Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | L-Malic Acid | HCID 222656 | — |
| Reactant | HCID 131730213 | HCID 131730213 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 131730219 | HCID 131730219 | 76.9% |
Reaction Steps
N-(2-Fluoro-4-{[2-({[4-(4-methylpiperazin-1-yl)piperidin-1-yl]carbonyl}amino)pyridin-4-yl]oxy}phenyl)-N′-(4-fluorophenyl)cyclopropane-1,1-dicarboxyamide (31.4 mg) was suspended in ethanol (0.317 ml). (2S)-Malic acid (5.7 mg) was added to the suspension at room temperature, and the mixture was stirred at 50° C. to form a solution. The reaction mixture was stirred at room temperature for 18 hours. The precipitate was collected by filtration and washed with ethanol (0.158 ml, 2 times). It was then dried under aeration at room temperature for 30 minutes, and dried with warm air at 60° C. for 1 day to give the title compound (26.0 mg, 68%) as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08377938B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-dfd5fed5d8f14f8e88a172257144ac34 |
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| Source note | uspto-grants-2013_02 |
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