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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1798736Generated: November 1, 2026

Nilotinib Hydrochloride Anhydrous → Nilotinib

https://huagongshe.com/reaction/1798736

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNilotinib Hydrochloride AnhydrousHCID 16006490—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductNilotinibHCID 644241—

Reaction Conditions

Temperature65 °C

Reaction Steps

4-Methyl-N-[3-(4-methyl-imidazol-1-yl)-5-trifluoromethyl-phenyl]-3-(4-pyridin-3-yl-pyrimidin-2-ylamino)-benzamide hydrochloride (12 g) is suspended in 192 mL of methanol and 14.87 mL of water. The solution is heated to 64-66° C. in 10 minutes and kept for 5 minutes at 66° C. The solution is then cooled down to 42° C. in 15 minutes and then seeded. The suspension is kept for 2.5 hours at 42° C. and cooled down to 20° C. in 7 hours and cooled down within 6 hours at −10° C. The suspension is kept for 79 hours before filtration under vacuum. The solid is washed 2 times with a cold mixture of methanol/water 66 mL/5.26 mL (−10° C.) and dried under vacuum at 70° C. for 20 hours to obtain form C 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08343984B2
Source datasetuspto-grants-2013_01
ORD IDord-8902465b7011492fad183eedfe2b8f78
Source noteuspto-grants-2013_01