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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2266448생성일: 2026년 10월 27일

Potassium Carbonate → Trifluoromethanesulfonic Acid 7-chloro-3-(4-chlorobenzyl)-2,4-dimethylquinolin-5-yl Ester

https://huagongshe.com/reaction/2266448

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Phenyl triflimideHCID 142176—
반응물Trifluoromethanesulfonic acid 5-chloro-3-(4-chlorobenzyl)-2,4-dimethylquinolin-7-yl esterHCID 86631432—
반응물7-Chloro-3-(4-chlorobenzyl)-2,4-dimethylquinolin-5-olHCID 136335902—
반응물5-Chloro-3-(4-chlorobenzyl)-2,4-dimethylquinolin-7-olHCID 136335922—
용매TetrahydrofuranHCID 8028—
생성물Trifluoromethanesulfonic Acid 7-chloro-3-(4-chlorobenzyl)-2,4-dimethylquinolin-5-yl EsterHCID 86631431—

반응 조건

온도130 °C

반응 단계

A mixture of 7-chloro-3-(4-chlorobenzyl)-2,4-dimethylquinolin-5-ol and 5-chloro-3-(4-chlorobenzyl)-2,4-dimethylquinolin-7-ol (0.66 g), N-phenyltrifluoromethanesulfonimide (0.86 g), potassium carbonate (0.82 g) and tetrahydrofuran (10 mL) was heated by microwave irradiation at 130° C. for 20 minutes. The mixture was filtered and the filtrate concentrated under reduced pressure. Purification of the residue by column chromatography on silica gel, eluting with 1,2-dichloroethane gave a 50:50 mixture of title compound and trifluoromethanesulfonic acid 5-chloro-3-(4-chlorobenzyl)-2,4-dimethylquinolin-7-yl ester as a honey coloured gum, 0.86 g.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07858640B2
출처 데이터셋uspto-grants-2010_12
ORD IDord-1a6334b0f3044ab198c2a4144dd70497
출처 메모uspto-grants-2010_12