d4f759a391b79a9ed7598
Source noteuspto-grants-1995_05