HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428313Generated: October 30, 2026
tert-Butyl methyl ether → HCID 86688194, compound
https://huagongshe.com/reaction/1428313
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl methyl ether | HCID 15413 | — |
| Reactant | Maleic Acid | HCID 444266 | — |
| Reactant | Nilotinib | HCID 644241 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86688194 | HCID 86688194 | — |
Reaction Steps
Nilotinib base form A (4.00 g, 7.55 mmol) was stirred with EtOH abs (40 mL, 10V) and the suspension was heated to 80° C. Stirring was continued at the same temperature for 30 min. To the stirred suspension was added a solution of maleic acid (0.96 g, 8.31 mol. 1.1 eq) in EtOH abs (10 mL, 2.5V) in one portion. The resulting mixture was stirred at 80° C. for 1 h and then cooled to room temperature and stirred for another 6 h. The solids were isolated by filtration to give Nilotinib maleate form V. The obtained Nilotinib maleate form V was dried in a vacuum oven (35 mmHg) at 60° C. for 16 hours. The dried product was analyzed by PXRD and was found to be Nilotinib maleate form V. Mono maleate was obtained as confirmed by assay determination.
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-a918427d839f429bb9fdf43bf615b9fe |
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| Source note | uspto-grants-2015_01 |
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