Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 85036생성일: 2026년 10월 26일
1H-Pyrrolo(2,3-b)pyridine → 1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrolo[2,3-b]pyridine
https://huagongshe.com/reaction/85036
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1H-Pyrrolo(2,3-b)pyridine | HCID 9222 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 2-Chloromethyl 2-(trimethylsilyl)ethyl ether | HCID 2724271 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrolo[2,3-b]pyridine | HCID 58431351 | 100.6% |
반응 단계
To a stirred solution of 7-azaindole (1.18 g, 10.0 mmol) in anhydrous dimethylformamide (10 mL) cooled to 0° C. was added NaH [60% dispersion in mineral oil](0.480 g, 12.0 mmol) in portions over 15 min. The resulting mixture was allowed to stir for 1 hr at 0° C., after which (2-(chloromethoxy)ethyl)trimethylsilane [SEM-Cl] (2.12 mL, 12.0 mmol) was added over 15 min. The resulting mixture was stirred for 1 hr, after which it was quenched with H2O (50 mL), and partioned between EtOAc and H2O. The organic layer was separated, washed with brine, dried over MgSO4, filtered, and evaporated in vacuo to yield a yellow oil (2.50 g, 100%). HPLC retention time: 2.66 minutes; MS ESI (m/z): 249.4 (M+1)+, calc. 248.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08846909B2 |
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| 출처 데이터셋 | uspto-grants-2014_09 |
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| ORD ID | ord-91f4e083c1914a8784c70848a1633c2b |
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| 출처 메모 | uspto-grants-2014_09 |
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