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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 68819Erstellt: 25. Oktober 2026

Diisopropylethylamine → N-Cyclopropyl-N-[1-(5-ethyl-pyrimidin-2-yl)-piperidin-4-yl]-4-oxazol-5-yl-benzamide

https://huagongshe.com/reaction/68819

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt2-Chloro-5-ethylpyrimidineHCID 3572763—
EduktN-cyclopropyl-4-oxazol-5-yl-N-piperidin-4-yl-benzamide hydrochlorideHCID 68289930—
LösungsmittelDimethylformamideHCID 6228—
Lösungsmittel1,4-DioxaneHCID 31275—
ProduktN-Cyclopropyl-N-[1-(5-ethyl-pyrimidin-2-yl)-piperidin-4-yl]-4-oxazol-5-yl-benzamideHCID 68290555—

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

A mixture of N-cyclopropyl-4-oxazol-5-yl-N-piperidin-4-yl-benzamide hydrogen chloride salt (52 mg), ethyldiisopropylamine (59 mg), and 2-chloro-5-ethylpyrimidine (21 mg) in N,N-dimethylformamide (1.0 mL) and 1,4-dioxane (1.5 mL) is stirred over night at 120° C. After cooling to room temperature, the solvents are evaporated and the residue is purified by HPLC (H2O/MeOH/TFA) to give the title compound. LC (method 9): tR=1.74 min; Mass spectrum (ESI+): m/z=418 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08822471B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-bf4170711eb04fa2b341ec10d300b61a
Quellennotizuspto-grants-2014_09