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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 239960생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/239960

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Propylphosphonic anhydrideHCID 111923—
반응물Benzoic acid, 4-amino-3,5-dimethyl-, methyl esterHCID 11030398—
반응물6-Chloro-3-methylpyridine-2-carboxylic acidHCID 46941470—
용매DichloromethaneHCID 6344—
생성물Methyl 4-[(6-chloro-3-methyl-pyridine-2-carbonyl)amino]-3,5-dimethyl-benzoateHCID 8670730981%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08642768B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-55bc217fa3934dc9b7500163da0ad06d
출처 메모uspto-grants-2014_02