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HRID 1809645作成日:2026年10月26日

Ammonium formate → 3-(3-Methylpyridazin-4-yloxy)pyridin-2-amine

https://huagongshe.com/reaction/1809645

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium formateHCID 2723923—
反応物3-(6-Chloro-3-methylpyridazin-4-yloxy)pyridin-2-amineHCID 86641108—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
生成物3-(3-Methylpyridazin-4-yloxy)pyridin-2-amineHCID 6748593672%

反応条件

温度65 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US08362037B2
出典データセットuspto-grants-2013_01
ORD IDord-ab8f16fdfeb7404c8cd72867e0bbbefb
出典メモuspto-grants-2013_01