Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | HCID 86759067 | HCID 86759067 | — |
| Product | HCID 68574778 | HCID 68574778 | — |
Reaction Steps
The title compound was prepared according to the procedure of example 20, starting from 1-(6-chloro-2-pyrazinyl)-trans-2,5-dimethylpiperazine (1.23 g, 5.40 mmol; obtained in step 1 above), benzyl alcohol (8.36 g, 77.3 mmol), and K-t-BuO (1.99 g, 17.7 mmol). The reaction mixture was heated at 95° C. for 5.5 h. The yield of the title compound was 0.47 g (29%) which was obtained as an oil. Purity 99% (HPLC). MS m/z 298 (M)+. HRMS m/z calcd for C17H22N4O (M)+ 298.1794, found 298.1798.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07247633B2 |
|---|
| Source dataset | uspto-grants-2007_07 |
|---|
| ORD ID | ord-551989a8b3184690aae338f33255a665 |
|---|
| Source note | uspto-grants-2007_07 |
|---|