HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → 5-(4-Boc-piperazin-1-yl)-3-chloro[1,2,4]triazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | 3,5-Dichloro-1,2,4-triazine | HCID 12264933 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 5-(4-Boc-piperazin-1-yl)-3-chloro[1,2,4]triazine | HCID 57674186 | 31.1% |
Reaction Steps
To a solution of 3,5-dichloro[1,2,4]triazine (0.34 g, 2.28 mmol.) in anhydrous dioxane (4 mL) was add diisopropylethylamine (0.44 g, 3.41 mmol.) and N—Boc-piperazine (0.424 g, 2.28 mmol.). The reaction mixture was stirred at room temperature for 40 minutes. Ethyl acetate (200 mL) was added. The organic solution was washed with saturated ammonium chloride solution, water and brine. The organic layer was dried over sodium sulfate. The organic solvent was evaporation under reduced pressure. The crude product was purified by RP-HPLC to yield the desired 5-(4-Boc-piperazin-1-yl)-3-chloro[1,2,4]triazine 151 (0.212 g, 0.71 mmol.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07528132B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-b9250beff4904051a0e31e6027b56d63 |
| Source note | uspto-grants-2009_05 |