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HRID 246481생성일: 2026년 10월 26일

Sodium hydride → 7-bromo-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrolo[2,3-c]pyridine

https://huagongshe.com/reaction/246481

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참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물2-Chloromethyl 2-(trimethylsilyl)ethyl etherHCID 2724271—
반응물7-Bromo-6-azaindoleHCID 19696456—
용매DimethylformamideHCID 6228—
생성물7-bromo-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrolo[2,3-c]pyridineHCID 8667798284%

반응 조건

온도25 °C

반응 단계

To a stirred solution of 7-bromo-1H-pyrrolo[2,3-c]pyridine (0.2 g, 1.02 mmol) in DMF (5 mL), cooled to 0° C., was added sodium hydride (46.7 mg, 1.17 mmol). After 10 min the mixture was warmed to 25° C. After 20 min the mixture was recooled to 0° C. and (2-(chloromethoxy)ethyl)trimethylsilane (186 mg, 1.12 mmol) added drop-wise. After 5 min the mixture was warmed to 25° C. After 20 min the mixture was partitioned between ethyl acetate and water. The organic phase was washed with water then concentrated in vacuo. Purification by chromatography (silica, 12 g Analogix column, 0-8% ethyl acetate in hexanes) gave 7-bromo-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrolo[2,3-c]pyridine (0.28 g, 84%) as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08658646B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-78677bea67a646aa9ba29b4b70cfdefe
출처 메모uspto-grants-2014_02