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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 729628Generated: October 29, 2026

Methanesulfonic Acid → 1-{1-[1-(2,6-Difluoro-benzoyl)-piperidin-4-yloxy]-isoquinolin-4-yl}-3-[5-(2-fluoro-1-fluoromethyl-1-methyl-ethyl)-2-p-tolyl-2H-pyrazol-3-yl]-urea mesylate

https://huagongshe.com/reaction/729628

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
Reactant1-{1-[1-(2,6-Difluoro-benzoyl)-piperidin-4-yloxy]-isoquinolin-4-yl}-3-[5-(2-fluoro-1-fluoromethyl-1-methyl-ethyl)-2-p-tolyl-2H-pyrazol-3-yl]-ureaHCID 69055075—
SolventDichloromethaneHCID 6344—
Product1-{1-[1-(2,6-Difluoro-benzoyl)-piperidin-4-yloxy]-isoquinolin-4-yl}-3-[5-(2-fluoro-1-fluoromethyl-1-methyl-ethyl)-2-p-tolyl-2H-pyrazol-3-yl]-urea mesylateHCID 86624447—

Reaction Steps

Dissolve 0.13 g (0.19 mmol) of 1-{1-[1-(2,6-Difluoro-benzoyl)-piperidin-4-yloxy]-isoquinolin-4-yl}-3-[5-(2-fluoro-1-fluoromethyl-1-methyl-ethyl)-2-p-tolyl-2H-pyrazol-3-yl]-urea in dichloromethane (2 mL) and add 0.19 mL of a solution of methanesulfonic acid 1 N in dichloromethane. Evaporation of solvent under reduced pressure gives 0.09 g of the title compound as a white solid. ES+ (m/z) 675 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582638B2
Source datasetuspto-grants-2009_09
ORD IDord-c57b94ca4e674d89b410d7cf57e23fe4
Source noteuspto-grants-2009_09