Methanol → HCID 15224433, compound

HRID 1006622Notes

Reaction equation

HRID 1006622 reaction equation
[CH3:1][CH:2]([CH3:21])[CH2:3][N:4]1[C:16]2[C:15]3[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=3[N:9]=[CH:8][C:7]=2[N:6]=[C:5]1[CH2:17][C:18](=[O:20])[CH3:19].[BH4-].[Na+].CO.O>C(O)C>[CH3:19][CH:18]([OH:20])[CH2:17][C:5]1[N:4]([CH2:3][CH:2]([CH3:21])[CH3:1])[C:16]2[C:15]3[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=3[N:9]=[CH:8][C:7]=2[N:6]=1

Participants

6

Reactant 4

HCID 887MethanolHCID 962WaterHCID 4311764Sodium borohydrideHCID 15224432HCID 15224432, compound

Product 1

HCID 15224433HCID 15224433, compound

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

1-[1-(2-Methylpropyl)-1H-imidazo[4,5-c]quinolin-2-yl]propan-2-one (8 g, 28.4 mmol, Example 73) was suspended in ethanol (400 mL). Sodium borohydride (1.64 g, 43.3 mmol) was added and the reaction mixture was stirred at room temperature for about 2 hours. Methanol (about 20 mL) was added and stirring was continued over night. Water was added then the solvents were removed under vacuum. The residue was partitioned between methylene chloride and water. The methylene chloride layer was separated, dried over magnesium sulfate then concentrated under vacuum to give the desired product. The structure was confirmed by nuclear magnetic resonance spectroscopy.

Workup

  1. stirringstirring
  2. waitwas continued over night
  3. customthe solvents were removed under vacuum
  4. customThe residue was partitioned between methylene chloride and water
  5. customThe methylene chloride layer was separated
  6. dry with materialdried over magnesium sulfate
  7. concentrationthen concentrated under vacuum

Sources & evidence

ORD record
ord-a7b494344deb4af58dfbb559bd9e8d02
Source dataset
uspto-grants-2004_09
Patent number
US06790961B2

Reaction notes

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