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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1798738Generated: October 25, 2026

Hydrochloric Acid → Dimethylol glycol

https://huagongshe.com/reaction/1798738

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
ReactantNilotinibHCID 644241—
ReactantNilotinib Hydrochloride AnhydrousHCID 16006490—
ProductDimethylol glycolHCID 62511—
ProductNilotinibHCID 644241—

Reaction Conditions

Temperature42 °C

Reaction Steps

4.0 g 4-methyl-N-[3-(4-methyl-imidazol-1-yl)-5-trifluoromethyl-phenyl]-3-(4-pyridin-3-yl-pyrimidin-2-ylamino)-benzamide free base is dissolved in 60 mL methanol at 50° C. 1.05 equivalent (688.7 μL) of hydrochloric acid is added as a solution in 2 mL of methanol. The solution is let stand for 60 minutes at 50° C. The solution is cooled down to 42° C. and kept at this temperature for 15 minutes. A suspension of 4 mg of 4-methyl-N-[3-(4-methyl-imidazol-1-yl)-5-trifluoromethyl-phenyl]-3-(4-pyridin-3-yl-pyrimidin-2-ylamino)-benzamide hydrochloride in methanol (40 mg)/water (0.4 mg) homogenized for 10 seconds in an ultrasonic bath is added. The suspension is let stand for 2.5 hours at 42° C., then cooled down in 7 hours at 20° C. The suspension remains at 20° C. for 56 hours. The suspension is not filtrated before analysis. The dimethanol solvate form SB of the hydrochloride salt of 4-methyl-N-[3-(4-methyl-imidazol-1-yl)-5-trifluoromethyl-phenyl]-3-(4-pyridin-3-yl-pyrimidin-2-ylamino)-benzamide is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08343984B2
Source datasetuspto-grants-2013_01
ORD IDord-5c4b4a013e8443fe8a6601ffb3e31a26
Source noteuspto-grants-2013_01