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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 970310Erstellt: 23. Oktober 2026

Piperazine → Cgp-74588

https://huagongshe.com/de/reaction/970310

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPiperazineHCID 4837—
Edukt4-(Chloromethyl)-N-(4-methyl-3-((4-(3-pyridinyl)-2-pyrimidinyl)amino)phenyl)benzamideHCID 10181075—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
ProduktCgp-74588HCID 9869737—

Reaktionsschritte

25.8 g (300 mmol) of piperazine are suspended in a mixture of 25 ml of ethanol and 25 ml of water. After almost a clear solution has formed, 12.9 g (30 mmol) of 4-chloromethyl-N-[4-methyl-3-(4-pyridin-3-yl-pyrimidin-2-ylamino)-phenyl]-benzamide are added step by step. The yellow solution is boiled under reflux for 14 hours, cooled to room temperature and filtered over Celite. 100 ml of water is added to the solution, the ethanol is evaporated under vacuum and 30 ml of 1N NaOH is added, leading to crystallization of the product. Drying at 50 mbar and 60° C. yields N-[4-methyl-3-(4-pyridin-3-yl-pyrimidin-2-ylamino)-phenyl]-4-piperazin-1-ylmethyl-benzamide; Rf=0.15 (methylene chloride:ethyl acetate:methanol:conc. aqueous ammonium hydroxide solution=60:10:30:2); tR (HPLC)2) 14.6 min.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07312216B2
Quelldatensatzuspto-grants-2007_12
ORD IDord-bda9621ad94543d4bb433a1bdaebf06b
Quellennotizuspto-grants-2007_12