Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Butyl ether | HCID 8909 | — |
| Reactant | 2,3-Diphenylpyrazine | HCID 243907 | — |
| Reactant | HCID 178506676 | HCID 178506676 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2,3,5-Triphenylpyrazine | HCID 12430649 | 56% |
Reaction Steps
First, 5.5 mL of a dibutyl ether solution of phenyl lithium (manufactured by Wako Pure Chemical Industries, Ltd., 2.1 mol/L) and 50 mL of diethyl ether were mixed under a nitrogen atmosphere. Then, 2.43 g of 2,3-diphenylpyrazine was dropped into this solution while the solution was being cooled, with ice, and the mixture was stirred at room temperature for 24 hours. Water was added to the mixture, and the organic layer was extracted with diethyl ether. The extracted organic layer was washed with water and dried with magnesium sulfate. After the drying, an excess amount of activated manganese dioxide was added to the organic layer, and the mixture was filtered. After the solvent of the solution was distilled off, the obtained residue was recrystallized with ethanol to give a pyrazine derivative, Htppr (a yellow powder, 56% yield). The synthetic scheme of Step 1 is represented by (a-1) below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09012036B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-59c51348ec1e4892ad44b441a66370c5 |
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| Source note | uspto-grants-2015_04 |
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