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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 59044Generated: October 25, 2026

Methanol → Imatinib Mesylate

https://huagongshe.com/reaction/59044

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantImatinibHCID 5291—
ReactantDichloromethaneHCID 6344—
ReactantMethanesulfonic AcidHCID 6395—
SolventWaterHCID 962—
ProductImatinib MesylateHCID 123596—

Reaction Conditions

Temperature50 °C

Reaction Steps

Imatinib free base (90 g), methanol (450 mL) and dichloromethane (270 mL) were stirred at 25° C. in round bottom flask in presence of nitrogen. Methanesulfonic acid (18 g) was slowly added to the reaction mixture at 25° C. Water (27 mL) was added and the reaction mixture was stirred for 2 hours. The reaction mixture was heated at 50° C. and concentrated to remove the solvent mixture. The residue was degassed at 60° C. and cooled to 25° C. Methyl tert-butyl ether (630 mL) was added to the reaction mixture and stirred for 45 minutes. The product was filtered and washed with methyl tert-butyl ether. The product was dried at 60° C. under high vacuum for 10 hours to obtain amorphous imatinib mesylate. Water content 0.90%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09439903B2
Source datasetuspto-grants-2016_09
ORD IDord-af1762d853804d258e309783c217d2cb
Source noteuspto-grants-2016_09