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HRID 40324作成日:2026年10月24日

Oxalyl chloride → N-Methoxy-N-methylquinoline-6-carboxamide

https://huagongshe.com/ja/reaction/40324

反応式

関与物質

役割名称HCID仕込み量
反応物Oxalyl chlorideHCID 65578—
反応物Methanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
反応物DiisopropylethylamineHCID 81531—
反応物6-Quinolinecarboxylic acidHCID 82571—
触媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物N-Methoxy-N-methylquinoline-6-carboxamideHCID 5521117295.2%

反応手順

A 250 mL RB flask was charged with quinoline-6-carboxylic acid (5.00 g, 28.9 mmol), DCM (100 ml, 1554 mmol), oxalyl chloride (3.79 ml, 43.3 mmol), and a few drops of DMF and stirred at RT for 2 hours, then concentrated. The residue was taken up in DCM (100 ml, 1554 mmol), cooled to 0° C., then Hunig's Base (17.7 ml, 101 mmol) and N-methoxymethanamine hydrochloride (2.96 g, 30.3 mmol) were added slowly. The mixture was stirred at room temperature for 16 hours (91463-3-1). The mixture was diluted with DCM (200 mL), then washed with water (250 mL), sat. NaHCO3 (250 mL), and brine (250 mL). The organic layer was dried with MgSO4, filtered, and concentrated to give a brown oil, which was purified by MPLC eluting with 2-6% MeOH/DCM to give N-methoxy-N-methylquinoline-6-carboxamide (5.943 g, 95.2% yield) as a brown oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524900B2
出典データセットuspto-grants-2013_09
ORD IDord-1c22e723dddd4c25b16eeb5f4c0677ad
出典メモuspto-grants-2013_09