Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-(Tetramethyl-1,3,2-dioxaborolan-2-yl)aniline | HCID 2734620 | — |
| Reactant | HCID 59380175 | HCID 59380175 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | HCID 59380082 | HCID 59380082 | 69.9% |
Reaction Steps
Bis(triphenylphosphine)palladium(II) chloride (200 mg, 0.28 mmol) was added to 2-chloro-4-[(3S)-3-methylmorpholin-4-yl]-6-[2-[2-(trifluoromethyl)phenyl]sulfonylpropan-2-yl]pyrimidine (1.91 g, 4.12 mmol), 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline (1.353 g, 6.18 mmol) and sodium carbonate (10 mL, 20.00 mmol) in a mixture of ethanol (5 mL), DMF (10 mL), water (7 mL) and DME (25 mL) at RT. The resulting mixture was degassed then stirred at 95° C. for 18 hours. The reaction mixture was allowed to cool and diluted with ethyl acetate (200 mL), and washed with water (2×200 mL), and brine (100 mL). The organic layer was dried (Na2SO4), filtered and evaporated to afford crude product. The crude product was purified by flash silica chromatography, elution gradient 10 to 60% ethyl acetate in isohexane, and the resultant material triturated with a mixture of diethyl ether and isohexane to give the desired material as a white solid (1.50 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-cfac0267c9024b87957700268d6d674e |
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| Source note | uspto-grants-2010_07 |
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