Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Fumaric Acid | HCID 444972 | — |
| Reactant | HCID 51036303 | HCID 51036303 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 131731755 | HCID 131731755 | 76.1% |
Reaction Steps
Next, 3-chloro-4-{4-[5-(3-{[glycyl(methyl)amino]methyl}phenyl)pyrimidin-2-yl]piperazin-1-yl}benzoic acid (2 g) was suspended in THF (40 ml)-H2O (40 ml), and fumaric acid (938 mg) was added thereto, followed by stirring at 90° C. for 1 hour. The reaction mixture was cooled to room temperature and the solvent was evaporated under reduced pressure. To the residue was added THF (20 ml)-H2O (20 ml), followed by stirring at 90° C. for 1 hour as it was suspended. The mixture was cooled to room temperature, followed by stirring overnight. After the mixture was filtered, washed with THF—H2O (1:1), and then dried at 50° C. for 5 hours under reduced pressure to obtain 3-chloro-4-{4-[5-(3-{[glycyl(methyl)amino]methyl}phenyl)pyrimidin-2-yl]piperazin-1-yl}benzoic acid hemifumarate (1.7 g) as a colorless crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08802679B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-bc85fe7fb4c84c76ad434be55cd99939 |
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| Source note | uspto-grants-2014_08 |
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