Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | HCID 86759066 | HCID 86759066 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 68574100 | HCID 68574100 | — |
Reaction Steps
To a solution of (2S)-1-(6-chloro-2-pyrazinyl)-2-methylpiperazine (prepared in step 2 above; 0.16 g, 0.72 mmol) and benzyl alcohol (0.12 g, 1.1 mmol) in DMF (4 mL) was Na-t-BuO (0.14 g, 1.4 mmol) added and the mixture was stirred at 150° C. overnight. The solvent was evaporated off under reduced pressure and the residue taken up between CHCl3/H2O. The organic phase was concentrated and the crude product was purified by preparative C18-HPLC using acetonitrile/H2O/HOAc with UV detection at 254 nm. Yield: 1 mg (0.4%). MS m/z 284 (M)+. HRMS m/z calcd for C16H20N4O (M)+ 284.1637, found 284.1640.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07247633B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-3fad84b7126d4234b7b96a283ddbe675 |
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| Source note | uspto-grants-2007_07 |
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