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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 587452생성일: 2026년 10월 24일

3-(2,3-dihydro-1H-indol-5-yl)-1-ethyl-1,3-dihydro-2H-imidazo[4,5-b]pyridin-2-one → HCID 58577674, 화합물

https://huagongshe.com/ko/reaction/587452

반응식

참여 물질

역할이름HCID투입량
반응물3-(2,3-dihydro-1H-indol-5-yl)-1-ethyl-1,3-dihydro-2H-imidazo[4,5-b]pyridin-2-oneHCID 58577282—
반응물2-Chloro-1-[[2-(trimethylsilanyl)ethoxy]methyl]-benzimidazoleHCID 59752898—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물HCID 58577674HCID 58577674—

반응 조건

온도120 °C

반응 단계

A mixture of 3-(2,3-dihydro-1H-indol-5-yl)-1-ethyl-1,3-dihydro-2H-imidazo[4,5-b]pyridin-2-one obtained from example 13e) and 2-chloro-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-benzimidazole (108 mg) in NMP (2.0 mL) was stirred at 120° C. for 12 h, treated with sat.NaHCO3aq. and extracted with AcOEt. The organic layer was dried over MgSO4 and concentrated in vacuo. The residue was purified by preparative HPLC and crystallized from AcOEt/Hexane to give 3-[1-(1H-benzimidazol-2-yl)-2,3-dihydro-1H-indol-5-yl]-1-ethyl-1,3-dihydro-2H-imidazo[4,5-b]pyridin-2-one (12 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09226921B2
출처 데이터셋uspto-grants-2016_01
ORD IDord-b7448e689c7e4368ada9fc656bddba5f
출처 메모uspto-grants-2016_01