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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1160160생성일: 2026년 10월 25일

HOAt → 2-Chloro-5-[(2-methyl-6-trifluoromethyl-pyridine-3-carbonyl)-amino]-benzoic acid methyl ester

https://huagongshe.com/reaction/1160160

반응식

참여 물질

역할이름HCID투입량
반응물HOAtHCID 181649—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물2-Methyl-6-(trifluoromethyl)nicotinic acidHCID 2775683—
반응물Methyl 5-Amino-2-chlorobenzoateHCID 5200412—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물2-Chloro-5-[(2-methyl-6-trifluoromethyl-pyridine-3-carbonyl)-amino]-benzoic acid methyl esterHCID 3230793194%

반응 단계

To a solution of 2-methyl-6-trifluoromethylnicotinic acid (4.77 g; 23 mmol) in dimethyl formamide (100 ml) was added 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (4.46 g; 23 mmol) and 1-hydroxy-7-azabenzotriazole (3.17 g; 23 mmol) and the resulting solution was stirred at room temperature for 30 minutes. To this was added a solution of methyl 5-amino-2-chlorobenzoate (3.6 g; 19 mmol) in dimethyl formamide (25 ml) and the resulting solution stirred at room temperature for 18 hours. Water (200 ml) was added to the reaction mixture and this was extracted with ethyl acetate (3×200 ml). The combined organic layers were washed with saturated sodium bicarbonate solution (2×300 ml). The organic layer was dried (magnesium sulphate), filtered and evaporated to give 2-chloro-5-[(2-methyl-6-trifluoromethyl-pyridine-3-carbonyl)-amino]-benzoic acid methyl ester (6.6 g, 94%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07816369B2
출처 데이터셋uspto-grants-2010_10
ORD IDord-cc6abcabe9744b53a82442c649187893
출처 메모uspto-grants-2010_10