関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sodium Carbonate | HCID 10340 | — |
| 反応物 | Tri-tert-butylphosphine tetrafluoroborate | HCID 2734635 | — |
| 反応物 | 2-Fluoropyridine-4-boronic acid | HCID 2783396 | — |
| 反応物 | N-(4-(3-bromopyridin-4-yloxy)phenyl)-4-phenylphthalazin-1-amine | HCID 66731439 | — |
| 触媒 | palladium(II) acetate | HCID 167845 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 生成物 | N-(4-(3-bromopyridin-4-yloxy)phenyl)-4-phenylphthalazin-1-amine | HCID 66731439 | — |
| 生成物 | N-(4-(3-(2-fluoropyridin-4-yl)pyridin-4-yloxy)phenyl)-4-phenylphthalazin-1-amine | HCID 66732281 | — |
反応手順
A resealable reaction tube was charged with tri-tert-butylphosphonium tetrafluoroborate (0.024 g, 0.082 mmol), palladium (II) acetate (0.009 g, 0.041 mmol), 2-fluoropyridine4-boronic acid (0.086 g, 0.614 mmol) and N-(4-(3-bromopyridin4-yloxy)phenyl)-4-phenylphthalazin-1-amine (0.192 mg, 0.409 mmol) and was purged with nitrogen for several minutes. 1.2 mL of dioxane and 2.0 M aqueous sodium carbonate (0.614 mL, 0.123 mmol) were added, the tube was sealed, and the reaction mixture was heated to 100° C. for 48 h. The mixture was diluted with EtOAc and washed with water. The organic portion was dried with MgSO4 and concentrated. Purification by Gilson reverse phase liquid chromatography (5-70% ACN/water/0.1% TFA over 14 min) provided N-(4-(3-(2-fluoropyridin-4-yl)pyridin-4-yloxy)phenyl)-4-phenylphthalazin-1-amine as a mixture with the hydrodehalogenation product of N-(4-(3-bromopyridin-4-yloxy)phenyl)4-phenylphthalazin-1-amine.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07560551B2 |
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| 出典データセット | uspto-grants-2009_07 |
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| ORD ID | ord-bfaff0fbea714597b399ff08fb409554 |
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| 出典メモ | uspto-grants-2009_07 |
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