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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428934Generated: October 26, 2026

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

https://huagongshe.com/reaction/1428934

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 6367984631.2%

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 mixture was stirred overnight 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 8.9 g of the desired compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08937176B2
Source datasetuspto-grants-2015_01
ORD IDord-b4599b616dfb4990b055fba283194bfe
Source noteuspto-grants-2015_01