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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 366753Erstellt: 24. Oktober 2026

Ethyl 5-formyl-4-methyl-1h-pyrrole-3-carboxylate → (Z)-5-(5-Fluoro-4-iodo-2-oxo-1,2-dihydro-indol-3-ylidenemethyl)-4-methyl-1H-pyrrole-3-carboxylic acid ethyl ester

https://huagongshe.com/de/reaction/366753

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl 5-formyl-4-methyl-1h-pyrrole-3-carboxylateHCID 236067—
Edukt5-Fluoro-4-iodoindolin-2-oneHCID 9795601—
LösungsmittelIsopropanolHCID 3776—
LösungsmittelPiperidineHCID 8082—
Produkt(Z)-5-(5-Fluoro-4-iodo-2-oxo-1,2-dihydro-indol-3-ylidenemethyl)-4-methyl-1H-pyrrole-3-carboxylic acid ethyl esterHCID 20667774—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

A suspension of 1,3-dihydro-5-fluoro-4-iodo-2H-indol-2-one (0.5 g, 1.8 mmol) (Example 2A) and 5-formyl-4-methyl-1H-pyrrole-3-carboxylic acid ethyl ester (0.39 g, 2.17 mmol) (Example 116A above) in 1% piperidine in 2-propanol (6 mL) was heated at 80° C. for 3 h. The precipitate was collected and washed with water to give (Z)-5-(5-Fluoro-4-iodo-2-oxo-1,2-dihydro-indol-3-ylidenemethyl)-4-methyl-1H-pyrrole-3-carboxylic acid ethyl ester. (Yield 0.67 g, 85%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06130239
Quelldatensatzuspto-grants-2000_10
ORD IDord-c6ed23c93cfd469f8ec129e52c6f8016
Quellennotizuspto-grants-2000_10