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HRID 239982作成日:2026年10月26日

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

https://huagongshe.com/reaction/239982

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2-Chloroquinoline-4-carboxylic acidHCID 230582—
反応物Methyl 3-amino-2,4-dimethylbenzoateHCID 66871802—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物Methyl 3-[(2-chloroquinoline-4-carbonyl)amino]-2,4-dimethyl-benzoateHCID 8670736787.7%

反応手順

To a solution of 2-chloroquinoline-4-carboxylic acid (0.40 g, 0.0019 mol) in CH2Cl2 (8 mL) at 0° C. are added methyl 3-amino-2,4-dimethylbenzoate (0.31 g, 0.0017 mol, see preparation 10) and triethylamine (0.80 ml, 0.0058 mol). After stirring the reaction mixture for 10 minutes, 1-propanephosphonic acid cyclic anhydride (50% solution in ethyl acetate, 2.45 ml, 0.0038 mol) is added via syringe and stirred at room temperature. After 16 hours, the reaction is diluted with water and extracted twice with dichloromethane. The organic layers are combined and dried over magnesium sulfate, filtered, and concentrated under reduced pressure. The resulting residue is triturated with 20% diethyl ether in pentane and filtered to give the title compound as an off-white solid (0.55 g, 77%). 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-6f0ea8d061d54ba3b40e3ef34ccef83c
出典メモuspto-grants-2014_02