Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 4-Aminobenzonitrile | HCID 13396 | — |
| Reactant | HCID 90051808 | HCID 90051808 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 90052203 | HCID 90052203 | 91.9% |
Reaction Steps
To a solution of 2-(5-(2-chloro-4-methyl-6-(propylamino)pyrimidin-5-yl)-4-pentyn-1-yl)isoindoline-1,3-dione (T3, 65 mg) in 1,4-dioxane (3 mL), 4-aminobenzonitrile (29 mg), cesium carbonate (133 mg), tris(dibenzylideneacetone)dipalladium(0) (30 mg) and 4,5′-bis(diphenylphosphino)-9,9′-dimethylxanthene (38 mg) were added at room temperature, the reaction vessel was sealed, and then by using a microwave reaction system, the mixture was stirred at 160° C. for 20 minutes. The reaction mixture was cooled to room temperature, and then ethyl acetate was added to the reaction mixture. The insoluble matter was removed by filtration through Cerite, and then the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (eluent, 90 to 50% hexane in ethyl acetate) to obtain 4-((5-(5-(1,3-dioxoisoindolin-2-yl)-1-pentyn-1-yl)-4-methyl-6-(propylamino)pyrimidin-2-yl)amino)benzonitrile (T4, 72 mg) as pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09145415B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-55874ce1a4f04baea418989291d1fad6 |
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| Source note | uspto-grants-2015_09 |
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