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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 523149생성일: 2026년 10월 25일

Cesium fluoride → 4-Chloro-6-(4-isopropoxyphenyl)-6'-methoxy-2,2'-bipyridine

https://huagongshe.com/reaction/523149

반응식

참여 물질

역할이름HCID투입량
반응물Cesium fluorideHCID 25953—
반응물2-Methoxy-6-(tributylstannyl)pyridineHCID 10524891—
반응물2,4-Dichloro-6-(4-isopropoxyphenyl)pyridineHCID 90118079—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매HCID 178418397HCID 178418397—
생성물4-Chloro-6-(4-isopropoxyphenyl)-6'-methoxy-2,2'-bipyridineHCID 9011807192%

반응 단계

To a 2 dram vial equipped with a stir bar was added 2,4-dichloro-6-(4-isopropoxyphenyl)pyridine (50 mg, 0.18 mmol), 2-methoxy-6-(tributylstannyl)pyridine (701 mg, 0.178 mmol), CuI (9 mg, 0.05 mmol), CsF (82 mg, 0.54 mmol), and Pd(PPh3)4 (10 mg, 8.9 μmol). The vial was sealed with a septum screw-cap and then placed under N2 atmosphere. To the vial was added degassed DMF (1 mL). The vial was placed in a 80° C. heating block with stirring for 1 hour. The reaction mixture was allowed to cool to room temperature and was then directly purified via C18 chromatography (water:MeOH w/0.1% TFA) to afford 4-chloro-6-(4-isopropoxyphenyl)-6′-methoxy-2,2′-bipyridine as a dark solid (58 mg, 92%). 1H-NMR (500 MHz, CDCl3) 8.29 (d, J=1.7 Hz, 1H), 8.21 (dd, J=7.4, 0.5 Hz, 1H), 8.09-8.04 (m, 2H), 7.74 (t, J=7.8 Hz, 1H), 7.67 (d, J=1.7 Hz, 1H), 7.03-6.99 (m, 2H), 6.82 (dd, J=8.2, 0.5 Hz, 1H), 4.66 (spt, J=6.1 Hz, 1H), 4.08 (s, 3H), 1.40 (d, J=6.0 Hz, 6H); MS: MS m/z 355.2 (M++1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09334279B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-1b7d81763f1d4f90aafef7b4a53da1c4
출처 메모uspto-grants-2016_05