HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formamide → 4-Chloroquinazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formamide | HCID 713 | — |
| Reactant | Quinazoline | HCID 9210 | — |
| Reactant | Gold's Reagent | HCID 11008255 | — |
| Reactant | HCID 178517962 | HCID 178517962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-Chloroquinazoline | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05411963 |
| Source dataset | uspto-grants-1995_05 |
| ORD ID | ord-f16f3c2a2f8d4f759a391b79a9ed7598 |
| Source note | uspto-grants-1995_05 |