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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

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참여 물질

역할이름HCID투입량
반응물1H-Pyrrolo(2,3-b)pyridineHCID 9222—
반응물Sodium hydrideHCID 24758—
반응물2-Chloromethyl 2-(trimethylsilyl)ethyl etherHCID 2724271—
용매DimethylformamideHCID 6228—
생성물1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrolo[2,3-b]pyridineHCID 58431351100.6%

반응 조건

온도0 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846909B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-91f4e083c1914a8784c70848a1633c2b
출처 메모uspto-grants-2014_09