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HRID 1918642作成日:2026年10月27日

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

https://huagongshe.com/reaction/1918642

反応式

関与物質

役割名称HCID仕込み量
反応物Carbon tetrabromideHCID 11205—
反応物TriphenylphosphineHCID 11776—
反応物1H-Pyrrolo[2,3-B]pyridine-3-ethanol, 5-chloro-2-(triethylsilyl)-HCID 11056023—
溶媒TetrahydrofuranHCID 8028—
生成物3-(2-bromoethyl)-5-chloro-2-(triethylsilyl)-1H-pyrrolo[2,3-b]pyridineHCID 6683197145%

反応手順

Carbon tetrabromide (3.27 g, 9.65 mmol) was added to the solution of triphenylphosphine (2.56 g; 9.65 mmol) in THF (30 ml). The mixture was stirred at room temperature for 30 min. To this green suspension was added a solution of 2-(5-chloro-2-(triethylsilyl)-1H-pyrrolo[2,3-b]pyridin-3-yl)ethanol (2.00 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 crude material was purified by flash chromatography (eluent: 5 to 40% of ethyl acetate in heptanes) to give 1.08 g (45%) of 3-(2-bromoethyl)-5-chloro-2-(triethylsilyl)-1H-pyrrolo[2,3-b]pyridine as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08618138B2
出典データセットuspto-grants-2013_12
ORD IDord-c74a7a6237df4a35a9fc2e3ce6f077ed
出典メモuspto-grants-2013_12