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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23874Generated: October 25, 2026

Piperazine → Phenyl 5-(1-piperazinyl)-2-pyridinyl sulfone

https://huagongshe.com/reaction/23874

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
Reactant2-Benzenesulfonyl-5-chloropyridineHCID 10198940—
SolventPyridineHCID 1049—
ProductPhenyl 5-(1-piperazinyl)-2-pyridinyl sulfoneHCID 983941848.3%

Reaction Conditions

Temperature120 °C

Reaction Steps

To a mixture of 5-chloro-2-pyridinyl phenyl sulfone (10.2 g, 40.2 mmol) in pyridine (100 mL) was added piperazine (13.8 g, 161 mmol). The mixture was heated to 120° C. in a preheated oil bath for 18 h. The mixture then was removed from heat and cooled to room temperature. The mixture was partitioned between water and ethyl acetate. The layers were separated and the organic layer washed twice with water (2×50 mL). The organic layer was dried with anhydrous magnesium sulfate and concentrated. The solids obtained after concentration were recrystallized from water and dried to give 5.89 g of the title compound; m.p. 126-127° C.; IR (drift) 1568, 1479, 1447, 1306, 1290, 1254, 1175, 1154, 1145, 1104, 830, 756, 715, 688, 602 cm−1. 1H NMR (CDCl3) δ 3.0, 3.29, 7.13, 7.53, 8.01, 8.26.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06855709B2
Source datasetuspto-grants-2005_02
ORD IDord-8d80402db955440c94de8d01b68f81b7
Source noteuspto-grants-2005_02