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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1791999Erstellt: 27. Oktober 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → 4-(7-Allyl-1,3-dimethyl-2,6-dioxo-2,3,6,7-tetrahydro-1H-purin-8-yl)piperazine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1791999

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Edukttert-Butyl piperazine-1-carboxylateHCID 143452—
Edukt7-Allyl-8-chloro-1,3-dimethyl-3,7-dihydropurine-2,6-dioneHCID 738682—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
Produkt4-(7-Allyl-1,3-dimethyl-2,6-dioxo-2,3,6,7-tetrahydro-1H-purin-8-yl)piperazine-1-carboxylic acid tert-butyl esterHCID 2353695394,4%

Reaktionsbedingungen

Temperatur140 °C

Reaktionsschritte

A mixture of 7-allyl-8-chloro-1,3-dimethyl-3,7-dihydropurine-2,6-dione (1.0 g), piperazine-1-carboxylic acid tert-butyl ester (1.1 g), 1,8-diazabicyclo[5,4,0]undec-7-ene (DBU) (0.59 ml), and 1-methylpyrrolidin-2-one (2 ml) were stirred under nitrogen atmosphere in an oil bath at 140° C. for 2 hours. The reaction mixture was extracted with ethyl acetate and water. The organic layer was washed with water followed by saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography with 10–20% (20% 2-propanol/ethyl acetate)/hexane to give 1.5 g of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07074798B2
Quelldatensatzuspto-grants-2006_07
ORD IDord-c838971beba043dab0973b4dd0a71f71
Quellennotizuspto-grants-2006_07