Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 736299Erstellt: 25. Oktober 2026

Methanesulfonic Acid → 4-(4-methylpiperazin-N-ylaminomethyl)-N-[4-methyl-3-(4-(pyridin-3-yl)pyrimidin-2-yl)aminophenyl]benzamide methanesulfonate

https://huagongshe.com/reaction/736299

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanesulfonic AcidHCID 6395—
Edukt4-(4-methylpiperazin-1-ylaminomethyl)-N-[4-methyl-3-(4-(pyridin-3-yl)pyrimidin-2-yl)aminophenyl]benzamideHCID 9892492—
LösungsmittelEthanolHCID 702—
Produkt4-(4-methylpiperazin-N-ylaminomethyl)-N-[4-methyl-3-(4-(pyridin-3-yl)pyrimidin-2-yl)aminophenyl]benzamide methanesulfonateHCID 8659534070,7%

Reaktionsschritte

4-(4-Methylpiperazin-1-ylaminomethyl)-N-[4-methyl-3-(4-(pyridin-3-yl)pyrimidin-2-yl)aminophenyl]benzamide (95 mg, 0.187 mmol) was dissolved in ethanol (8 ml), methanesulfonic acid (24 μl, 0.347 mmol) was added thereto, and the mixture was reacted at room temperature for 16 hours. The resulting solid was filtered and washed with acetone to give 4-(4-methylpiperazin-N-ylaminomethyl)-N-[4-methyl-3-(4-(pyridin-3-yl)pyrimidin-2-yl)aminophenyl]benzamide methanesulfonate (80 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07595323B2
Quelldatensatzuspto-grants-2009_09
ORD IDord-9427bd5b76ad4c588b5d29eb1c252ac1
Quellennotizuspto-grants-2009_09