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HRID 56221作成日:2026年10月25日

Acetamide → 3-(3-fluoro-4-((3-(tetrahydrofuran-2-yl)propyl)amino)phenyl)-2,6-dimethyl-pyrimidin-4(3H)-one

https://huagongshe.com/reaction/56221

反応式

関与物質

役割名称HCID仕込み量
反応物AcetamideHCID 178—
反応物O-XyleneHCID 7237—
反応物Ammonium ChlorideHCID 25517—
反応物N-(3-fluoro-4-((3-(tetrahydrofuran-2-yl)propyl)amino)phenyl)-3-oxobutan-amideHCID 90022774—
触媒Titanium isopropoxideHCID 11026—
溶媒TolueneHCID 1140—
生成物3-(3-fluoro-4-((3-(tetrahydrofuran-2-yl)propyl)amino)phenyl)-2,6-dimethyl-pyrimidin-4(3H)-oneHCID 9002293629.7%

反応条件

温度165 °C

反応手順

A mixture of N-(3-fluoro-4-((3-(tetrahydrofuran-2-yl)propyl)amino)phenyl)-3-oxobutanamide (250 mg, 0.78 mmol), acetamide (92 mg, 1.56 mmol), titanium tetraisopropanolate (1.9 mL) and xylene (10 mL) was stirred at 165° C. for 24 h. The mixture was then cooled to rt. 60 mL of toluene and 60 mL of saturated NH4Cl aqueous solution were added and the resulting mixture was stirred further at rt overnight. The mixture was then filtered and the filtrate was extracted with DCM (15 mL×3). The combined organic layers were washed with brine (15 mL×2), dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by a silica gel column chromatography (PE/EtOAc (V/V)=1:2) to give the title compound as a yellow solid (80 mg, 29%). The compound was characterized by the following spectroscopic data:

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09434695B2
出典データセットuspto-grants-2016_09
ORD IDord-3dbf39e8ebda4244a9c3ea891f60787c
出典メモuspto-grants-2016_09