Aluminium lithium hydride → HCID 178463772, compound

HRID 1620132Notes

Reaction equation

HRID 1620132 reaction equation
[CH3:1][CH:2]([CH3:19])[CH:3]([NH:15][C:16](=O)[CH3:17])[C:4]1[NH:5][CH:6]=[C:7]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[N:8]=1.[H-].[H-].[H-].[H-].[Li+].[Al+3]>C1COCC1>[CH2:16]([NH:15][CH:3]([C:4]1[NH:5][CH:6]=[C:7]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[N:8]=1)[CH:2]([CH3:19])[CH3:1])[CH3:17]

Participants

4

Procedure

A solution of N-[2-methyl-1-(4-phenyl-1H-imidazol-2-yl)-propyl]-acetamide (0.077 g, 0.30 mmol) in THF (2.0 mL) was added dropwise over 10 min to a refluxing 1.0 M solution of LiAlH4 in THF (3.0 mL). The reaction was maintained at reflux for 11 h, cooled to rt, and quenched by sequential treatment with 0.11 mL of cold water (5° C.), 0.11 mL of 15% NaOH in aqueous solution, and 0.33 mL of cold water (5° C.). The resultant solid was removed by suction filtration and the filtrate (pH 8-9) was extracted three times with EtOAc. The combined organic fractions were dried over MgSO4, filtered, and concentrated to afford 0.069 g of a 5:1 mixture (determined by 1H NMR) of ethyl-[2-methyl-1-(4-phenyl-1H-imidazol-2-yl)-propyl]-amine and recovered

Workup

  1. temperatureThe reaction was maintained
  2. temperatureat reflux for 11 h
  3. customquenched by sequential treatment with 0.11 mL of cold water (5° C.), 0.11 mL of 15% NaOH in aqueous solution, and 0.33 mL of cold water (5° C.)
  4. customThe resultant solid was removed by suction filtration
  5. extractionthe filtrate (pH 8-9) was extracted three times with EtOAc
  6. dry with materialThe combined organic fractions were dried over MgSO4
  7. filtrationfiltered
  8. concentrationconcentrated

Sources & evidence

ORD record
ord-fdbfe7bc5fe24028b90ce5f6cf63f6e3
Source dataset
uspto-grants-2014_07
Patent number
US08772325B2

Reaction notes

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