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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 494067생성일: 2026년 10월 25일

Hydrochloric Acid → 3-cyclohexyl-N-(N,N-dimethylsulfamoyl)-2-(2-formyl-4-methoxyphenyl)-1H-indole-6-carboxamide

https://huagongshe.com/reaction/494067

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Potassium CarbonateHCID 11430—
반응물Boronic AcidHCID 61668—
반응물2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
반응물2-bromo-3-cyclohexyl-N-(dimethylsulfamoyl)-1H-indole-6-carboxamideHCID 58765150—
촉매palladium(II) acetateHCID 167845—
용매WaterHCID 962—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물3-cyclohexyl-N-(N,N-dimethylsulfamoyl)-2-(2-formyl-4-methoxyphenyl)-1H-indole-6-carboxamideHCID 59750076—

반응 단계

A mixture of the 2-Bromo-3-cyclohexyl-N-[(dimethylamino)sulfonyl]-1H-indole-6-carboxamide (4.28 g, 0.01 mol), boronic acid (2.7 g, 0.015 mol), 2-dicyclohexylphosphino-2′,6′-dimethoxy-biphenyl (41 mg, 0.0001 mol), palladium acetate (11.2 mg), and finely ground potassium carbonate (4.24 g, 0.02 mol) in toluene (30 mL) was stirred under reflux and under nitrogen for 30 min, at which time LC/MS analysis showed the reaction to be complete. The reaction mixture was then diluted with ethyl acetate and water, and then acidified with an excess of dilute HCl. The ethyl acetate layer was then collected and washed with dilute HCl, water and brine. The organic solution was then dried (magnesium sulfate), filtered and concentrated to give a gum. The gum was diluted with hexanes (250 ml) and ethyl acetate (25 mL), and the mixture was stirred for 20 hr at 22° C. during which time the product was transformed into a bright yellow granular solid (4.8 g) which was used directly without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07538102B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-a1db0a003b2544b4808b01a6f4046d9d
출처 메모uspto-grants-2009_05