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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1806211생성일: 2026년 10월 25일

Ethyl Acetate → 3-[1-(ethylsulfonyl)-4-piperidinyl]-5-(4-formyl-2-thienyl)-1H-indole-7-carboxamide

https://huagongshe.com/reaction/1806211

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물Potassium CarbonateHCID 11430—
반응물5-Bromothiophene-3-carbaldehydeHCID 12284894—
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—
용매MethanolHCID 887—
용매WaterHCID 962—
용매1,4-DioxaneHCID 31275—
생성물3-[1-(ethylsulfonyl)-4-piperidinyl]-5-(4-formyl-2-thienyl)-1H-indole-7-carboxamideHCID 57732828161.8%

반응 단계

To a solution of 5-bromo-3-thiophenecarbaldehyde (250 mg, 1.29 mmol) in dioxane (4.5 mL) and H2O (1.5 mL) was added 3-[1-(ethylsulfonyl)-4-piperidinyl]-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-7-carboxamide (200 mg, 0.43 mmol), potassium carbonate (250 mg, 2.58 mmol) and tetrakis(triphenylphosphine)palladium (0) (56 mg, 0.049 mmol). The reaction was run in the microwave at 150° C. for 20 min. It was then treated with EtOAc and H2O to obtain the crude product. This was then treated with MeOH (10 mL) and the solid was filtered and collected to give 310 mg of the desired title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08354406B2
출처 데이터셋uspto-grants-2013_01
ORD IDord-c32ef290e0714211b7fd8600754abfb5
출처 메모uspto-grants-2013_01