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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1160160Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/1160160

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHOAtHCID 181649—
Edukt1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Edukt2-Methyl-6-(trifluoromethyl)nicotinic acidHCID 2775683—
EduktMethyl 5-Amino-2-chlorobenzoateHCID 5200412—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-Chloro-5-[(2-methyl-6-trifluoromethyl-pyridine-3-carbonyl)-amino]-benzoic acid methyl esterHCID 3230793194%

Reaktionsschritte

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%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07816369B2
Quelldatensatzuspto-grants-2010_10
ORD IDord-cc6abcabe9744b53a82442c649187893
Quellennotizuspto-grants-2010_10