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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 240043Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/240043

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt3-(Pyridin-3-yl)anilineHCID 459521—
Edukt8-Hydroxy-3-carboxy-coumarinHCID 7245716—
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-Hydroxy-2-oxo-2H-chromene-3-carboxylic acid (3-pyridin-3-yl-phenyl)-amideHCID 8665036632,5%

Reaktionsschritte

DIEA (0.028 mL, 0.160 mmol) was added to 8-hydroxy-3-carboxy-coumarin (0.030 g, 0.146 mmol) and HATU (0.061 g, 0.160 mmol) in 0.5 mL of DMF with constant stirring at room temperature until a clear solution resulted. Subsequently, 3-pyridin-3-ylaniline (0.025 g, 0.146 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 0.017 g of product in 32% yield: LCMS (ESI) m/z 359 (MH+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08642788B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-1cfbbbeed21e41c8a76608fed56d1869
Quellennotizuspto-grants-2014_02