Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorous acid | HCID 107909 | — |
| Reactant | Nilotinib | HCID 644241 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 16006179 | HCID 16006179 | — |
Reaction Steps
To a 1 L round-bottom flask equipped with a mechanical stirrer, a thermometer, and a condenser, 4-methyl-N-[3-(4-methyl-imidazol-1-yl)-5-trifluoromethyl-phenyl]-3-(4-pyridin-3-yl-pyrimidin-2-ylamino)-benzamide free base and 500 mL of methanol were charged. The slurry was stirred and heated to 64° C. and held at that temperature for ˜30 minutes. To the resulting clear solution, 7.5 mL of 1 M phosphorous acid solution (in methanol) was added. The mixture was stirred at 64° C. for one hour, cooled down to room temperature by natural cooling (cooling rate ˜0.5° C./min) and held at room temperature for 3-4 hours. The solid was collected by filtration and was dried at 50-55° C./10-20 torr for 8-16 hours to obtain 4-methyl-N-[3-(4-methyl-imidazol-1-yl)-5-trifluoromethyl-phenyl]-3-(4-pyridin-3-yl-pyrimidin-2-ylamino)-benzamide monophosphate salt (3.25 g) as a white solid. Melting point=˜208° C. (dec.); x-ray diffraction pattern showing maxima at 2θ=6.1°, 7.5°, 9.1°, 15.8°, 17.5°, 18.3°, 21.8°, 23.1°, 24.9°, 26.6°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08580806B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-99e79e2cc935478b892fafde17cffb8e |
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| Source note | uspto-grants-2013_11 |
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