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HRID 69694作成日:2026年10月23日

4-Methylmorpholine → 3-chloro-4-fluoro-N-methylbenzamide

https://huagongshe.com/ja/reaction/69694

反応式

関与物質

役割名称HCID仕込み量
反応物4-MethylmorpholineHCID 7972—
反応物3-Chloro-4-fluorobenzoic acidHCID 520989—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物1-Hydroxybenzotriazole hydrateHCID 2796029—
反応物Methylamine hydrochlorideHCID 6364545—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物3-chloro-4-fluoro-N-methylbenzamideHCID 6011712453.1%

反応条件

温度23 °C

反応手順

To a suspension of 3-chloro-4-fluorobenzoic acid (25.0 g, 143 mmol), Methylamine hydrochloride (11.60 g, 172 mmol), N1-((ethylimino)methylene)-N3,N3-dimethylpropane-1,3-diamine hydrochloride (41.2 g, 215 mmol), and 1H-benzo[d][1,2,3]triazol-1-ol hydrate (32.9 g, 215 mmol) in DMF (Volume: 150 mL) was added 4-methylmorpholine (79 mL, 716 mmol) at 23° C. The reaction was stirred at 23° C. for 3 hr. The reaction mixture was diluted with water (500 mL) to furnish a yellow-orange solution. The solution was stirred overnight at 23° C. affording a suspension. The suspension was filtered, washed with H2O (3×100 mL), and the resulting solid was dried in vacuo at 30° C. to provide 3-chloro-4-fluoro-N-methylbenzamide (14.24 g, 76 mmol, 53.0% yield) as an off-white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 2.78 (d, J=4.55 Hz, 3 H) 7.53 (t, J=8.97 Hz, 1 H) 7.86 (ddd, J=8.59, 4.80, 2.27 Hz, 1 H) 8.04 (dd, J=7.20, 2.15 Hz, 1 H) 8.51-8.65 (m, 1 H). ESI-MS: m/z 188.0 (M+H)+. Mp=108.3-110.0° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822470B2
出典データセットuspto-grants-2014_09
ORD IDord-8004a225c1cc47d591d69c60bce8c2ca
出典メモuspto-grants-2014_09