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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 490099Generated: October 30, 2026

Ethyl Acetate → 5-(4-Boc-piperazin-1-yl)-3-chloro[1,2,4]triazine

https://huagongshe.com/reaction/490099

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant3,5-Dichloro-1,2,4-triazineHCID 12264933—
Solvent1,4-DioxaneHCID 31275—
Product5-(4-Boc-piperazin-1-yl)-3-chloro[1,2,4]triazineHCID 5767418631.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07528132B2
Source datasetuspto-grants-2009_05
ORD IDord-b9250beff4904051a0e31e6027b56d63
Source noteuspto-grants-2009_05