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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 240135Erstellt: 25. Oktober 2026

Diisopropylethylamine → 8-Methoxy-2-oxo-2H-chromene-3-carboxylic acid [3-(5-methoxy-pyridin-3-yl)-phenyl]-amide

https://huagongshe.com/reaction/240135

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt8-Methoxy-2-oxo-2H-chromene-3-carboxylic acidHCID 234562—
EduktMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Edukt3-(5-Methoxy-pyridin-3-yl)-phenylamineHCID 66865720—
LösungsmittelDimethylformamideHCID 6228—
Produkt8-Methoxy-2-oxo-2H-chromene-3-carboxylic acid [3-(5-methoxy-pyridin-3-yl)-phenyl]-amideHCID 8665042879%

Reaktionsschritte

DIEA (0.012 mL, 0.071 mmol) was added to 8-methoxy-3-carboxy-coumarin (0.014 g, 0.065 mmol) and HATU (0.027 g, 0.071 mmol) in 0.5 mL of DMF with constant stirring at room temperature until a clear solution resulted. Subsequently, 3-(5-methoxy-pyridin-3-yl)-phenylamine (0.013 g, 0.065 mmol) was added and allowed to react overnight when a solid precipitated out of solution. The resulting precipitate was filtered, dried under suction, and finally dried overnight in vacuo to give 0.020 g of product in 79% yield: LCMS (ESI) m/z 403 (MH+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08642788B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-3c3fc12b3e32460486b3e222cfa7f64c
Quellennotizuspto-grants-2014_02