HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → HCID 18186810, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Phenoxybenzyl alcohol | HCID 26295 | — |
| Reactant | HCID 18186827 | HCID 18186827 | — |
| Product | HCID 18186810 | HCID 18186810 | — |
Reaction Steps
The title compound was prepared according to the procedure of example 50, step 2, starting from 2-chloro-6-[(3-phenoxybenzyl)oxy]pyrazine (1.99 g, 6.36 mmol; obtained according to the procedure of example 50, step 1, starting from 3-phenoxybenzyl alcohol), piperazine (1.94 g, 22.5 mmol) and K2CO3 (0.88 g, 6.4 mmol). The yield of the title compound was 1.58 g (69%) which was obtained as an oil. Purity 100% (HPLC). MS m/z 363 (M+H)+. HRMS m/z calcd for C21H22N4O2 (M)+ 362.1743, found 362.1739.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07247633B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-4f3e963ed3474281b9c076612e7d64af |
| Source note | uspto-grants-2007_07 |