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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 218852생성일: 2026년 10월 24일

Potassium Carbonate → 7-isopropoxy-6-Methoxy-2-methyl-3-(3,4,5-trimethoxybenzoyl)-1H-indole

https://huagongshe.com/ko/reaction/218852

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물5-Iodo-1,2,3-trimethoxybenzeneHCID 298133—
반응물2-isopropoxy-3-methoxy-6-(prop-1-ynyl)-N-trifluoroacetylanilineHCID 86637656—
생성물7-isopropoxy-6-Methoxy-2-methyl-3-(3,4,5-trimethoxybenzoyl)-1H-indoleHCID 6728671864%

반응 단계

A mixture of the product of Step C (0.171 g; 0.54 mmol), 3,4,5-trimethoxyphenyl iodide (0.191 g; 0.65 mmol), Cl2Pd(PPh3)2 (0.044 g; 0.063 mmol); dry K2CO3 (0.23 g; 1.62 mmol in anhydrous DMF (5 ml) was degassed under reduced pressure and saturated with CO gas. The resulting mixture was vigorously stirred overnight at room temperature under CO balloon, then diluted to 50 ml with ethyl acetate and washed with water (3×15 ml), brine and dried over anhydrous MgSO4, filtered off and filtrate evaporated to dryness. The residue was purified by flash column chromatography (SiO2 CH2Cl2/ethyl acetate, 9:1) to give the title compound (0.143 g; 64% yield) as a yellow solid. 1H-NMR (CDCl3) 1.27 (d, 6H, J=6.14 Hz); 2.51 (s, 3H); 3.79 (s, 6H); 3.85 (s, 3H); 3.90 (s, 3H); 4.69 (m, 1H, J=6.14 Hz): 6.76 (d, 1H, J=8.75 Hz); 7.04 (s, 2H); 7.11 (d, 1H, J=8.75 Hz); 8.83 (broad m, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08198466B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-1bd161adf2334851bd68e86ec6efacc3
출처 메모uspto-grants-2012_06