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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 550891생성일: 2026년 10월 26일

Methane → ethyl 3-(4-aminophenyl)-1H-pyrrolo[2,3-c]pyridine-2-carboxylate

https://huagongshe.com/reaction/550891

반응식

참여 물질

역할이름HCID투입량
반응물MethaneHCID 297—
반응물Potassium FluorideHCID 522689—
반응물(4-Aminophenyl)boronic acid hydrochlorideHCID 2734614—
반응물ethyl 3-bromo-1H-pyrrolo[2,3-c]pyridine-2-carboxylateHCID 57445353—
촉매HCID 178418397HCID 178418397—
용매WaterHCID 962—
용매TriethylamineHCID 8471—
용매1,4-DioxaneHCID 31275—
생성물ethyl 3-(4-aminophenyl)-1H-pyrrolo[2,3-c]pyridine-2-carboxylateHCID 5744535257.4%

반응 단계

To a solution of 1 g of ethyl 3-bromo-1H-pyrrolo[2,3-c]pyridine-2-carboxylate in 100 mL of dioxane are added 773 mg of 4-aminophenylboronic acid hydrochloride and 1.1 g of potassium fluoride in 9 mL of water. The reaction mixture is stirred under an argon atmosphere for 15 minutes. 425 mg of tetrakis(triphenylphosphine)palladium(0) and 630 μL of triethylamine are added. The reaction mixture is stirred for 17 hours at reflux. After treating with carbon black and then filtering through Celite®, the filtrate is concentrated under reduced pressure. The residue is purified by flash chromatography on a column of silica (60; 35-70 μM), eluting with a mixture of dichloromethane, methanol and acetonitrile (90/5/5 by volume). 600 mg of ethyl 3-(4-aminophenyl)-1H-pyrrolo[2,3-c]pyridine-2-carboxylate are obtained, the characteristics of which are as follows:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07947706B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-cb85bc5963f54265acc359ec33f26a0a
출처 메모uspto-grants-2011_05