関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ammonium formate | HCID 2723923 | — |
| 反応物 | 3-(6-Chloro-3-methylpyridazin-4-yloxy)pyridin-2-amine | HCID 86641108 | — |
| 触媒 | Palladium | HCID 23938 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 3-(3-Methylpyridazin-4-yloxy)pyridin-2-amine | HCID 67485936 | 72% |
反応手順
3-(6-Chloro-3-methylpyridazin-4-yloxy)pyridin-2-amine (3.0 g, 12.7 mmol) was charged with MeOH (150 mL). Pd/C (0.67 g, 0.63 mmol) was added followed by ammonium formate (2.23 g, 35.5 mmol). The mixture was heated at 65° C. overnight. The solution was cooled and filtered through GF/F paper. The filtrate was concentrated and the residue was dissolved in dichloromethane and saturated NaHCO3. The organic layer was separated and the aqueous layer was extracted twice with dichloromethane. The combined organics were dried and concentrated to give 3-(3-methylpyridazin-4-yloxy)pyridin-2-amine (1.85 g, 72%) as a solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08362037B2 |
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| 出典データセット | uspto-grants-2013_01 |
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| ORD ID | ord-ab8f16fdfeb7404c8cd72867e0bbbefb |
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| 出典メモ | uspto-grants-2013_01 |
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