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HRID 35587作成日:2026年10月24日

Pyridine → N-(6-methoxypyridin-3-yl)cyclopropanecarboxamide

https://huagongshe.com/ja/reaction/35587

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物Cyclopropanecarbonyl chlorideHCID 77637—
反応物6-Methoxy-3-pyridinylamineHCID 81121—
溶媒DichloromethaneHCID 6344—
生成物N-(6-methoxypyridin-3-yl)cyclopropanecarboxamideHCID 86308—

反応手順

5-Amino-2-methoxy pyridine (12.4 grams, 0.10 mole) and 10 milliliters (ml) of pyridine were mixed together in 200 ml dichloromethane in a reaction flask. 9.1 ml (0.10 mole) of cyclopropane carboxylic acid chloride was added to the reaction mixture over a period of 2 minutes. The reaction was exothermic and temperature rose to 34° C. The reaction was allowed to stand for one hour at room temperature, after which the reaction mixture was washed with 200 ml of 5% sodium hydroxide and 100 ml water. The resulting organic phase was separated and dried over anhydrous magnesium sulfate. Crystals formed, so the mixture was filtered and washed with 300 ml of acetone and the filtrate evaporated in vacuo to give a solid that was triturated with hexane to yield 16.7 grams, after drying. The product was identified by IR and NMR as the title compound, having a melting point of 130°-131° C. This compound will be referred to as Compound 1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04767771
出典データセットuspto-grants-1988_08
ORD IDord-f066b849c2e2421e9866f1709210e31c
出典メモuspto-grants-1988_08