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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 84763Generated: October 29, 2026

Water → 2-Bromo-1-(4-pyridin-2-yl-piperazin-1-yl)-ethanone

https://huagongshe.com/reaction/84763

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantBromoacetyl bromideHCID 61147—
Reactant1-(2-Pyridyl)piperazineHCID 94459—
SolventDichloromethaneHCID 6344—
Product2-Bromo-1-(4-pyridin-2-yl-piperazin-1-yl)-ethanoneHCID 63680031—

Reaction Conditions

Temperature0 °C

Reaction Steps

6.95 mL bromacetylbromide was dropped to 11.68 mL 1-pyridin-2-yl-piperazine and 11.23 mL triethylamine in 300 mL DCM at 0° C. The reaction was stirred 2 h at 0° C. The reaction mixture was added to water and extracted with DCM. The organic layer was dried with magesium sulfate and evaporated The residue was purified by chromatography on silica gel (DCM/MeOH 0-20%; 0.1% ammonia) to yield 23.6 g of the desired compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846948B2
Source datasetuspto-grants-2014_09
ORD IDord-12a5ad8dff734fa2988b238e32f0d3d1
Source noteuspto-grants-2014_09