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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 240044Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/240044

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt8-Methoxy-2-oxo-2H-chromene-3-carboxylic acidHCID 234562—
Edukt3-(Pyridin-3-yl)anilineHCID 459521—
EduktMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
LösungsmittelDimethylformamideHCID 6228—
Produkt8-Methoxy-2-oxo-2H-chromene-3-carboxylic acid (3-pyridin-3-yl-phenyl)-amideHCID 8665036784%

Reaktionsschritte

DIEA (43.5 μL, 0.25 mmol) was added to 8-methoxy-3-carboxy-coumarin (50.0 mg, 0.23 mmol) and HATU (95.0 mg, 0.25 mmol) in 1 mL of DMF with constant stirring at room temperature until a clear solution resulted. Subsequently, 3-pyridin-3-yl-phenylamine (38.7 mg, 0.23 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 71.6 mg of product in 84% yield: LCMS (ESI) m/z 373 (MH+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08642788B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-cd768fd000b74994a6aef355194d60bc
Quellennotizuspto-grants-2014_02