Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 269481생성일: 2026년 10월 24일
2-Pyridineacetic acid, hydrochloride (1:1) → 2-Pyridin-2-yl-1-(1H-pyrrolo[2,3-b]pyridin-3-yl)-ethanone
https://huagongshe.com/ko/reaction/269481
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 2-Pyridineacetic acid, hydrochloride (1:1) | HCID 85317 | — |
| 반응물 | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| 반응물 | methyl 1H-pyrrolo[2,3-b]pyridine-3-carboxylate | HCID 21110084 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-Pyridin-2-yl-1-(1H-pyrrolo[2,3-b]pyridin-3-yl)-ethanone | HCID 59832245 | — |
반응 단계
To a solution of 1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid methyl ester (200 mg, 1.13 mmol) and 2-pyridinyl-acetic acid hydrochloride (440 mg, 2.53 mmol) in anhydrous THF (10 mL) was added LiHMDS (1.0 M in THF, 10 mL, 10.0 mmol) at −78° C. The solution was stirred at −78° C. for 30 min and was allowed to warm up to RT. After stirring at RT for another 30 min, the reaction mixture was heated under reflux for 14 h. The solvent was then evaporated, the residue was taken up to ethyl acetate (50 mL), and washed with aq. NaHCO3. The organic layer was dried over MgSO4, filtered, and evaporated. The residue was used directly for the next reaction.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07446199B2 |
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| 출처 데이터셋 | uspto-grants-2008_11 |
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| ORD ID | ord-ebe10ceb71664519a80050fdc239dbbd |
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| 출처 메모 | uspto-grants-2008_11 |
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