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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1826998Erstellt: 25. Oktober 2026

Methanol → 3-[1-(3,5-Dimethyl-1h-pyrrol-2-yl)-meth-(z)-ylidene]-2-oxo-2,3-dihydro-indole-1-carboxylic acid methyl ester

https://huagongshe.com/reaction/1826998

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
Edukt3-[1-(3,5-Dimethyl-1h-pyrrol-2-yl)-meth-(z)-ylidene]-1-(imidazol-1-ylcarbonyl)-1,3-dihydro-indol-2-oneHCID 60111231—
Produkt3-[1-(3,5-Dimethyl-1h-pyrrol-2-yl)-meth-(z)-ylidene]-2-oxo-2,3-dihydro-indole-1-carboxylic acid methyl esterHCID 6011122363%

Reaktionsschritte

A reaction mixture of 3-[1-(3,5-dimethyl-1H-pyrrol-2-yl)-meth-(Z)-ylidene]-1-(imidazole-1-ylcarbonyl)-1,3-dihydro-indol-2-one (5.3 mg, 0.016 mmol) in 1.0 mL of methanol was stirred at room temperature for 64 h and filtered. The red solid was washed with methanol and dried in a vacuum oven overnight to afford 3-[1-(3,5-dimethyl-1H-pyrrol-2-yl)-meth-(Z)-ylidene]-2-oxo-2,3-dihydro-indole-1-carboxylic acid methyl ester (3.0 mg, 63%) as a red solid. 1H NMR (400 MHz, DMSO-d6) d 12.63 (s, 1H, NH-1′), 7.84–7.86 (m, 1H), 7.69 (s, 1H, H-vinyl), 7.56–7.68 (m, 1H), 7.19–7.22 (m, 2H), 6.06 (d, J=2.34 Hz, 1H, H-4′), 4.08 (s, 3H, OCH3), 2.40 (s, 3H, CH3), and 2.36 (s, 3H, CH3). MS m/z (relative intensity, %) 297 (100, [M+1]+.)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07053114B2
Quelldatensatzuspto-grants-2006_05
ORD IDord-96b74cd844cf469784a0f4137eea7ccc
Quellennotizuspto-grants-2006_05