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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 883Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/883

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIndole-3-Butyric AcidHCID 8617—
EduktN,N-dimethylhydroxylamine hydrochlorideHCID 27969—
EduktDiisopropylethylamineHCID 81531—
EduktBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
LösungsmittelAcetonitrileHCID 6342—
ProduktN-Methyl-N-Methoxy-4-(3-indolyl)butyramideHCID 1110763194,3%

Reaktionsschritte

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-yloxy-tris(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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05723459
Quelldatensatzuspto-grants-1998_03
ORD IDord-5ab94114d8b645e082906ef9a74075cf
Quellennotizuspto-grants-1998_03