Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 43114742 | HCID 43114742 | — |
| Reactant | HCID 178426381 | HCID 178426381 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | Imatinib amine | HCID 9965429 | — |
Reaction Steps
Under inert atmosphere, 16 g sodium salt of β-oxo-3-pyridinepropanal, with HPLC purity of 99% (A %) and 25% salt content (residue by calcination), and 11.7 g (2-methyl-5-aminophenyl)guanidine in 115 mL n-butanol is suspended. 9 mL acetic acid is added, and the mixture is stirred at room temperature for an hour. 6 g potassium hydroxide is added portionwise, and the mixture is refluxed for 18 hours, removing the water with a Dean Stark apparatus. Once completed the conversion, the suspension is cooled and the organic layer is washed with water. The organic layer is concentrated to a small volume, and toluene is added. The precipitate is filtrated, yielding, upon drying, 15.5 g of product with HPLC purity of 99.2% (A %), identified through LC-MS and 1H-NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08168787B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-33dced4969a047a690454452938d75dd |
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| Source note | uspto-grants-2012_05 |
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