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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 23874Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/23874

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPiperazineHCID 4837—
Edukt2-Benzenesulfonyl-5-chloropyridineHCID 10198940—
LösungsmittelPyridineHCID 1049—
ProduktPhenyl 5-(1-piperazinyl)-2-pyridinyl sulfoneHCID 983941848,3%

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06855709B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-8d80402db955440c94de8d01b68f81b7
Quellennotizuspto-grants-2005_02