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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 20081Erstellt: 24. Oktober 2026

4,5-Diaminopyrimidine → 4-Amino-5-[(1-t-butoxycarbonylpiperidin-4-yl)amino)pyrimidine

https://huagongshe.com/reaction/20081

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4,5-DiaminopyrimidineHCID 83703—
Edukttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
EduktSodium triacetoxyborohydrideHCID 5049666—
Lösungsmittel1,1-DichloroethaneHCID 6365—
Produkt4-Amino-5-[(1-t-butoxycarbonylpiperidin-4-yl)amino)pyrimidineHCID 22293202—

Reaktionsschritte

A mixture of 4,5-diaminopyrimidine (1.0 g, 9.1 mmol), N-(t-butoxycarbonyl)-4-piperidone (3.0 g, 15 mmol) and sodium triacetoxyborohydride (1.2 g, 5.6 mmol) in dichloroethane (60 mL) was stirred at room temperature for 3 d. The reaction was partitioned between chloroform (200 mL) and 3N sodium hydroxide (30 mL). After drying over magnesium sulfate, the organic phase was concentrated to give the title compound as a tan gum. MS 294 (M+1)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07745427B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-0dd8899708d64386a753695d6bbd50b9
Quellennotizuspto-grants-2010_06