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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 728675Erstellt: 23. Oktober 2026

Acrylamide → 1-(2-carbamoylethyl)-5-(N-cyclopentylmethylcarbamoyl)indole

https://huagongshe.com/de/reaction/728675

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcrylamideHCID 6579—
EduktSodium hydrideHCID 24758—
EduktAmmonium ChlorideHCID 25517—
Edukt1h-Indole-5-carboxamide,n-(cyclopentylmethyl)-HCID 10037396—
LösungsmittelDimethylformamideHCID 6228—
Produkt1-(2-carbamoylethyl)-5-(N-cyclopentylmethylcarbamoyl)indoleHCID 1982247736,1%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

A solution of 5-(N-cyclopentylmethylcarbamoyl)indole (A)(1.50 g) in N,N-dimethylformamide (DMF) (5 ml) was added to a stirred slurry of sodium hydride (0.16 g) in DMF (15 ml) maintained at 0° C. under an atmosphere of nitrogen. The mixture was warmed to room temperature for 15 minutes, treated with a solution of acrylamide (0.66 g) in DMF (5 ml), and allowed to stir for 12 hours. The mixture was poured into a cold, saturated aqueous solution of ammonium chloride to give a milky suspension which was extracted with ethyl acetate. The organic phase was washed successively with water and brine, dried (MgSO4), and evaporated. The resulting clear oil was purified by flash chromatography on silica gel (700 ml), eluting with 7:93 v/v methanol:ethyl acetate, to give 1-(2-carbamoylethyl)-5-(N-cyclopentylmethylcarbamoyl)indole (0.70 g, 36%) as a gummy white foam; NMR (80 MHz, CDCl3): 1.2-2.2(broad m, 9H, cyclopentyl), 2.7(t, 2H, CH2CO), 3.4 (dd, 2H, CH2NH), 4.5(t, 2H, CH2CH2CO), 5.4(broad, 2H, CONH2), 6.5(dd, 1H, H3 -indole), 7.2(d, 1H, H2 -indole), 7.3(d, 1H, H7 -indole), 7.6(dd, 1H, H6 -indole), 8.0(m, 1H, H4 -indole).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05049679
Quelldatensatzuspto-grants-1991_09
ORD IDord-8b05121848f94a8bba8f79c029c9c427
Quellennotizuspto-grants-1991_09