Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-(Tetramethyl-1,3,2-dioxaborolan-2-yl)aniline | HCID 2734620 | — |
| Reactant | HCID 59380097 | HCID 59380097 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | HCID 59380005 | HCID 59380005 | 82.9% |
Reaction Steps
Sodium carbonate (2M in water, 6.69 mL, 13.38 mmol) was added to 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline (0.815 g, 3.72 mmol) and 2-chloro-4-[2-(4-chlorophenyl)sulfonylpropan-2-yl]-6-[(3S)-3-methylmorpholin-4-yl]pyrimidine (1.60 g, 3.72 mmol) in a mixture of DME (10 mL), ethanol (10.00 mL), DMF (10.00 mL) and water (20 mL) at RT under nitrogen. The mixture was degassed and purged with nitrogen three times. Bis(triphenylphosphine)palladium(II) chloride (0.130 g, 0.19 mmol) was added and the mixture was degassed and purged with nitrogen a further three times. The resulting suspension was stirred under nitrogen at 80° C. for 90 minutes. The reaction mixture was concentrated and diluted with ethyl acetate (150 mL) and washed with water (2×150 mL) and saturated brine (100 mL). The organic layer was dried (MgSO4), filtered and evaporated. The crude product was purified by flash silica chromatography, elution gradient 30 to 45% ethyl acetate in isohexane, to give the desired material as a white solid (1.502 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07750003B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-dbd1dd2c9c7640c1add8a515b00ab959 |
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| Source note | uspto-grants-2010_07 |
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