Ethyl levulinate → 1H-Pyrrolo(1,2-a)imidazole-2,5(3H,6H)-dione, dihydro-7a-methyl-

HRID 344741

Reaktionsgleichung

Reaktionsgleichung von HRID 344741
Cl.[NH2:2][CH2:3][C:4]([NH2:6])=[O:5].[OH-].[Na+].O=[C:10]([CH3:18])[CH2:11][CH2:12][C:13](OCC)=[O:14]>O>[O:5]=[C:4]1[CH2:3][N:2]2[C:13](=[O:14])[CH2:12][CH2:11][C:10]2([CH3:18])[NH:6]1

Komponenten

5

Edukt 3

HCID 10883Ethyl levulinateHCID 14798Sodium HydroxideHCID 2723639Glycinamide hydrochloride

Produkt 1

HCID 30795901H-Pyrrolo(1,2-a)imidazole-2,5(3H,6H)-dione, dihydro-7a-methyl-Ausbeute 21 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

To a solution of glycinamide hydrochloride (18.4 g, 0.166 mol) in water (200 ml), adjusted to pH 9.5 with 10% sodium hydroxide (about 60 ml), ethyl 4-oxopentanoate (20 g, 0.139 mol) was added. The solution was refluxed for 24 hours. After cooling the solvent was evaporated under vacuum and the residue was chromatographed over silica gel (dichloromethane-methanol 9:1) to afford 4.5 g (21%) of the title compound, m.p. 187°-189° C. NMR (CDCl3): deltaH =4.17 and 3.53 (ABq, J=16 Hz, 2H, NCH2CO), 1.5 (s, 3H, CH3). MS (E.I., 70 eV, 1.5 mA) m/z=154 (M+), 139 (M--CH3)+, 111 (M--CONH)+.

Aufarbeitung

  1. additionwas added
  2. temperatureThe solution was refluxed for 24 hours
  3. temperatureAfter cooling the solvent
  4. customwas evaporated under vacuum
  5. customthe residue was chromatographed over silica gel (dichloromethane-methanol 9:1)

Quellen und Nachweise

ORD-Eintrag
ord-6ad2ce07f5384ac7a74581258ecdfb37
Quelldatensatz
uspto-grants-1991_10
Patentnummer
US05053422

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