HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1962099Generated: October 30, 2026
Nilotinib Hydrochloride Anhydrous → Nilotinib
https://huagongshe.com/reaction/1962099
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nilotinib Hydrochloride Anhydrous | HCID 16006490 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | Nilotinib | HCID 644241 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08415363B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-b04dec902abc4538bc69669b8507adce |
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| Source note | uspto-grants-2013_04 |
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