Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 58553813 | HCID 58553813 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 58553808 | HCID 58553808 | — |
Reaction Steps
Process 1: To the acetonitrile (1 mL) solution of 4′-{[4-butyl-1-(5-hydroxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}biphenyl-2-carbonitrile (68 mg, 0.15 mmol), potassium carbonate (41 mg, 0.30 mmol) and iodoethane (70 mg, 0.448 mmol) were added and stirred at 60° C. for 5 hrs. After that, the reaction mixture was filtered and washed with ethyl acetate. The filtrate was distilled off to obtain 4′-{[4-butyl-1-(5-ethoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}biphenyl-2-carbonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08664226B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-d9bdc417669d4570b9e304ed66acef54 |
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| Source note | uspto-grants-2014_03 |
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