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HRID 239975作成日:2026年10月26日

Diisopropylethylamine → Methyl 4-[(6-chloro-3-methyl-pyridine-2-carbonyl)amino]-3,5-dimethyl-benzoate

https://huagongshe.com/reaction/239975

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Benzoic acid, 4-amino-3,5-dimethyl-, methyl esterHCID 11030398—
反応物6-Chloro-3-methylpyridine-2-carboxylic acidHCID 46941470—
溶媒DichloromethaneHCID 6344—
生成物Methyl 4-[(6-chloro-3-methyl-pyridine-2-carbonyl)amino]-3,5-dimethyl-benzoateHCID 8670730982.8%

反応手順

To a solution of 6-chloro-3-methyl-pyridine-2-carboxylic acid (6.00 g, 0.03508 mol) in CH2Cl2 (50 ml) at 0° C. are added methyl 4-amino-3,5-dimethylbenzoate (5.65 g, 0.03157 mol), and N,N-diisopropylethylamine (15.1 ml, 0.0877 mol). After stirring the reaction mixture for 10 minutes, 1-propanephosphonic acid cyclic anhydride (50% solution in ethyl acetate, 22.32 g, 0.07016 mol) is added via syringe and stirred at 60° C. After 3 hours, the solvent is removed under reduced pressure and the residue is diluted with water and extracted 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 a gradient of 0-40% ethyl acetate in hexanes to give the title compound as an off-white solid (8.70 g, 74%). Mass spectrum (m/z): 333.2 (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-5fa620b751ca4b1bb62e6844381bd599
出典メモuspto-grants-2014_02