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HRID 239960作成日:2026年10月26日

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

https://huagongshe.com/reaction/239960

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 8670730981%

反応手順

To a solution of 6-chloro-3-methyl-pyridine-2-carboxylic acid (0.70 g, 4.093 mmol, see preparation 1) in CH2Cl2 (6 mL) at 0° C. are added methyl 4-amino-3,5-dimethylbenzoate (0.74 g, 4.093 mmol, see preparation 12), and triethylamine (0.83 g, 8.187 mmol). After stirring the reaction mixture for 10 minutes, 1-propanephosphonic acid cyclic anhydride (50% solution in ethyl acetate, 2.60 g, 8.187 mmol) is added via syringe and stirred at ambient temperature. After 12 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 (1.10 g, 81%). 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-55bc217fa3934dc9b7500163da0ad06d
出典メモuspto-grants-2014_02