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Quinazoline → 2,4-Diamino-5-chloro-6-(5-chloro-2-hydroxyphenyl)quinazoline
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Quinazoline | HCID 9210 | — |
| 反応物 | Boron tribromide | HCID 25134 | — |
| 反応物 | 2,4-Diamino-5-chloro-6-(5-chloro-2-methoxyphenyl)quinazoline | HCID 54072668 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 2,4-Diamino-5-chloro-6-(5-chloro-2-hydroxyphenyl)quinazoline | HCID 54369095 | — |
反応手順
A series of quinazoline analogs may be prepared from the above 2,4-diamino-5-chloro-6-(5-chloro-2-methoxyphenyl)quinazoline. This is accomplished by the reaction of 2,4-diamino-5-chloro-6-(5-chloro-2-methoxyphenyl)quinazoline with 1M boron tribromide in methylene chloride, yielding the corresponding 2,4-diamino-5-chloro-6-(5-chloro-2-hydroxyphenyl)quinazoline. The hydroxy intermediate in turn is reacted with a halogen-containing compound and potassium carbonate in N,N-dimethylformamide, affording the appropriately 6-(5-chloro-2-substituted-phenyl)quinazoline, for example, 2,4-diamino-5-chloro-6-[5-chloro-2-(pyridin-2-ylmethoxy)phenyl]quinazoline. Example 3 describes in detail the preparation of this compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05616718 |
| 出典データセット | uspto-grants-1997_04 |
| ORD ID | ord-7bbc177f69574626b20c30222e1109fd |
| 出典メモ | uspto-grants-1997_04 |