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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 729626Generated: October 30, 2026

Methanesulfonic Acid → 1-{1-[1-(1-Methyl-cyclopropanecarbonyl)-piperidin-4-yloxy]-isoquinolin-4-yl}-3-[5-(1-methyl-cyclopropyl)-2-p-tolyl-2H-pyrazol-3-yl]-urea mesylate

https://huagongshe.com/reaction/729626

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
Reactant1-{1-[1-(1-Methyl-cyclopropanecarbonyl)-piperidin-4-yloxy] isoquinolin-4-yl}-3-[5-(1-methyl-cyclopropyl)-2-p-tolyl-2H-pyrazol-3-yl]-ureaHCID 16061469—
SolventDichloromethaneHCID 6344—
Product1-{1-[1-(1-Methyl-cyclopropanecarbonyl)-piperidin-4-yloxy]-isoquinolin-4-yl}-3-[5-(1-methyl-cyclopropyl)-2-p-tolyl-2H-pyrazol-3-yl]-urea mesylateHCID 86624446—

Reaction Steps

Dissolve 0.3 g of 1-{1-[1-(1-Methyl-cyclopropanecarbonyl)-piperidin-4-yloxy] isoquinolin-4-yl}-3-[5-(1-methyl-cyclopropyl)-2-p-tolyl-2H-pyrazol-3-yl]-urea in dichloromethane 1 mL and add 321 μL of a solution of methanesulfonic acid 1 N in dichloromethane. Evaporation of solvent under reduced pressure gives 0.357 g of the title compound as a white solid (quantitative). ES+ (m/z) 579.3 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582638B2
Source datasetuspto-grants-2009_09
ORD IDord-e7bbacc1f2094e1f9dc3e1d996d03727
Source noteuspto-grants-2009_09