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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1926594Generated: November 3, 2026

Methanesulfonic Acid → 4-[(4-Methylpiperazin-1-yl)methyl]-n-{6-methyl-5-[(4-(pyrid-3-yl)pyrimid-2-yl)amino]pyrid-3-yl} benzamide methanesulfonic acid salt

https://huagongshe.com/reaction/1926594

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
Reactant4-[(4-methylpiperazin-1-yl)methyl]-N-{6-methyl-5-[(4-(pyrid-3-yl)pyrimid-2-yl)amino]pyrid-3-yl}benzamideHCID 69227800—
SolventMethanolHCID 887—
Product4-[(4-Methylpiperazin-1-yl)methyl]-n-{6-methyl-5-[(4-(pyrid-3-yl)pyrimid-2-yl)amino]pyrid-3-yl} benzamide methanesulfonic acid saltHCID 8774408383.7%

Reaction Steps

To a flask was added 4-[(4-methylpiperazin-1-yl)methyl]-N-{6-methyl-5-[(4-(3-pyridyl)-2-pyrimidyl)amino]-3-pyridyl}benzamide (2.0 g), methanesulfonic acid (0.40 g) and methanol (100 mL). After the solution was clear, the reaction mixture was concentrated under reduced pressure to about 20 mL and acetone was added to get a crystal. Filtrated and the solid was dried to give 4-[(4-methylpiperazin-1-yl)methyl]-N-{6-methyl-5-[(4-(pyrid-3-yl)pyrimid-2-yl)amino]pyrid-3-yl} benzamide methanesulfonic acid salt (2.0 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183242B2
Source datasetuspto-grants-2012_05
ORD IDord-ced7181a8b6a43d3a80d7bd66728e2db
Source noteuspto-grants-2012_05