Imidazole → 1-Acetyl-2-[1-imidazolylmethyl]-3-methylindole-5-carboxylic acid ethyl ester

HRID 2413255Notes

Reaction equation

HRID 2413255 reaction equation
[CH2:1]([O:3][C:4]([C:6]1[CH:7]=[C:8]2[C:12](=[CH:13][CH:14]=1)[N:11]([C:15](=[O:17])[CH3:16])[C:10]([CH2:18]Br)=[C:9]2[CH3:20])=[O:5])[CH3:2].[NH:21]1[CH:25]=[CH:24][N:23]=[CH:22]1.C(=O)(O)[O-].[Na+]>CC(C)=O>[CH2:1]([O:3][C:4]([C:6]1[CH:7]=[C:8]2[C:12](=[CH:13][CH:14]=1)[N:11]([C:15](=[O:17])[CH3:16])[C:10]([CH2:18][C:22]1[NH:21][CH:25]=[CH:24][N:23]=1)=[C:9]2[CH3:20])=[O:5])[CH3:2]

Participants

5

Procedure

A mixture of 1-acetyl-2-bromomethyl-3-methylindole-5-carboxylic acid ethyl ester (5.74 g), imidazole (11.56 g), sodium bicarbonate (2.9 g) and acetone was stirred for 18 hours and then evaporated. The residue was partitioned between water and ethyl acetate. The ethyl acetate layer was separated, washed with water and dried (Na2SO4). The solvent was evaporated and the residue was chromatograhed on silica gel. Elution with chloroform first gave some impurity followed by pure product. Evaporation of the product-containing fractions gave 1-acetyl-2-[1-imidazolylmethyl]-3-methylindole-5-carboxylic acid ethyl ester (4.80 g) which was used without further characterisation.

Workup

  1. customevaporated
  2. customThe residue was partitioned between water and ethyl acetate
  3. customThe ethyl acetate layer was separated
  4. washwashed with water
  5. dry with materialdried (Na2SO4)
  6. customThe solvent was evaporated
  7. washElution with chloroform
  8. customfirst gave some impurity
  9. customEvaporation of the product-containing fractions

Sources & evidence

ORD record
ord-99ec756bce0a414c8e0f653aa5e78290
Source dataset
uspto-grants-1985_01
Patent number
US04496572

Reaction notes

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