Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 451412Erstellt: 25. Oktober 2026

Diisopropylethylamine → tert-butyl N-[1-(6-methylpyrimidin-4-yl)piperidin-4-yl]carbamate

https://huagongshe.com/reaction/451412

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt4-Chloro-6-methylpyrimidineHCID 581796—
Edukt4-Amino-1-Boc-piperidineHCID 1268291—
LösungsmittelWaterHCID 962—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkttert-butyl N-[1-(6-methylpyrimidin-4-yl)piperidin-4-yl]carbamateHCID 67343276—

Reaktionsbedingungen

Temperatur150 °C

Reaktionsschritte

A suspension of Boc-4-aminopiperidine (613 mg, 3 mmol), 4-chloro-6-methylpyrimidine (433 mg, 3.3 mmol) and N,N-diisopropylethyl amine (771 L, 4.5 mmol) in dioxane (12 mL) was heated to 150° C. in the microwave for 30 minutes. The reaction was diluted with water and extracted twice with ethyl acetate. The combined organic layers were washed with water, dried over sodium sulfate, filtered and concentrated under reduced pressure. The crude product was purified by column chromatography on silica gel using a gradient from AcOEt to AcOEt/EtOH 9:1 as eluent. The title compound was obtained as a light yellow solid (693 mg, 79%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08486967B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-6de883d95cf14582bc0237df04c0840d
Quellennotizuspto-grants-2013_07