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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972368Generated: October 25, 2026

Triethylamine → 5-Bromo-2-(4-(phenylsulfonyl)-1-piperazinyl)pyrimidine

https://huagongshe.com/reaction/1972368

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1,4-DioxaneHCID 31275—
Reactant5-Bromo-2-chloropyrimidineHCID 606665—
Reactant1-(Benzenesulfonyl)piperazine hydrochlorideHCID 2756581—
SolventWaterHCID 962—
Product5-Bromo-2-(4-(phenylsulfonyl)-1-piperazinyl)pyrimidineHCID 3966061450.5%

Reaction Steps

A 250 mL round-bottomed flask was charged with 1-(phenylsulfonyl)piperazine hydrochloride (4.08 g, 15.51 mmol, Example 15, step 1), 5-bromo-2-chloropyrimidine (2.50 g, 12.92 mmol, Sigma-Aldrich, St. Louis, Mo.), and 20 mL of dioxane. To this was added triethylamine (4.50 mL, 32.3 mmol). After stirring at room temperature for 3 h, the mixture was diluted with water (50 mL) and the resulting precipitate was collected by filtration to give 5-bromo-2-(4-(phenylsulfonyl)-1-piperazinyl)pyrimidine (2.50 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431563B2
Source datasetuspto-grants-2013_04
ORD IDord-143ebc81d7de4196acfd56839e71b66e
Source noteuspto-grants-2013_04