Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 90051756 | HCID 90051756 | — |
| Reactant | tert-butyl ((1S,3R)-3-ethynylcyclohexyl)carbamate | HCID 90051794 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 117861302 | HCID 117861302 | 103.5% |
Reaction Steps
To a solution of N2-(3-fluorophenyl)-5-iodo-N4-propylpyrimidine-2,4-diamine (F2, 100 mg), bis(triphenylphosphine)palladium(II) dichloride (19 mg) and copper(I) iodide (10 mg) in N,N-dimethylformamide (2.7 mL), triethylamine (188 μL) and tert-butyl ((1S*,3R*)-3-ethynylcyclohexyl)carbamate (M3, 90 mg) were added at room temperature, and the mixture was stirred at the same temperature for 1 hour and 45 minutes. To the reaction mixture, water and ethyl acetate were added. The organic layer was separated, washed successively with saturated ammonium chloride and saturated aqueous sodium chloride, and then dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (eluent, 94 to 60% hexane in ethyl acetate) to obtain tert-butyl ((1S*,3R*)-3-((2-((3-fluorophenyl)amino)-4-(propylamino)pyrimidin-5-yl)ethynyl)cyclohexyl)carbamate (M4, 130 mg) as yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09145415B2 |
|---|
| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-2eaf16f5622e4b509b2fc9584c13e05e |
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| Source note | uspto-grants-2015_09 |
|---|