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HRID 7628作成日:2026年10月23日

Potassium Carbonate → 2-[7-(3-Fluoro-benzyloxy)-2-methyl-4-oxo-4H-quinazolin-3-yl]-acetamide

https://huagongshe.com/ja/reaction/7628

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物3-Fluorobenzylic alcoholHCID 68008—
反応物Methyl 4-fluoro-2-nitrobenzoateHCID 14941412—
反応物4-(3-Fluoro-benzyloxy)-2-nitro-benzoic acid methyl esterHCID 69594337—
反応物4-(3-Fluorobenzyloxy)-2-nitro-benzoic acid (3-fluoro-benzyl) esterHCID 86593646—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物2-[7-(3-Fluoro-benzyloxy)-2-methyl-4-oxo-4H-quinazolin-3-yl]-acetamideHCID 1002018076%

反応条件

温度65 °C

反応手順

4-(3-Fluoro-benzyloxy)-2-nitro-benzoic acid (3-fluoro-benzyl) ester and 4-(3-fluoro-benzyloxy)-2-nitro-benzoic acid methyl ester: A mixture of 4-fluoro-2-nitro-benzoic acid methyl ester (9.2 g, 46.3 mmol), 3-fluorobenzyl alcohol (16.7 g, 132.4 mmol) and potassium carbonate (12.8 g, 92.6 mmol) in DMF (210 mL) was heated at 65° C. for 48 h. After cooling to rt, the mixture was poured into water (400 mL), and extracted with diethyl ether (3×100 mL). The combined extracts were washed with brine (100 mL) dried and evaporated. Purification by chromatography on silica gel eluting with ethyl acetate:hexane (1:1) afforded the title compound (14.0 g, 76%) as a light yellow liquid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087612B2
出典データセットuspto-grants-2006_08
ORD IDord-f243056d574b4911b9c3d4786237c32f
出典メモuspto-grants-2006_08