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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 31548생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/31548

반응식

참여 물질

역할이름HCID투입량
반응물Citric AcidHCID 311—
반응물TriethylamineHCID 8471—
반응물1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
반응물5-Methoxyindole-2-carboxylic acidHCID 20401—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물Methanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물N,5-Dimethoxy-N-methyl-1H-indole-2-carboxamideHCID 2300332673.9%

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07425642B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-7b23b6dc3dc64421a1c074c6a21315e7
출처 메모uspto-grants-2008_09