Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1-(4-FLUORO-PHENYL)-1H-PYRAZOL-3-AMINE | HCID 13626944 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Reactant | Ethyl 6-methyl-3-(5-pyrimidinylamino)-2-pyridinecarboxylate | HCID 58368053 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 53330914 | HCID 53330914 | — |
Reaction Steps
1-(4-Fluoro-phenyl)-1H-pyrazol-3-ylamine (55 mg, 0.31 mmol) was dissolved under inert gas atmosphere in dioxane (2 ml) and trimethylaluminium (0.154 ml, 2M toluene solution) was added. After stirring for 30 min at ambient temperature, 6-methyl-3-(pyrimidin-5-ylamino)-pyridine-2-carboxylic acid ethyl ester (A-1; 20 mg, 0.08 mmol) was added and the reaction mixture was heated at reflux for 18 hours. Upon cooling to room temperature water (0.5 ml) was added and intensive stirring was continued for 5 min. Sufficient sodium sulfate for water absorption and dichloromethane were added while stirring is continued. The resulting solution was then filtered through decalite and washed with dichloromethane. The solvent was evaporated and the final product was obtained after silica gel chromatography using a heptane/ethyl acetate gradient as off-white solid (5 mg, 16%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08470820B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-2adae1deadec4637bc1e209228e41307 |
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| Source note | uspto-grants-2013_06 |
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