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HRID 53443作成日:2026年10月24日

Pyridine → 2-Valerylamino-5-bromo-4-methyl-3-nitropyridine

https://huagongshe.com/ja/reaction/53443

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物DichloromethaneHCID 6344—
反応物Valeryl chlorideHCID 61186—
反応物2-Amino-5-bromo-4-methyl-3-nitropyridineHCID 7213207—
溶媒WaterHCID 962—
生成物2-Valerylamino-5-bromo-4-methyl-3-nitropyridineHCID 2146417381%

反応条件

温度110 °C

反応手順

A mixture comprising 10 g (43.1 mmol) of 2-amino-5-bromo-4-methyl-3-nitropyridine and 6.8 g of pyridine was heated to 110° C. in a nitrogen atmosphere. 5.7 g (47.4 mmol) of valeroyl chloride was dropwise added thereto and the mixture was stirred at 110° C. for 5 hours. The reaction mixture was brought to room temperature, followed by the addition of methylene chloride (50 ml) and water (50 ml). The organic phase was separated. The aqueous phase was further extracted with methylene chloride (50 ml). The organic phases were combined, dried over anhydrous magnesium sulfate and subjected to vacuum concentration to give a crude crystal. It was recrystallized from ethyl acetate to give 11 g of 2-valerylamino-5-bromo-4-methyl-3-nitropyridine (yield 81%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05618969
出典データセットuspto-grants-1997_04
ORD IDord-1da1f522f51f4cdfa04c306c6fee3dc0
出典メモuspto-grants-1997_04