戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1918641作成日:2026年10月26日

Sodium Carbonate → 1H-Pyrrolo[2,3-B]pyridine-3-ethanol, 5-chloro-2-(triethylsilyl)-

https://huagongshe.com/reaction/1918641

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物Lithium ChlorideHCID 433294—
反応物4-(Triethylsilyl)-3-butyn-1-olHCID 2760694—
反応物2-Amino-5-chloro-3-iodopyridineHCID 11076010—
触媒HCID 178478483HCID 178478483—
溶媒DimethylformamideHCID 6228—
生成物1H-Pyrrolo[2,3-B]pyridine-3-ethanol, 5-chloro-2-(triethylsilyl)-HCID 1105602388%

反応手順

A mixture of 5-chloro-3-iodopyridin-2-amine (2 g; 7.86 mmol), 4-(triethylsilyl)but-3-yn-1-ol (4.35 g; 23.58 mmol); (1,1′-bis(diphenylphosphino)ferrocene)-dichloromethane (0.321 g; 0.393 mmol), lithium chloride (0.333 g; 7.86 mmol) and sodium carbonate (1.67 g; 15.72 mmol) in DMF (15 mL) was heated at 100° C. for approximately 20 hours. After cooling, the mixture was concentrated under reduced pressure and the residue was partitioned between brine and ethyl acetate. After separation the organic layer was evaporated and the residue was purified by flash chromatography on silica gel (eluent 7 to 80% of ethyl acetate in heptane) to give 2.15 g (88%) of 2-(5-chloro-2-(triethylsilyl)-1H-pyrrolo[2,3-b]pyridin-3-yl)ethanol 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-4572b156eda04827b10f40a688a9287b
出典メモuspto-grants-2013_12