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HRID 239978作成日:2026年10月26日

Diisopropylethylamine → Methyl 4-[(2-chloroquinoline-4-carbonyl)amino]-3,5-dimethyl-benzoate

https://huagongshe.com/reaction/239978

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2-Chloroquinoline-4-carboxylic acidHCID 230582—
反応物Benzoic acid, 4-amino-3,5-dimethyl-, methyl esterHCID 11030398—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物Methyl 4-[(2-chloroquinoline-4-carbonyl)amino]-3,5-dimethyl-benzoateHCID 86707363960.3%

反応条件

温度40 °C

反応手順

To a solution of 2-chloroquinoline-4-carboxylic acid (5.00 g, 0.0024 mol) in CH2Cl2 (50 mL) at 0° C. are added methyl 4-amino-3,5-dimethylbenzoate (3.88 g, 0.02167 mol, see preparation 12) and N,N-diisopropylethylamine (12.5 ml, 0.07225 mol). After stirring the reaction mixture for 10 minutes, 1-propanephosphonic acid cyclic anhydride (50% solution in ethyl acetate, 31.0 ml, 0.048 mol) is added via syringe and heated at 40° C. After 5 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) using a gradient of 0-40% ethyl acetate in hexanes. After purification the solid is triturated with 20% diethyl ether in pentane and dried to give the title compound as a white solid (8.50 g, 96%). Mass spectrum (m/z): 369.1 (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-543cff2aef534d55add2ec8d683941a5
出典メモuspto-grants-2014_02