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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 336359Generated: October 27, 2026

Triethylamine → 2-Bromo-1-(4-pyrimidin-2-ylpiperazin-1-yl)ethanone

https://huagongshe.com/reaction/336359

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBromoacetyl bromideHCID 61147—
Reactant1-(2-Pyrimidinyl)piperazineHCID 88747—
SolventTetrahydrofuranHCID 8028—
Product2-Bromo-1-(4-pyrimidin-2-ylpiperazin-1-yl)ethanoneHCID 636798460.1%

Reaction Steps

20.2 g bromacetylbromide was dropped to 16.5 g 1-pyrimidin-2-yl-piperazin and 10.2 g triethylamine in 250 mL THF. The reaction was stirred over night at RT and evaporated. The residue was extracted with DCM and water. The organic layer was evaporated and the residue was crystallized with petrolether and then purified by chromatography on silica gel (DCM/MeOH:95/5) to yield 36 mg of the desired compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889677B2
Source datasetuspto-grants-2014_11
ORD IDord-df1e764b7f984c31996312bf9931eef1
Source noteuspto-grants-2014_11