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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010806Generated: October 28, 2026

Imatinib → Imatinib Mesylate

https://huagongshe.com/reaction/1010806

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImatinibHCID 5291—
ReactantMethanesulfonic AcidHCID 6395—
SolventEthanolHCID 702—
ProductImatinib MesylateHCID 123596—

Reaction Steps

Imatinib base (3 g) was suspended in ethanol (60 ml, 96%) at −10° C. Methanesulfonic acid (0.375 ml) was added with stirring and the suspension was stirred for additional 20 min at −5° C. obtaining thus the solution of imatinib mesylate. Than the solution was allowed to crystallize without stirring at −5° C. for 3 hours. t-Butyl methyl ether (50 ml) was added, the white solid was filtered, washed with petrolether (50 ml) and dried in a stream of nitrogen for 1 h to obtain imatinib mesylate Form IV (3.18 g, yield: 89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977348B2
Source datasetuspto-grants-2011_07
ORD IDord-fc830f8574ce402a86692b50a5a74551
Source noteuspto-grants-2011_07