Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 18271Erstellt: 24. Oktober 2026

ethyl 4,6-dichloro-1-methyl-1H-indole-2-carboxylate → N,1-dimethylindole-2-carboxamide

https://huagongshe.com/de/reaction/18271

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktethyl 4,6-dichloro-1-methyl-1H-indole-2-carboxylateHCID 22139053—
EduktMonomethylamine methanolHCID 57454252—
ProduktN,1-dimethylindole-2-carboxamideHCID 1230331599%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

A suspension of ethyl 4,6-dichloro-1-methyl-1H-indole-2-carboxylate (1.06 g, 3.90 mmole) in 2.0 M CH3NH2/CH3OH (40 mL) in a sealed pressure bottle was heated in an oil bath preset at 50° C. A homogeneous solution formed within 2.5 hr. The reaction was kept at 50° C. for 17.5 hr, during which time a solid precipitated. The mixture was cooled to RT and poured into H2O (40 mL). The resulting mixture was concentrated on the rotavap to remove the methanol, and the solid was collected by suction filtration. This was washed with plenty of H2O and dried in high vacuum at 45-50° C. to afford the title compound (0.99 g, 99%) as an off-white solid: 1H NMR (400 MHz, CDCl3) δ 7.29 (s, 1 H), 7.16 (d, J=1.5 Hz, 1 H), 6.86 (s, 1 H), 6.21 (br s, 1 H), 4.02 (s, 3 H), 3.02 (d, J=4.9 Hz, 3 H); MS (ES) m/e 257 and 259 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07741339B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-aa345c6a0d774baf803d5bbb2876f9e1
Quellennotizuspto-grants-2010_06