4-(5-Nitro-benzooxazol-2-YL)-1,4-diaza-bicyclo[3.2.2]nonane → 4-(5-Amino-benzooxazol-2-YL)-1,4-diaza-bicyclo[3.2.2]nonane

HRID 393540Notes

Reaction equation

HRID 393540 reaction equation
[N+:1]([C:4]1[CH:5]=[CH:6][C:7]2[O:11][C:10]([N:12]3[CH:18]4[CH2:19][CH2:20][N:15]([CH2:16][CH2:17]4)[CH2:14][CH2:13]3)=[N:9][C:8]=2[CH:21]=1)([O-])=O.[H][H]>[Pd].C(O)C>[NH2:1][C:4]1[CH:5]=[CH:6][C:7]2[O:11][C:10]([N:12]3[CH:18]4[CH2:17][CH2:16][N:15]([CH2:20][CH2:19]4)[CH2:14][CH2:13]3)=[N:9][C:8]=2[CH:21]=1

Participants

5

Reactant 2

HCID 224958014-(5-Nitro-benzooxazol-2-YL)-1,4-diaza-bicyclo[3.2.2]nonaneHCID 178418361HCID 178418361, compound

Product 1

HCID 155158954-(5-Amino-benzooxazol-2-YL)-1,4-diaza-bicyclo[3.2.2]nonaneYield 80.9%

Reagents, catalysts & solvents 2

HCID 23938PalladiumCatalystHCID 702EthanolSolvent2×

Procedure

10% Palladium on carbon (300 mg) was added to a solution of 4-(5-nitro-benzooxazol-2-yl)-1,4-diaza-bicyclo[3.2.2]nonane (288 mg, 1 mmol, prepared as in Example 21) in ethanol (5 mL) and subjected to hydrogen gas at 50 PSI at RT for a period of 16 h. The reation mixture was diluted with ethanol (20 mL) and filtered through a pad of celite. Concentration in vacuo gave 209 mg of the title compound as a brown oil: 1H NMR (CD3OD, 400 MHz) δ 7.06 (d, 1H, J=8.3 Hz), 6.75 (d, 1H, J=1.3 Hz), 6.50 (dd, 1H, J=8.3, 1.3 Hz), 4.56 (br s, 1H), 4.08 (br s, 2H), 3.62-3.47 (m, 6H), 2.34-2.31 (m, 2H), 2.20-2.16 (m, 2H); MS (Cl) m/z 259.2 (M+1).

Workup

  1. filtrationfiltered through a pad of celite
  2. concentrationConcentration in vacuo

Sources & evidence

ORD record
ord-13d97d0e36d8483c8d606e810df738b5
Source dataset
uspto-grants-2004_10
Patent number
US06809094B2

Reaction notes

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