Acetic Acid → HCID 22402966, compound

HRID 1463201Notes

Reaction equation

HRID 1463201 reaction equation
[N+](=[CH2:3])=[N-].[CH:4]([C:7]1([CH3:27])[C:11](=[O:12])[NH:10][C:9]([C:13]2[C:21]3[N:20]=[C:19]([CH3:22])[N:18]([CH3:23])[C:17]=3[CH:16]=[CH:15][C:14]=2[C:24]([OH:26])=[O:25])=[N:8]1)([CH3:6])[CH3:5].C(O)(=O)C>CCOCC.CO>[CH:4]([C:7]1([CH3:27])[C:11](=[O:12])[NH:10][C:9]([C:13]2[C:21]3[N:20]=[C:19]([CH3:22])[N:18]([CH3:23])[C:17]=3[CH:16]=[CH:15][C:14]=2[C:24]([O:26][CH3:3])=[O:25])=[N:8]1)([CH3:6])[CH3:5]

Participants

6

Procedure

A solution of diazomethane in ether is added dropwise to a solution of the 4-(4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)-1,2-dimethyl-5-benzimidazolecarboxylic acid (2.50 g, 7.61 mmol) in methanol until the yellow color persists. The reaction mixture is neutralized with acetic acid and concentrated in vacuo. Preparative HPLC (silica gel, ethyl acetate eluent) affords the title product as off-white crystals (0.750 g, 28.9%), mp 240°-242° C.

Workup

  1. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-014c8bfbae1745189de3c08fb1bbf5fc
Source dataset
uspto-grants-1994_04
Patent number
US05300479

Reaction notes

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