4-Nitro-1-(oxetan-3-yl)-1H-imidazole → 1-(Oxetan-3-yl)-1H-imidazol-4-amine

HRID 1411996Notes

Reaction equation

HRID 1411996 reaction equation
[N+:1]([C:4]1[N:5]=[CH:6][N:7]([CH:9]2[CH2:12][O:11][CH2:10]2)[CH:8]=1)([O-])=O>[Pd].CO>[O:11]1[CH2:12][CH:9]([N:7]2[CH:8]=[C:4]([NH2:1])[N:5]=[CH:6]2)[CH2:10]1

Participants

4

Reactant 1

HCID 866845194-Nitro-1-(oxetan-3-yl)-1H-imidazole

Product 1

HCID 866845201-(Oxetan-3-yl)-1H-imidazol-4-amineYield 85%

Reagents, catalysts & solvents 2

HCID 23938PalladiumCatalystHCID 887MethanolSolvent

Procedure

A 25-mL single-neck round-bottomed flask was purged with nitrogen and charged with 285a (100 mg, 0.6 mmol), 10% palladium on carbon (10% wet, 10 mg) and methanol (10 mL). The flask was evacuated, charged with hydrogen gas (via balloon), and stirred for 1 h at room temperature. The hydrogen was then evacuated and nitrogen was charged to the flask. The catalyst was removed by filtration through a pad of CELITE® and the filtrate was concentrated under reduced pressure to afford 285b (70 mg, 85%). MS-ESI: [M+H]+ 140.3.

Workup

  1. customA 25-mL single-neck round-bottomed flask was purged with nitrogen
  2. customThe flask was evacuated
  3. additioncharged with hydrogen gas (via balloon)
  4. customThe hydrogen was then evacuated
  5. additionnitrogen was charged to the flask
  6. customThe catalyst was removed by filtration through a pad of CELITE®
  7. concentrationthe filtrate was concentrated under reduced pressure

Sources & evidence

ORD record
ord-1f3aa530f2dd4b37a1d33a3c25f1ef2b
Source dataset
uspto-grants-2014_12
Patent number
US08921353B2

Reaction notes

Loading…