HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → HCID 18186926, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | o-Phenethylbenzyl alcohol | HCID 70040 | — |
| Reactant | HCID 18186871 | HCID 18186871 | — |
| Product | HCID 18186926 | HCID 18186926 | — |
Reaction Steps
The title compound was prepared according to the procedure of example 50, step 2, starting from 2-chloro-6-{[2-(2-phenylethyl)benzyl]oxy}pyrazine (1.72 g, 5.30 mmol; obtained according to the procedure of example 50, step 1, starting from 2-phenethylbenzyl alcohol), piperazine (1.37 g, 16.0 mmol) and K2CO3 (0.73 g, 5.3 mmol). The yield of the title compound was 1.38 g (69%) which was obtained as an oil. Purity 100% (HPLC). MS m/z 375 (M+H)+. HRMS m/z calcd for C23H26N4O (M)+ 374.2107, found 374.2113.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07247633B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-0e22a622d0b24a12a1cfdc882718d91e |
| Source note | uspto-grants-2007_07 |