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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1372712Erstellt: 26. Oktober 2026

Dimethylformamide → HCID 58778584, Verbindung

https://huagongshe.com/reaction/1372712

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktTriethylamineHCID 8471—
EduktOxalyl chlorideHCID 65578—
EduktEthyl 4-amino-5-chloro-2-fluorophenylacetateHCID 17858807—
Edukt4-Fluoro-1-methyl-1h-indole-3-carboxylic acidHCID 18385290—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 58778584HCID 5877858452%

Reaktionsschritte

To a suspension of 4-fluoro-1-methylindole-3-carboxylic acid (700 mg, 3.62 mmol) and DMF (28.0 μl, 0.36 mmol) in methylene chloride (20 ml) was added oxalyl chloride (0.35 ml, 3.99 mmol) in portions under stirring at room temperature. After the reaction mixture was stirred at room temperature for 50 minutes, oxalyl chloride (30 μl) was added, and the mixture was stirred for further 40 minutes. To the reaction mixture, a solution of ethyl (4-amino-5-chloro-2-fluorophenyl)acetate (839 mg, 3.62 mmol) and triethylamine (1.52 ml, 10.9 mmol) in methylene chloride (5 ml) was added and the mixture was heated under reflux at room temperature for 4 hours. After cooling to room temperature, the reaction mixture was added with water, followed by extraction with chloroform. The extract was washed with brine, dried over anhydrous sodium sulfate, and distilled under reduced pressure to remove the solvent. The residue was purified by chromatography opn a silica gel column, whereby from n-hexane-ethyl acetate (2:1, v/v) eluate fractions, ethyl (5-chloro-2-fluoro-4-((4-fluoro-1-methyl-3-indolylcarbonyl)amino)phenyl)acetate (762 mg, 52%) was obtained as a yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07157487B2
Quelldatensatzuspto-grants-2007_01
ORD IDord-9ef4e488fa0941d596f58d7f864149ad
Quellennotizuspto-grants-2007_01