HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428295Generated: November 1, 2026
N-methyl-2-pyrrolidone → HCID 86688194, compound
https://huagongshe.com/reaction/1428295
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | Maleic Acid | HCID 444266 | — |
| Reactant | Nilotinib | HCID 644241 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | HCID 86688194 | HCID 86688194 | — |
Reaction Steps
Nilotinib base (3.85 g, 7.27 mmol) was suspended in TFE (19 ml, 5V) and the mixture was heated to 40° C. with stirring. To the resulting cloudy yellow solution, maleic acid (0.84 g, 7.27 mmol) was added in one portion, followed by TFE (19 ml, 5V) at 45-50° C. Dissolution of the solid was achieved after about 5 min stirring at the same temperature. The resulting clear yellow solution was then stirred at 45° C. for about 3 h, and then at room temperature overnight (about 19 h). MTBE (10V) was added with stirring, leading to immediate precipitation. The resulting slurry was stirred for 1 h at room temperature and then the solid was separated from the mother liquors by filtration. The yellow solid was isolated and dried in a vacuum oven (35 mmHg) at 40° C. for 18.5 h to give Nilotinib maleate form IV (3.49 g, 74%) as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08937082B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-ad0bc6a8412e447a887cfbc96ca6470f |
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| Source note | uspto-grants-2015_01 |
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