Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 240016Erstellt: 26. Oktober 2026

4-Aminopyrimidine → 8-Methoxy-2-oxo-2H-chromene-3-carboxylic acid pyrimidin-4-ylamide

https://huagongshe.com/reaction/240016

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-AminopyrimidineHCID 68958—
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—
LösungsmittelDimethylformamideHCID 6228—
Produkt8-Methoxy-2-oxo-2H-chromene-3-carboxylic acid pyrimidin-4-ylamideHCID 8665036211,2%

Reaktionsschritte

DIEA (0.044 mL, 0.25 mmol) was added to 8-methoxy-3-carboxy-coumarin (0.030 g, 0.14 mmol) and HATU (0.095 g, 0.25 mmol) in 1 mL of dimethylformamide (DMF) with constant stirring at room temperature until a clear solution resulted. Subsequently, pyrimidin-4-ylamine (0.009 g, 0.09 mmol) was added and allowed to react overnight, when a solid precipitated out of solution. The precipitate was filtered and dried under suction and then in vacuo to give 0.003 g of 1541E in an 11% yield: LCMS (ESI) m/z 298 (MH+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08642788B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-2d51c4b1ed764bf48d22b69a4e99b14e
Quellennotizuspto-grants-2014_02