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HRID 1160160作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/1160160

反応式

関与物質

役割名称HCID仕込み量
反応物HOAtHCID 181649—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物2-Methyl-6-(trifluoromethyl)nicotinic acidHCID 2775683—
反応物Methyl 5-Amino-2-chlorobenzoateHCID 5200412—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物2-Chloro-5-[(2-methyl-6-trifluoromethyl-pyridine-3-carbonyl)-amino]-benzoic acid methyl esterHCID 3230793194%

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07816369B2
出典データセットuspto-grants-2010_10
ORD IDord-cc6abcabe9744b53a82442c649187893
出典メモuspto-grants-2010_10