Dimethylacetamide → 3-(5-Isopropyl-[1,2,4]triazol-1-yl)-5-(5-methyl-pyridin-2-yl)-benzoic acid methyl ester

HRID 2092634Notes

Reaction equation

HRID 2092634 reaction equation
[C:1]([NH2:6])(=O)[CH:2]([CH3:4])[CH3:3].[CH3:7]N(C(OC)OC)C.CC(N(C)C)=O.[CH3:21][O:22][C:23](=[O:39])[C:24]1[CH:29]=[C:28]([C:30]2[CH:35]=[CH:34][C:33]([CH3:36])=[CH:32][N:31]=2)[CH:27]=[C:26]([NH:37][NH2:38])[CH:25]=1>C(O)(=O)C>[CH3:21][O:22][C:23](=[O:39])[C:24]1[CH:29]=[C:28]([C:30]2[CH:35]=[CH:34][C:33]([CH3:36])=[CH:32][N:31]=2)[CH:27]=[C:26]([N:37]2[C:1]([CH:2]([CH3:4])[CH3:3])=[N:6][CH:7]=[N:38]2)[CH:25]=1

Participants

6

Conditions

Temperature
80 °C

Procedure

Isobutyramide (6.02 g, 69 mmol) and DMFDMA (9.22 mL) were added to 10 mL of DMA in a first flask, and the mixture was heated to 80° C. with stirring for one hour. In a second flask, a suspension of 3-hydrazino-5-(5-methyl-pyridin-2-yl)-benzoic acid methyl ester (6.42 g, 23 mmol) was suspended in acetic acid and heated t 80° C. The contents of the first flask were slowly added to the second flask, and the combined mixture was stirred at 80° C. for two hours. The reaction mixture was cooled and concentrated under reduced pressure. The residue was diluted with EtOAc, washed with saturated aqueous NaHCO3 and water, dried (MgSO4), filtered and concentrated under reduced pressure. The residue was purified via flash chromatography (hexanes/EtOAc 4: - - - 2:1) to give 2.06 g of 3-(5-isopropyl-[1,2,4]triazol-1-yl)-5-(5-methyl-pyridin-2-yl)-benzoic acid methyl ester as a clear oil, MS (M+H)=337.

Workup

  1. temperatureheated t 80° C
  2. additionThe contents of the first flask were slowly added to the second flask
  3. stirringthe combined mixture was stirred at 80° C. for two hours
  4. temperatureThe reaction mixture was cooled
  5. concentrationconcentrated under reduced pressure
  6. additionThe residue was diluted with EtOAc
  7. washwashed with saturated aqueous NaHCO3 and water
  8. dry with materialdried (MgSO4)
  9. filtrationfiltered
  10. concentrationconcentrated under reduced pressure
  11. customThe residue was purified via flash chromatography (hexanes/EtOAc 4: - - - 2:1)

Sources & evidence

ORD record
ord-27a296e01e5249e092442cf06d4b8400
Source dataset
uspto-grants-2013_05
Patent number
US08440708B2

Reaction notes

Loading…