돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 494264생성일: 2026년 10월 24일

Sodium Carbonate → N-Quinolin-7-yl-6-(4-trifluoromethylphenyl)-nicotinamide

https://huagongshe.com/ko/reaction/494264

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물4-(Trifluoromethyl)phenylboronic acidHCID 2734389—
반응물6-Chloro-N-quinolin-7-yl-nicotinamideHCID 44578987—
촉매HCID 178418397HCID 178418397—
용매1,2-DimethoxyethaneHCID 8071—
용매Ethyl AcetateHCID 8857—
생성물N-Quinolin-7-yl-6-(4-trifluoromethylphenyl)-nicotinamideHCID 44578937—

반응 단계

To a solution of 6-chloro-N-quinolin-7-yl-nicotinamide (D70) (40 mg, 0.14 mmol) in DME (0.9 ml) under an argon atmosphere was added 4-trifluoromethylphenylboronic acid (33 mg, 0.17 mmol), 2M sodium carbonate solution (0.17 ml) and tetrakis(triphenylphosphine)palladium (0) (8 mg, 0.007 mmol). The reaction was heated at reflux until complete by tlc, then cooled to room temperature and diluted with EtOAc and dried over MgSO4. The solvent was removed in vacuo and the resultant crude product was purified by SPE column chromatography. Elution with 75% EtOAc in 40-60° C. petroleum ether gave the title compound as an off-white solid. 1H NMR (250 MHz, CDCl3) δ (ppm): 9.31 (dd, 1H), 8.83 (dd, 1H), 8.46 (dd, 1H), 8.39 (dd, 1H), 8.20 (m, 3H), 8.07 (d, 1H), 7.94 (dd, 1H), 7.89 (d, 1H), 7.79 (d, 2H), 7.40 (dd, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07538121B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-3804f545fe4b4c91a07d363bb8bdb01c
출처 메모uspto-grants-2009_05