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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 490117Erstellt: 25. Oktober 2026

3-Piperidinecarboxamide → 1-(6-(2-Amino-6-methylpyrazolo[1,5-a]pyrimidin-3-yl)pyrimidin-4-yl)piperidine-3-carboxamide

https://huagongshe.com/reaction/490117

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-PiperidinecarboxamideHCID 92980—
Edukt6-Methyl-3-(6-(methylsulfinyl)pyrimidin-4-yl)pyrazolo[1,5-a]pyrimidin-2-amineHCID 57674595—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
Produkt1-(6-(2-Amino-6-methylpyrazolo[1,5-a]pyrimidin-3-yl)pyrimidin-4-yl)piperidine-3-carboxamideHCID 57674397—

Reaktionsbedingungen

Temperatur200 °C

Reaktionsschritte

6-methyl-3-(6-(methylsulfinyl)pyrimidin-4-yl)pyrazolo[1,5-a]pyrimidin-2-amine (60 mg, 0.21 mmol) was dissolved in NMP with nipecotamide (100 mg, 0.78 mmol)and heated to 200° C. in a microwave for 20 min. The reaction mixture was purified by RP HPLC (C18, CH3CN/H2O 0.1% TFA) and the pure fractions were poured into ethyl acetate/0.5 N NaOH. The organic phase was dried over sodium sulfate and concentrated to a yellow solid which was dissolved in 1N HCl in MeOH and concentrated to the HCl salt as a yellow solid, 20 mg, 0.052 mmol, 26%. LC/MS MH+353.4

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07528138B2
Quelldatensatzuspto-grants-2009_05
ORD IDord-1dfbe04131354aeebcbb416aa8e745be
Quellennotizuspto-grants-2009_05