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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1012660생성일: 2026년 10월 27일

Potassium Carbonate → 2-{3-[2-Chloro-4-(4-chloro-2-methyl-phenylamino)-benzoyl]-4-fluoro-phenoxy}-N-methyl-acetamide

https://huagongshe.com/reaction/1012660

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참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물2-chloro-N-methylacetamideHCID 66773—
반응물[2-Chloro-4-(4-chloro-2-methyl-phenylamino)-phenyl]-(2-fluoro-5-hydroxy-phenyl)-methanoneHCID 67313338—
용매AcetonitrileHCID 6342—
생성물2-{3-[2-Chloro-4-(4-chloro-2-methyl-phenylamino)-benzoyl]-4-fluoro-phenoxy}-N-methyl-acetamideHCID 58677531—

반응 조건

온도130 °C

반응 단계

Compound 513 (36 mg, 0.09 mmol) was dissolved in acetonitrile (2 mL) in a reaction vial. 2-Chloro-N-methyl-acetamide (30 mg, 0.28 mmol), K2CO3 (38 mg, 0.28 mmol) were added. The reaction vial was flushed with argon, closed and then stirred at 130° C. for 45 min. in a microwave oven. The reaction mixture was poured into a mixture of EtOAc:H2O (1:1, 10 mL). The layers were separated and the aqueous phase was extracted with EtOAc (3×5 mL). The combined organic layers were dried (MgSO4), filtered, concentrated in vacuo and purified by continuously gradient flash chromatography using EtOAc/petroleum ether (40-60)(v:v=1:3 to 100:0) as the eluent, affording the title compound as a yellow oil. 13C NMR (CDCl3) δ 190.1, 168.2, 155.7 (d), 153.2 (d), 149.2, 136.6, 135.0, 134.5, 133.4, 131.2, 130.5, 128.7 (d), 128.1, 127.1, 125.3, 119.6 (d), 117.4 (d), 116.1 (d), 115.6, 112.4, 68.0, 25.8, 17.9

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07977387B2
출처 데이터셋uspto-grants-2011_07
ORD IDord-394ec7c6d0e64cae974394d43fad958c
출처 메모uspto-grants-2011_07