Water → 1-[N-(2-nitrophenyl)-2-aminoethyl]-4-(2-methoxyphenyl)piperazine

HRID 2184828Notes

Reaction equation

HRID 2184828 reaction equation
Cl[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[N+:8]([O-:10])=[O:9].[NH2:11][CH2:12][CH2:13][N:14]1[CH2:19][CH2:18][N:17]([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][C:21]=2[O:26][CH3:27])[CH2:16][CH2:15]1.C(=O)([O-])[O-].[K+].[K+].O>C(O)CCC>[N+:8]([C:3]1[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=1[NH:11][CH2:12][CH2:13][N:14]1[CH2:15][CH2:16][N:17]([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][C:21]=2[O:26][CH3:27])[CH2:18][CH2:19]1)([O-:10])=[O:9]

Participants

6

Procedure

A mixture of 3.03 g of 2-chloronitrobenzene, 4.52 g of 1-(2-aminoethyl)-4-(2-methoxyphenyl)piperazine, and 3.18 g of anhydrous potassium carbonate in 30 mL of n-butanol was stirred for 32 h at reflux. After cooling, the mixture was poured into H2O, then extracted with EtOAc and the organic phase dried on Na2SO4. The crude obtained by evaporating the solvent was purified by flash chromatography (EtOAc-petrolium ether 4:6) and the residue obtained after evaporation of the solvents was taken up with Et2O, stirred and filtered giving 2.2 g (31%) of the title compound. Melting point: 117-118° C.

Workup

  1. temperatureat reflux
  2. temperatureAfter cooling
  3. extractionextracted with EtOAc
  4. customthe organic phase dried on Na2SO4
  5. customThe crude obtained
  6. customby evaporating the solvent
  7. customwas purified by flash chromatography (EtOAc-petrolium ether 4:6)
  8. customthe residue obtained
  9. customafter evaporation of the solvents
  10. stirringstirred
  11. filtrationfiltered

Sources & evidence

ORD record
ord-6bd0613ea79d46e285a7430682881493
Source dataset
uspto-grants-2002_06
Patent number
US06399614B1

Reaction notes

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