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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 562065생성일: 2026년 10월 26일

Potassium Carbonate → 3-[1-(ethylsulfonyl)-4-piperidinyl]-5-(2-fluoro-5-formylphenyl)-1H-indole-7-carboxamide

https://huagongshe.com/reaction/562065

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물3-Bromo-4-fluorobenzaldehydeHCID 173604—
반응물3-[1-(ethylsulfonyl)-4-piperidinyl]-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-7-carboxamideHCID 59828929—
용매WaterHCID 962—
용매1,4-DioxaneHCID 31275—
생성물3-[1-(ethylsulfonyl)-4-piperidinyl]-5-(2-fluoro-5-formylphenyl)-1H-indole-7-carboxamideHCID 86631020—

반응 조건

온도160 °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 (200 mg, 0.434 mmol) in dioxane (3.0 mL) and H2O (1.0 mL) was added 3-bromo-4-fluorobenzaldehyde (264 mg, 1.30 mmol), and K2CO3 (360 mg, 2.60 mmol) in microwave tube. The reaction mixture was degassed for 5 min before addition of tetrakis(triphenylphosphosphine) palladium (0) (48 mg, 0.043 mmol). The reaction was heated in a microwave for 30 min at 160° C. The organic layer was separated and concentrated. The residue was dissolved in MeOH until solid precipitated to yield 3-[1-(ethylsulfonyl)-4-piperidinyl]-5-(2-fluoro-5-formylphenyl)-1H-indole-7-carboxamide.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08063071B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-75e35c5310194506b83d7321ed44e967
출처 메모uspto-grants-2011_11