HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → 2-[{4-(2-Pyridinyl)Benzyl}Oxy]-6-(1-Piperazinyl)Pyrazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (4-(Pyridin-2-yl)phenyl)methanol | HCID 1515239 | — |
| Reactant | 4-Pyridin-2-ylbenzaldehyde | HCID 1515240 | — |
| Reactant | 2-Chloro-6-[{4-(2-pyridinyl)benzyl}oxy]pyrazine | HCID 18186935 | — |
| Product | 2-[{4-(2-Pyridinyl)Benzyl}Oxy]-6-(1-Piperazinyl)Pyrazine | HCID 18186937 | — |
Reaction Steps
The title compound was prepared according to the procedure of example 50, step 2, starting from 2-chloro-6-[{4-(2-pyridinyl)benzyl}oxy]pyrazine (2.73 g, 9.16 mmol; obtained according to the procedure of example 50, step 1, starting from 4-(2-pyridinyl)benzyl alcohol*), piperazine (2.41 g, 27.9 mmol) and K2CO3 (1.33 g, 9.62 mmol) with the exception that the final filtration through alumina was omitted. The yield of the of the title compound was 2.06 g (65%) which was obtained as a beige colored oil that solidified when refrigerated. Purity 100% (HPLC). MS m/z 347 (M)+. HRMS m/z calcd for C20H21N5O (M)+ 347.1746, found 347.1749. *Obtained by reduction (NaBH4) of 4-(2-pyridyl)benzaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07247633B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-b295db703f8c42608a69355c3bbef798 |
| Source note | uspto-grants-2007_07 |