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HRID 240058Erstellt: 25. Oktober 2026

Diisopropylethylamine → 8-Trifluoromethoxy-2-oxo-2H-chromene-3-carboxylic acid (4'-Methoxy-3'-methyl-biphenyl-3-yl)-amide

https://huagongshe.com/reaction/240058

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
EduktMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Edukt4'-Methoxy-3'-methyl-biphenyl-3-ylamineHCID 39243256—
Edukt8-Trifluoromethoxy-3-carboxy-coumarinHCID 86650358—
LösungsmittelDimethylformamideHCID 6228—
Produkt8-Trifluoromethoxy-2-oxo-2H-chromene-3-carboxylic acid (4'-Methoxy-3'-methyl-biphenyl-3-yl)-amideHCID 4419765467%

Reaktionsschritte

DIEA (0.014 mL, 0.077 mmol) was added to 8-trifluoromethoxy-3-carboxy-coumarin (0.019 g, 0.070 mmol) and HATU (0.029 g, 0.077 mmol) in 0.36 mL of DMF with constant stirring at room temperature until a clear solution resulted. Subsequently, 4′-Methoxy-3′-methyl-biphenyl-3-ylamine (0.015 g, 0.070 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 0.022 g of product in 65% yield: LCMS (ESI) m/z 470 (MH+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08642788B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-9464a3998fe3415b9c8bb2ad38dc27e9
Quellennotizuspto-grants-2014_02