Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1426546생성일: 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/1426546
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Pyridine | HCID 1049 | — |
| 반응물 | 3-Cyanobenzoyl chloride | HCID 308483 | — |
| 반응물 | HCID 178504228 | HCID 178504228 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 3-[3-(1-[2-(trimethylsilyl)ethoxy]methyl-1H-pyrrolo[2,3-b]pyridin-4-yl)-1,2,4-oxadiazol-5-yl]benzonitrile | HCID 57477661 | 95.8% |
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/M S (M+H)+ 418.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08933086B2 |
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| 출처 데이터셋 | uspto-grants-2015_01 |
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| ORD ID | ord-fd9abfb2476b4630a82ad0ba9fd15004 |
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| 출처 메모 | uspto-grants-2015_01 |
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