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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1806264생성일: 2026년 10월 25일

Sodium Carbonate → 3-[1-(ethylsulfonyl)-4-piperidinyl]-5-[3-formyl-4,5-bis(methyloxy)phenyl]-1H-indole-7-carboxamide

https://huagongshe.com/reaction/1806264

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물5-Bromo-2,3-dimethoxybenzaldehydeHCID 322405—
반응물3-[1-(ethylsulfonyl)-4-piperidinyl]-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-7-carboxamideHCID 59828929—
촉매HCID 178418397HCID 178418397—
용매WaterHCID 962—
용매1,4-DioxaneHCID 31275—
생성물3-[1-(ethylsulfonyl)-4-piperidinyl]-5-[3-formyl-4,5-bis(methyloxy)phenyl]-1H-indole-7-carboxamideHCID 8663102659.1%

반응 조건

온도120 °C

반응 단계

To a solution of 3-[1-(ethylsulfonyl)-4-piperidinyl]-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-7-carboxamide (500 mg, 1.09 mmol) in dioxane (9.0 mL) and H2O (3.0 mL) was added sodium carbonate (690 mg, 6.51 mmol), and 5-bromo-2,3-bis(methyloxy)benzaldehyde (7.95 mg, 3.25 mmol). The reaction mixture was flushed under Argon for 10 min before addition of tetrakis(triphenylphosphine)palladium (0) (63 mg, 0.054 mmol). The reaction was then heated in a microwave at 120° C. for 30 min. All solvent was then concentrated and an aqueous wash was performed with EtOAc and H2O. The desired compound then precipitated and was filtered to give 322 mg of 3-[1-(ethylsulfonyl)-4-piperidinyl]-5-[3-formyl-4,5-bis(methyloxy)phenyl]-1H-indole-7-carboxamide (59%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08354406B2
출처 데이터셋uspto-grants-2013_01
ORD IDord-9d8c3fc9aa224bea984bdbb067fcbb17
출처 메모uspto-grants-2013_01