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HRID 239992作成日:2026年10月26日

Triethylamine → Methyl 4-[[5-bromo-2-(trifluoromethyl)benzoyl]amino]-3,5-dimethyl-benzoate

https://huagongshe.com/reaction/239992

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Propylphosphonic anhydrideHCID 111923—
反応物Benzoic acid, 4-amino-3,5-dimethyl-, methyl esterHCID 11030398—
反応物5-Bromo-2-trifluoromethylbenzoic acidHCID 50998140—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物Methyl 4-[[5-bromo-2-(trifluoromethyl)benzoyl]amino]-3,5-dimethyl-benzoateHCID 8670737840.2%

反応手順

To a solution of 5-bromo-2-(trifluoromethyl)benzoic acid (1.00 g, 0.00371 mol) in CH2Cl2 (15 mL) at room temperature are added methyl 4-amino-3,5-dimethylbenzoate (0.46 g, 0.00260 mol, see preparation 12) and triethylamine (1.10 ml, 0.00743 mol). After stirring the reaction mixture for 10 minutes, 1-propanephosphonic acid cyclic anhydride (50% solution in ethyl acetate, 6.00 ml, 0.00929 mol) is added via syringe and stirred at room temperature. After 14 hours, the reaction mixture is diluted with water and extracted with dichloromethane. The organic layers are combined and dried over magnesium sulfate, filtered, and concentrated under reduced pressure. The resulting residue is purified by flash chromatography (silica gel) with 10-15% EtOAc to give the title compound as an off-white solid (0.45 g, 27.67%). Mass spectrum (m/z): 430.0 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08642768B2
出典データセットuspto-grants-2014_02
ORD IDord-2654c8363252447cad4e00376b45a8cf
出典メモuspto-grants-2014_02