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HRID 53563作成日:2026年10月23日

Indole-3-Butyric Acid → N-Methyl-N-Methoxy-4-(3-indolyl)butyramide

https://huagongshe.com/ja/reaction/53563

反応式

関与物質

役割名称HCID仕込み量
反応物Indole-3-Butyric AcidHCID 8617—
反応物N,N-dimethylhydroxylamine hydrochlorideHCID 27969—
反応物DiisopropylethylamineHCID 81531—
反応物Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
溶媒AcetonitrileHCID 6342—
生成物N-Methyl-N-Methoxy-4-(3-indolyl)butyramideHCID 1110763194.3%

反応手順

To a slurry of 1.75 g (8.61 mmol) of 3-indolebutyric acid (Aldrich Chemical Co.) in acetonitrile at room temperature was added 7.0 mL (40.2 mmol) of N,N-diisopropylethylamine, 1.0 g (10.3 mmol) of N,N-dimethylhydroxylamine hydrochloride and 4.19 g (9.5 mmol) of benzotriazol-1-yloxytris(dimethylamino)phosphonium hexafluorophosphate (BOP reagent) and the resulting mixture was allowed to stir at room temperature overnight and was then concentrated to dryness. The residue was dissolved into ethyl acetate and washed with water, 0.5N HCl, saturated NaHCO3 and brine and then dried over MgSO4 and concentrated. Flash chromatography (elution with a gradient of 2-10% ether in methylene chloride) provided 2.0 g of the amide 139. 1H NMR consistent with structure.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05620971
出典データセットuspto-grants-1997_04
ORD IDord-335b9dd89de54030898409aded9b82d1
出典メモuspto-grants-1997_04