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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1828280Erstellt: 25. Oktober 2026

5-Fluoroindole-2-carboxylic acid → 5-fluoro-2-{[4-(2-pyridinyl)-1-piperazinyl]carbonyl}-1H-indole

https://huagongshe.com/reaction/1828280

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt5-Fluoroindole-2-carboxylic acidHCID 1820—
Edukt1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Edukt1-(2-Pyridyl)piperazineHCID 94459—
LösungsmittelDichloromethaneHCID 6344—
Produkt5-fluoro-2-{[4-(2-pyridinyl)-1-piperazinyl]carbonyl}-1H-indoleHCID 22065982—

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

5-Fluoro-1H-indole-2-carboxylic acid (4.0 g) and EDCI (4.29 g) were combined in dichloromethane (90 mL) and treated with 1-(2-pyridinyl)piperazine (3.64 g). After stirring at 25° C. for 24 hours, the mixture was washed with 150 mL of water and filtered. The filter cake was washed in succession with 300 mL of water, 250 mL of dichloromethane and 20 mL of ethyl acetate to provide the title compound. 1H NMR (d6-DMSO, 300 MHz) δ 3.61 (m, 4H), 3.85 (m, 4H), 6.67 (dd, 1H, J=7.5, 4.8 Hz), 6.85 (m, 2H), 7.06 (m, 1H), 7.40 (m, 2H), 7.65 (m, 1H), 8.04 (dd, 1H, J=4.5, 1.8 Hz), 11.72 (bs, 1H). MS (DCI/NH3) m/z 325 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07057042B2
Quelldatensatzuspto-grants-2006_06
ORD IDord-a44d2f7e66fb4833ab5fe2e067712ffc
Quellennotizuspto-grants-2006_06