Ethyl Acetate → HCID 178440076, Verbindung

HRID 53038Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 53038
C(N(CC)C(C)C)(C)C.[OH:10][C:11]([C:14]1[N:15]=[C:16]([CH2:22][CH2:23][CH3:24])[NH:17][C:18]=1[C:19]([OH:21])=[O:20])([CH3:13])[CH3:12].[CH3:25][C:26]1[O:30][C:29](=[O:31])[O:28][C:27]=1[CH2:32]Cl.C(OCC)(=O)C>CN(C)C(=O)C.O>[OH:10][C:11]([C:14]1[N:15]=[C:16]([CH2:22][CH2:23][CH3:24])[NH:17][C:18]=1[C:19]([O:21][CH2:32][C:27]1[O:28][C:29](=[O:31])[O:30][C:26]=1[CH3:25])=[O:20])([CH3:13])[CH3:12]

Komponenten

7

Versuchsvorschrift

1.76 ml of N,N-diisopropylethylamine were added to a suspension of 1.06 g of 4-(1-hydroxy-1-methylethyl)-2-propylimidazole-5-carboxylic acid [prepared as described in Preparation 22(i)] in 10 ml of N,N-dimethylacetamide, and the resulting mixture was stirred at room temperature for 10 minutes, after which 1.12 g of (5-methyl-2-oxo-1,3-dioxolen-4-yl)methyl chloride was added, and the mixture was stirred at 60° C. for 4 hours. At the end of this time, the reaction mixture was mixed with ethyl acetate and water. The ethyl acetate layer was separated and concentrated by evaporation under reduced pressure, and the concentrate was purified by column chromatography through silica gel, using a 1:15 by volume mixture of methanol and methylene chloride as the eluent, to give 1.14 g of the title compound as a viscous oil.

Aufarbeitung

  1. stirringthe mixture was stirred at 60° C. for 4 hours
  2. customThe ethyl acetate layer was separated
  3. concentrationconcentrated by evaporation under reduced pressure
  4. customthe concentrate was purified by column chromatography through silica gel
  5. additionby volume mixture of methanol and methylene chloride as the eluent

Quellen und Nachweise

ORD-Eintrag
ord-77263688991d49449e335cb5d66ac1fd
Quelldatensatz
uspto-grants-1997_04
Patentnummer
US05616599

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