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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1777582생성일: 2026년 10월 26일

Carbon tetrabromide → 3-(2-bromoethyl)-5-chloro-2-(triethylsilyl)-1H-pyrrolo[2,3-b]pyridine

https://huagongshe.com/reaction/1777582

반응식

참여 물질

역할이름HCID투입량
반응물Carbon tetrabromideHCID 11205—
반응물TriphenylphosphineHCID 11776—
반응물1H-Pyrrolo[2,3-B]pyridine-3-ethanol, 5-chloro-2-(triethylsilyl)-HCID 11056023—
용매TetrahydrofuranHCID 8028—
생성물3-(2-bromoethyl)-5-chloro-2-(triethylsilyl)-1H-pyrrolo[2,3-b]pyridineHCID 6683197145%

반응 단계

Carbon tetrabromide (3.27 g, 9.65 mmol) was added to a solution of triphenylphosphine (2.56 g; 9.65 mmol) in THF (30 mL). The mixture was stirred at room temperature for 30 minutes. To this green suspension was added a solution of 2-(5-chloro-2-(triethylsilyl)-1H-pyrrolo[2,3-b]pyridin-3-yl)ethanol (2 g; 6.43 mmol) in THF (20 mL) and the resulting reaction mixture was stirred for 20 hours. The precipitate was eliminated by filtration and the filtrate was concentrated under reduced pressure. The residue was purified by flash chromatography (eluent 5 to 40% ethyl acetate in heptane) to give 1.08 g (45%) of 3-(2-bromoethyl)-5-chloro-2-(triethylsilyl)-1H-pyrrolo[2,3-b]pyridine as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09266832B2
출처 데이터셋uspto-grants-2016_02
ORD IDord-d610fbfc39a14794985643cf250607fa
출처 메모uspto-grants-2016_02