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HRID 239936作成日:2026年10月26日

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

https://huagongshe.com/reaction/239936

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物Propylphosphonic anhydrideHCID 111923—
反応物5-Bromo-2-methylbenzoic acidHCID 346004—
反応物Benzoic acid, 4-amino-3,5-dimethyl-, methyl esterHCID 11030398—
溶媒DichloromethaneHCID 6344—
生成物Methyl 4-[(5-bromo-2-methyl-benzoyl)amino]-3,5-dimethyl-benzoateHCID 86707323107.9%

反応手順

To a solution of 5-bromo-2-methylbenzoic acid (2.0 g, 0.008 mol) in CH2Cl2 (20 mL) at 0° C. are added methyl 4-amino-3,5-dimethylbenzoate (1.28 g, 0.0072, see preparation 12) and N,N-diisopropylethylamine (4.12 g, 0.032 mol). After stirring the reaction mixture for 10 minutes, 1-propanephosphonic acid cyclic anhydride (50% solution in ethyl acetate, 7.63 g, 0.024 mol) is added via syringe and stirred at 50° C. After 16 hours, the solvent is removed under reduced pressure and the residue is diluted with water and extracted twice with ethyl acetate. The organic layers are combined and dried over anhydrous Na2SO4, filtered, and concentrated under reduced pressure. The resulting residue is purified by flash chromatography (silica gel) using 12% ethyl acetate in hexane to give the title compound as a white solid (2.9 g, 97%). Mass spectrum (m/z): 376.0 (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-5df3b57330d74beebb2026f05a5b940b
出典メモuspto-grants-2014_02