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HRID 56282作成日:2026年10月26日

Toluene → 3-(3-chloro-4-morpholinophenyl)-2-((3-chlorophenoxy)methyl)-6-methyl-pyrimidin-4(3H)-one

https://huagongshe.com/reaction/56282

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物Ammonium ChlorideHCID 25517—
反応物2-(3-Chlorophenoxy)acetamideHCID 2745969—
反応物N-(3-chloro-4-morpholinophenyl)-3-oxobutanamideHCID 90022603—
触媒Titanium isopropoxideHCID 11026—
溶媒O-XyleneHCID 7237—
生成物3-(3-chloro-4-morpholinophenyl)-2-((3-chlorophenoxy)methyl)-6-methyl-pyrimidin-4(3H)-oneHCID 9005170064%

反応条件

温度165 °C

反応手順

A mixture of N-(3-chloro-4-morpholinophenyl)-3-oxobutanamide (0.48 g, 1.62 mmol), 2-(3-chlorophenoxy)acetamide (0.60 g, 3.24 mmol) and titanium tetraisopropanolate (2.4 mL) in xylene (10 mL) was stirred at 165° C. for 24 h. The mixture was cooled to rt and 60 mL of toluene and 60 mL of saturated NH4Cl aqueous solution were added. The resulting mixture was stirred at rt overnight and filtered and the filtrate was extracted with DCM (20 mL×4). The combined organic layers were washed with brine (30 mL×2), dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by a silica gel column chromatography (PE/EtOAc (V/V)=1:1) to give the title compound as a yellow solid (0.46 g, 64%). 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-6dcbc20cf52e40a79ed93a3709ffb114
出典メモuspto-grants-2016_09