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Formamide → 4-Chloroquinazoline
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Formamide | HCID 713 | — |
| 反応物 | Quinazoline | HCID 9210 | — |
| 反応物 | Gold's Reagent | HCID 11008255 | — |
| 反応物 | HCID 178517962 | HCID 178517962 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 生成物 | 4-Chloroquinazoline | HCID 78864 | — |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05411963 |
| 出典データセット | uspto-grants-1995_05 |
| ORD ID | ord-f16f3c2a2f8d4f759a391b79a9ed7598 |
| 出典メモ | uspto-grants-1995_05 |