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HRID 552145作成日:2026年10月24日

Dimethylformamide → 6-chloro-N-(3-methylbutyl)pyridazine-3-carboxamide

https://huagongshe.com/ja/reaction/552145

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物IsoamylamineHCID 7894—
反応物Thionyl ChlorideHCID 24386—
反応物6-Hydroxy-3-pyridazinecarboxylic acid monohydrateHCID 2774651—
溶媒ChloroformHCID 6212—
溶媒DichloromethaneHCID 6344—
溶媒TriethylamineHCID 8471—
生成物6-chloro-N-(3-methylbutyl)pyridazine-3-carboxamideHCID 16733786—

反応手順

The mixture of 6-oxo-1,6-dihydropyridazine-3-carboxylic acid monohydrate (3.16 g, 20.0 mmol), dimethylformamide (0.5 mL) and thionyl chloride (5-7 mL) in chloroform (70 mL) was kept at 50-60° C. overnight. The reaction mixture was evaporated in vacuo to dryness. The solid residue was dissolved in dichloromethane (70 mL) and added dropwise to the mixture of 3-methylbutylamine (30 mmol, 2.7 mL) and triethylamine (5 mL) in dichloromethane (150 mL) at ambient temperature. The mixture was stirred for 30 min, washed sequentially with 10% HCl solution, saturated NaHCO3 and water, and then dried over MgSO4. The final compound was isolated by recrystallization from ether:hexanes (5:1) (19.76 mmol). Yield: 4.5 g (19.76 mmol), 98%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07951805B2
出典データセットuspto-grants-2011_05
ORD IDord-725dfb35947049579a21d1c7b365355a
出典メモuspto-grants-2011_05