Ethyl Acetate → N,4-dimethyl-1H-benzo[d]imidazole-2-carboxamide

HRID 1533749

Reaktionsgleichung

Reaktionsgleichung von HRID 1533749
[NH2:1][C:2]1[C:7]([NH2:8])=[CH:6][CH:5]=[CH:4][C:3]=1[CH3:9].[CH3:10][NH:11][C:12](=[O:18])[C:13](OCC)=O.C(=O)(O)[O-].[Na+].C(OCC)(=O)C>CN(C)C=O>[CH3:9][C:3]1[C:2]2[N:1]=[C:13]([C:12](=[O:18])[NH:11][CH3:10])[NH:8][C:7]=2[CH:6]=[CH:5][CH:4]=1

Komponenten

6

Edukt 4

HCID 8857Ethyl AcetateHCID 175932,3-DiaminotolueneHCID 516892Sodium BicarbonateHCID 3413434Ethyl 2-(methylamino)-2-oxoacetate

Produkt 1

HCID 18355052N,4-dimethyl-1H-benzo[d]imidazole-2-carboxamideAusbeute 37,8 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Reaktionsbedingungen

Temperatur
175 °C

Versuchsvorschrift

A mixture of 2,3-diaminotoluene (2.0 g) and ethyl N-methyloxamate (2.36 g) in N,N-dimethylformamide (10 ml) was stirred at 175° C. for 8 hours. After being cooled to ambient temperature, the mixture was poured into a mixture of saturated aqueous sodium bicarbonate solution and ethyl acetate and the organic layer was separated. The organic layer was washed with brine and the solution was dried over magnesium sulfate. The solvent was evaporated in vacuo and the residue was chromatographed on silica gel eluting with a mixture of chloroform and methanol (50:1) to give 4-methyl-2-(N-methylcarbamoyl)-1 H-benzimidazole (1.17 g) as a powder.

Aufarbeitung

  1. temperatureAfter being cooled to ambient temperature
  2. customthe organic layer was separated
  3. washThe organic layer was washed with brine
  4. dry with materialthe solution was dried over magnesium sulfate
  5. customThe solvent was evaporated in vacuo
  6. customthe residue was chromatographed on silica gel eluting with a mixture of chloroform and methanol (50:1)

Quellen und Nachweise

ORD-Eintrag
ord-f9f8202b6033482b994e750c0abba420
Quelldatensatz
uspto-grants-2001_03
Patentnummer
US06207693B1

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