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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1752178Generated: October 30, 2026

Methanesulfonic Acid → HCID 16006386, compound

https://huagongshe.com/reaction/1752178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantNilotinibHCID 644241—
SolventEthyl AcetateHCID 8857—
ProductHCID 16006386HCID 16006386—

Reaction Conditions

Temperature76 °C

Reaction Steps

To a 75 mL reactor equipped with a temperature probe and a condenser, 307 mg of 4-methyl-N-[3-(4-methyl-imidazol-1-yl)-5-trifluoromethyl-phenyl]-3-(4-pyridin-3-yl-pyrimidin-2-ylamino)-benzamide free base and 30 mL of ethyl acetate were charged. The slurry was stirred and heated to 76° C. To the solution, 580 μL of 1 M methane sulfonic acid solution (in ethyl acetate) was added. The mixture was stirred at 76° C. for six hours, cooled to 25° C. at a rate of 0.5° C./minute and held at 25° C. overnight. The solid was collected by filtration and was dried at 50-55° C./10-20 torr for 8-16 hours to obtain 4-methyl-N-[3-(4-methyl-imidazol-1-yl)-5-trifluoromethyl-phenyl]-3-(4-pyridin-3-yl-pyrimidin-2-ylamino)-benzamide mesylate salt (˜250 mg) as a yellowish solid. X-ray diffraction pattern showing maxima at 2θ=7.7°, 10.1°, 20.3°, 26.2°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09163005B2
Source datasetuspto-grants-2015_10
ORD IDord-b1f65e1cb8e744aebba6d82662547c72
Source noteuspto-grants-2015_10