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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 23874생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물PiperazineHCID 4837—
반응물2-Benzenesulfonyl-5-chloropyridineHCID 10198940—
용매PyridineHCID 1049—
생성물Phenyl 5-(1-piperazinyl)-2-pyridinyl sulfoneHCID 983941848.3%

반응 조건

온도120 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06855709B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-8d80402db955440c94de8d01b68f81b7
출처 메모uspto-grants-2005_02