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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 911761생성일: 2026년 10월 26일

Phenol → 5-Chloro-3-phenoxy-2-pyridinamine

https://huagongshe.com/reaction/911761

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참여 물질

역할이름HCID투입량
반응물PhenolHCID 996—
반응물Cesium carbonateHCID 10796—
반응물3-Bromo-5-chloropyridin-2-amineHCID 2763971—
반응물SalicylaldoximeHCID 135408751—
촉매HCID 178419072HCID 178419072—
용매DimethylformamideHCID 6228—
생성물5-Chloro-3-phenoxy-2-pyridinamineHCID 1875287915%

반응 조건

온도110 °C

반응 단계

3-Bromo-5-chloropyridin-2-amine (50.0 g, 241 mmol), phenol (45.4 g, 482 mmol), copper(I)oxide (1.72 g, 12.1 mmol), (E)-2-hydroxybenzaldehyde oxime (6.61 g, 48.2 mmol), Cs2CO3 (157 g, 482 mmol), and 3A powdered molecular (72.3 g) sieves were placed in DMF (300 mL) and heated at 110° C. for 3 days. Reaction was cooled, then filtered through celite. Reaction was then partitioned between water and ether. An emulsion was formed and was filtered through a plug of celite. Water was extracted with ether then dried, filtered, and concentrated. Crude material was purified on a first silica gel chromatography (5-10% EtOAc in hexanes), and then on a second column to provide the title compound (8.00 g, 15.0% yield). 1H NMR (CDCl3) δ 7.80 (d, 1H), 7.39 (t, 2H), 7.19 (t, 1H), 7.03 (d, 2H), 6.94 (d, 1H), 4.76 (bs, 2H); Mass spectrum (apci) m/z=221 (100).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08022223B2
출처 데이터셋uspto-grants-2011_09
ORD IDord-fcc173c00df54cbb8c51834876f9afeb
출처 메모uspto-grants-2011_09