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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 239982생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/239982

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Propylphosphonic anhydrideHCID 111923—
반응물2-Chloroquinoline-4-carboxylic acidHCID 230582—
반응물Methyl 3-amino-2,4-dimethylbenzoateHCID 66871802—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물Methyl 3-[(2-chloroquinoline-4-carbonyl)amino]-2,4-dimethyl-benzoateHCID 8670736787.7%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08642768B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-6f0ea8d061d54ba3b40e3ef34ccef83c
출처 메모uspto-grants-2014_02