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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 44909생성일: 2026년 10월 24일

Dimethylformamide → 4-bromo-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-pyrrolo[2,3-b]pyridine

https://huagongshe.com/ko/reaction/44909

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Sodium hydrideHCID 24758—
반응물2-Chloromethyl 2-(trimethylsilyl)ethyl etherHCID 2724271—
반응물4-Bromo-1H-pyrrolo[2,3-b]pyridineHCID 22273643—
용매tert-Butyl methyl etherHCID 15413—
생성물4-bromo-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-pyrrolo[2,3-b]pyridineHCID 57477561139%

반응 단계

To a solution of 4-bromo-1H-pyrrolo[2,3-b]pyridine (6.2 g, 0.031 mol) and [β-(trimethylsilyl)ethoxy]methyl chloride (6.7 mL, 0.038 mol) in DMF (62 mL, 0.80 mol) was added sodium hydride (1.5 g, 0.038 mol) at 0° C., and the resulting solution turned opaque. The mixture was stirred for additional 4 h, then diluted with methyl tert-butyl ether (MTBE). The organic layer was separated and washed with water (×2) and brine aqueous solution successively. The organic phase was dried and concentrated in vacuo to give 14.1 g of a product as a pale orange oil. The oil was purified by column chromatography eluting with 5-20% ethyl acetate/hexanes to give the purified product as a colorless oil (9.66 g, 94% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541425B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-1f525b4d2f1b4256a7ea90f726007cf3
출처 메모uspto-grants-2013_09