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Dimethylamine tetrahydrofuran → 6-({3-chloro-5-[2-(dimethylamino)ethoxy]pyridin-2-yl}oxy)-N-(5-methylpyrazin-2-yl)quinazoline-4-amine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dimethylamine tetrahydrofuran | HCID 22320367 | — |
| 反応物 | 3-Chloro-5-(2,2-diethoxyethoxy)-2-fluoropyridine | HCID 68427602 | — |
| 反応物 | 4-((5-Methylpyrazin-2-yl)amino)quinazolin-6-ol | HCID 135618222 | — |
| 生成物 | 6-({3-chloro-5-[2-(dimethylamino)ethoxy]pyridin-2-yl}oxy)-N-(5-methylpyrazin-2-yl)quinazoline-4-amine | HCID 59508867 | — |
反応手順
Using 4-[(5-methylpyrazin-2-yl)amino]quinazolin-6-ol, 3-chloro-5-(2,2-diethoxyethoxy)-2-fluoropyridine and 2 M dimethylamine/tetrahydrofuran solution, and in the same manner as in Example 32 or according to a method similar to it or according to a combination thereof with an ordinary method, the entitled compound (14 mg) was obtained as a pale yellow amorphous solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08846700B2 |
| 出典データセット | uspto-grants-2014_09 |
| ORD ID | ord-5b3fb5f4479042eba32fefa1955e7f91 |
| 出典メモ | uspto-grants-2014_09 |