Water → HCID 86672708, compound

HRID 2369907Notes

Reaction equation

HRID 2369907 reaction equation
C[O:2][CH:3](OC)[CH2:4][N:5]1[C:9]2[C:10]([C:14]([O:16][CH3:17])=[O:15])=[CH:11][CH:12]=[CH:13][C:8]=2[N:7]=[C:6]1[CH:18](C)C.O.FC(F)(F)C(O)=O>C(Cl)Cl>[CH3:18][C:6]1[N:5]([CH2:4][CH:3]=[O:2])[C:9]2[C:10]([C:14]([O:16][CH3:17])=[O:15])=[CH:11][CH:12]=[CH:13][C:8]=2[N:7]=1

Participants

5

Procedure

To a stirred solution of methyl 1-(2,2-dimethoxyethyl)-2-isopropyl-1H-benzo[d]imidazole-7-carboxylate from Step A above in methylene chloride were added water and trifluoroacetic acid and the reaction was stirred at room temperature for 2 h and then heated at reflux for 3.5 h. The reaction mixture was concentrated under reduced pressure to remove the excess trifluoroacetic acid, diluted with methylene chloride, washed with saturated aqueous sodium bicarbonate, re-extracted with methylene chloride, dried (Na2SO4), filtered, and concentrated under reduced pressure to give methyl 2-methyl-1-(2-oxoethyl)-1H-benzo[d]imidazole-7-carboxylate (0.4 g, 56%): 1H NMR (500 MHz, DMSO-d6) δ 9.70 (s, 1H), 7.81 (dd, J=8.0, 1.5 Hz, 1H), 7.67 (dd, J=7.5, 1.0 Hz, 1H), 7.25 (t, J=8.0 Hz, 1H), 5.38 (s, 2H), 3.84 (s, 3H), 2.47 (s, 3H); MS (ESI+) m/z 233 (M+H).

Workup

  1. temperatureheated
  2. temperatureat reflux for 3.5 h
  3. concentrationThe reaction mixture was concentrated under reduced pressure
  4. customto remove the excess trifluoroacetic acid
  5. additiondiluted with methylene chloride
  6. washwashed with saturated aqueous sodium bicarbonate
  7. extractionre-extracted with methylene chloride
  8. dry with materialdried (Na2SO4)
  9. filtrationfiltered
  10. concentrationconcentrated under reduced pressure

Sources & evidence

ORD record
ord-887dc0f1973d4ca1a10663a5f25eb8d7
Source dataset
uspto-grants-2014_04
Patent number
US08710046B2

Reaction notes

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