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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1054764생성일: 2026년 10월 27일

Potassium Carbonate → 2-[4-(6-chloro-3-formyl-1H-indol-5-yl)phenoxy]-N-methylacetamide

https://huagongshe.com/reaction/1054764

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물2-(4-bromophenoxy)-N-methylacetamideHCID 7535023—
반응물methyl 6-chloro-5-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)-1H-indole-3-carboxylateHCID 86698665—
생성물2-[4-(6-chloro-3-formyl-1H-indol-5-yl)phenoxy]-N-methylacetamideHCID 8669875672.9%

반응 조건

온도90 °C

반응 단계

To the slurry of methyl-6-chloro-5-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)-1H-indole-3-carboxylate (240 mg, 1.0 mmol) was added 2 M potassium carbonate (2.5 mL, 5.0 mmol), 2-(4-bromophenoxy)-N-methylacetamide (240 mg, 1.00 mmol) and PddppfCl2 (50 mg, 0.061 mmol). The sealed vial was heated to 90° C. for 30 min. The reaction was cooled to room temperature and quenched with water (20 mL), and then washed three times with ethyl acetate (20 mL). The combined organics were dried and concentrated to give the title compound (250 mg, 55% yield) as a yellow solid that was used without further purification. 1H NMR (400 MHz, DMSO-d6) δ 9.94 (s, 1H), 8.37 (d, 1H), 8.02 (s, 1H), 7.68 (s, 1H), 7.38 (d, 2H), 7.05 (d, 2H), 4.52 (s, 2H), 2.68 (d, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09394285B2
출처 데이터셋uspto-grants-2016_07
ORD IDord-afc1d5eae2534beeb0de762c66178d6b
출처 메모uspto-grants-2016_07