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HRID 2113718作成日:2026年10月23日

Trifluoroacetic acid → 3-ethyl-6-fluoro-1-(tetrahydro-2H-pyran-4-yl)-1H-pyrazolo[3,4-b]pyridine

https://huagongshe.com/ja/reaction/2113718

反応式

関与物質

役割名称HCID仕込み量
反応物Trifluoroacetic acidHCID 6422—
反応物N'-(oxan-4-yl)(tert-butoxy)carbohydrazideHCID 45092245—
反応物1-(2,6-Difluoropyridin-3-YL)propan-1-oneHCID 53413972—
溶媒DichloromethaneHCID 6344—
生成物3-ethyl-6-fluoro-1-(tetrahydro-2H-pyran-4-yl)-1H-pyrazolo[3,4-b]pyridineHCID 5981079183.9%

反応条件

温度75 °C

反応手順

A mixture of tert-butyl 2-(tetrahydro-2H-pyran-4-yl)hydrazinecarboxylate (3.8 g, 0.018 mol) and trifluoroacetic acid (20 mL, 0.3 mol) were stirred in dichloromethane (20 mL) for 90 minutes. The mixture was concentrated, and the residue was taken up in acetonitrile (30 mL). 1-(2,6-difluoropyridin-3-yl)propan-1-one (2.34 g, 0.0137 mol) was then added, and the resulting mixture was stirred at 75° C. for 72 hours. After cooling to room temperature, the mixture was concentrated, and the residue was purified by flash chromatography on silica gel using a 10-50% hexane:ethyl acetate gradient (flow rate 20 mL/min). The organics were combined and the crude product was then extracted with ethyl acetate. The combined extracts were washed with saturated sodium bicarbonate and then concentrated to afford 2.86 g (83.9%) of 3-ethyl-6-fluoro-1-(tetrahydro-2H-pyran-4-yl)-1H-pyrazolo[3,4-b]pyridine as a white solid. LC/MS (EI) tR 3.5 (Method E), m/z 250 (M++1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07432266B2
出典データセットuspto-grants-2008_10
ORD IDord-2ce04c67934041968403a7312ecb8594
出典メモuspto-grants-2008_10