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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 747576생성일: 2026년 10월 25일

Sodium Carbonate → 5-[1-(3-Thiophen-2-yl-phenyl)-ethylcarbamoyl]-thiophene-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/747576

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물2-Thiopheneboronic acidHCID 2733960—
반응물5-[1-(3-Bromo-phenyl)-ethylcarbamoyl]-thiophene-2-carboxylic acid methyl esterHCID 69292871—
촉매Tetrakis(triphenylphosphine)palladiumHCID 11979704—
용매EthanolHCID 702—
용매1,2-DimethoxyethaneHCID 8071—
생성물5-[1-(3-Thiophen-2-yl-phenyl)-ethylcarbamoyl]-thiophene-2-carboxylic acid methyl esterHCID 6929341280.1%

반응 단계

To a suspension of 10.0 mg (0.0086 mmol) tetrakis(triphenylphosphine)-palladium(0) in 2 ml dry dimethoxyethane, 100 mg (0.272 mmol) 5-[1-(3-Bromo-phenyl)-ethylcarbamoyl]-thiophene-2-carboxylic acid methyl ester were added and stirred for 10 min at room temperature under nitrogen atmosphere. 52.5 mg (0.410 mmol) thiophene-2-boronic acid in 0.5 ml ethanol and 285 μl (0.570 mmol) of a 2 M aqueous solution of Na2CO3 were added and the mixture was heated in the microwave oven (Emrys Optimizer) at 100° C. for 25 min. After cooling to room temperature, the reaction mixture was filtered and the solid was washed with ethanol. The solvent of the combined filtrates was evaporated. The residue was dissolved in ethyl acetate and washed with brine. The organic phase was dried over magnesium sulfate, the solvent was evaporated and the residue was subjected to silica gel chromatography (ethyl acetate/n-heptane 1:2) to yield 81 mg (0.218 mmol) 5-[1-(3-thiophen-2-yl-phenyl)-ethylcarbamoyl]-thiophene-2-carboxylic acid methyl ester.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07396944B2
출처 데이터셋uspto-grants-2008_07
ORD IDord-1e9ef8c9b69b458b8dc9fbbb9969b819
출처 메모uspto-grants-2008_07