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Hydrochloric Acid → N-{4-[(3-Amino-1,2-benzisoxazol-4-yl)oxy]-3-fluorophenyl}-N-[2-amino-6-(4-pyridinyl)-4-pyrimidinyl]amine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | 4-(4-Amino-2-fluorophenoxy)-1,2-benzisoxazole-3-amine | HCID 17979297 | — |
| 反応物 | 4-Chloro-6-(pyridin-4-yl)pyrimidin-2-amine | HCID 22324286 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | N-{4-[(3-Amino-1,2-benzisoxazol-4-yl)oxy]-3-fluorophenyl}-N-[2-amino-6-(4-pyridinyl)-4-pyrimidinyl]amine | HCID 17979269 | — |
反応手順
70 mg (0.27 mmol) of 4-(4-amino-2-fluorophenoxy)-1,2-benzisoxazole-3-amine (from example VII) and 55.8 mg (0.27 mmol) of 4-chloro-6-(4-pyridinyl)-2-pyrimidineamine (from example XXIX) are suspended in 4 ml of water, and 0.02 ml of concentrated hydrochloric acid is added. The reaction mixture is heated at reflux overnight, resulting in the formation of a lightly colored precipitate. This is filtered off, washed repeatedly with water and dried under high vacuum.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07737153B2 |
| 出典データセット | uspto-grants-2010_06 |
| ORD ID | ord-61b7c47c928949d9baad30b4fe9e65b1 |
| 出典メモ | uspto-grants-2010_06 |