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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 40918생성일: 2026년 10월 25일

Pyridine → 3-[3-(1-[2-(trimethylsilyl)ethoxy]methyl-1H-pyrrolo[2,3-b]pyridin-4-yl)-1,2,4-oxadiazol-5-yl]benzonitrile

https://huagongshe.com/reaction/40918

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물3-Cyanobenzoyl chlorideHCID 308483—
반응물HCID 178504228HCID 178504228—
용매AcetonitrileHCID 6342—
생성물3-[3-(1-[2-(trimethylsilyl)ethoxy]methyl-1H-pyrrolo[2,3-b]pyridin-4-yl)-1,2,4-oxadiazol-5-yl]benzonitrileHCID 5747766195.8%

반응 조건

온도80 °C

반응 단계

The crude product N-hydroxy-1-[2-(trimethylsilyl)ethoxy]methyl-1H-pyrrolo[2,3-b]pyridine-4-carboximidamide (0.06 gm, 0.0002 mol) was dissolved in pyridine (1.0 mL, 0.012 mol) and then 3-cyanobenzoyl chloride (0.040 g, 0.00024 mol) was added at rt. This mixture was stirred for 1 h and heated to 80° C. in an oil bath. After heating for 18 h the reaction was allowed to cool to rt and then diluted with ACN and concentrated in vacuo to give 3-[3-(1-[2-(trimethylsilyl)ethoxy]methyl-1H-pyrrolo[2,3-b]pyridin-4-yl)-1,2,4-oxadiazol-5-yl]benzonitrile 0.08 gm as an off white residue, LC/MS (M+H)+ 418.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08530485B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-ac254a0b10274bd3b2a0d14446a7ea0e
출처 메모uspto-grants-2013_09