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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1372744Erstellt: 25. Oktober 2026

Dimethylformamide → Methyl (3-chloro-4-((1-methyl-3-indazolylcarbonyl)amino)phenyl)acetate

https://huagongshe.com/reaction/1372744

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktTriethylamineHCID 8471—
EduktOxalyl chlorideHCID 65578—
Edukt1H-Indazole-3-carboxylic acid, 1-methyl-HCID 689105—
EduktMethyl 2-(4-amino-3-chlorophenyl)acetateHCID 13616273—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
ProduktMethyl (3-chloro-4-((1-methyl-3-indazolylcarbonyl)amino)phenyl)acetateHCID 5877839389%

Reaktionsschritte

To 1-methylindazole-3-carboxylic acid (600 mg, 3.41 mmol) and DMF (27.0 μl, 0.34 mmol) was added methylene chloride (20 ml). Under stirring at room temperature, oxalyl chloride (0.36 ml, 4.09 mmol) was added dropwise to the resulting mixture. After completion of the dropwise addition, the reaction mixture was stirred at room temperature for 50 hours and the solvent was distilled off under reduced pressure. The residue was dissolved in methylene chloride (5 ml). The resulting solution was added to a solution of methyl 4-amino-3-chlorophenylacetate (680 mg, 3.41 mmol) and triethylamine (1.42 ml, 10.2 mmol) in methylene chloride (5 ml) under stirring at room temperature. The reaction mixture was heated under reflux at room temperature for 7 hours. After the reaction mixture was cooled to room temperature, water was added thereto, followed by extraction with chloroform. The extract was washed with saturated brine, dried over anhydrous sodium sulfate, and distilled under reduced pressure to remove the solvent. The residue was purified by chromatography on a silica gel column, whereby from n-hexane-ethyl acetate (2:1, v/v) eluate fractions, methyl (3-chloro-4-((1-methyl-3-indazolylcarbonyl)amino)phenyl)acetate (1.08 g, 89%) was obtained as a yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07157487B2
Quelldatensatzuspto-grants-2007_01
ORD IDord-e74ccd3037b044969bfe2b00997d3b10
Quellennotizuspto-grants-2007_01