Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1597878Erstellt: 26. Oktober 2026

Benzene → HCID 178466938, Verbindung

https://huagongshe.com/reaction/1597878

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzeneHCID 241—
EduktWaterHCID 962—
Edukt4-(Diethylamino)-2-ethoxybenzaldehydeHCID 958708—
Edukt5-amino-1-cyclopentyl-3-ethyl-1H-pyrazole-4-carboxamideHCID 22449352—
KatalysatorPalladiumHCID 23938—
Katalysatorp-Toluenesulfonic acid monohydrateHCID 521998—
LösungsmittelHexaneHCID 8058—
ProduktHCID 178466938HCID 17846693815,8%

Reaktionsschritte

A mixture of 2-ethoxy-4-(diethylamino)benzaldehyde (7.87 g, 35.56 mmol), 1-cyclopentyl-3-ethyl-5-amino-1H-pyrazole-4-carboxamide (3.95 g, 17.78 mmol), p-toluenesulfonic acid monohydrate (0.05 g), 10% palladium on carbon (0.11 g) and benzene (150 ml) was refluxed overnight with the azeotropic removal of water. The catalyst was removed by filtration, and the filtrate was concentrated in vacuo. The residue was combined with that from a similar experimental run, and dissolved in CH2Cl2, and loaded onto a silica gel column. Elution of the column with ether/hexane (60/40) afforded a green foam which was titurated with refluxing hexane, and cooled and the product, as pale yellow needles, was collected by filtration to afford 1.19 g (8%) of 1-cyclopentyl-3-ethyl-6-[2-ethoxy-4-(diethylamino)phenyl]pyrazolo[3,4-d]pyrimidin-4-one, m.p. 138°-139° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05736548
Quelldatensatzuspto-grants-1998_04
ORD IDord-99927a1a151947c7b17a9b1760151020
Quellennotizuspto-grants-1998_04