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HRID 31548作成日:2026年10月26日

Citric Acid → N,5-Dimethoxy-N-methyl-1H-indole-2-carboxamide

https://huagongshe.com/reaction/31548

反応式

関与物質

役割名称HCID仕込み量
反応物Citric AcidHCID 311—
反応物TriethylamineHCID 8471—
反応物1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
反応物5-Methoxyindole-2-carboxylic acidHCID 20401—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物Methanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物N,5-Dimethoxy-N-methyl-1H-indole-2-carboxamideHCID 2300332673.9%

反応手順

To a solution of 5-methoxyindole-2-carboxylic acid (5 g, 26 mmol) in N,N-dimethylformamide were added N,O-dimethylhydroxyamine hydrochloride (3.04 g, 31.2 mmol) and WSC (5.98 g, 31.2 mmol), 1-hydroxybenzotriazole (4.21 g, 31.2 mmol) and triethylamine (7.24 ml, 52 mmol), and the mixture was stirred for 6 hours. To this reaction solution were added ethyl acetate and 10% (Wt) citric acid, and the organic layer was extracted. The aqueous layer was extracted twice with ethyl acetate, and combined with the organic layer. The mixture was washed with a saturated aqueous sodium hydrogen carbonate solution and saturated saline. The organic layer was separated, and dried over anhydrous sodium sulfate, filtered, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=4:1) to give the title compound (4.5 g, 70%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07425642B2
出典データセットuspto-grants-2008_09
ORD IDord-7b23b6dc3dc64421a1c074c6a21315e7
出典メモuspto-grants-2008_09