Reaktion #1453461

ord-04d030a48b7e48d19fdfdf13df8cb3b4

Reaktionsgleichung

Cc1ccc(C(=O)O)cc1[N+](=O)[O-]
4-methyl-3-nitro-benzoic acid
CCCCOC(=O)N1CCNCC1
N-butoxycarbonyl-piperazine
CCN(CC)CC
triethylamine
CN(C)C(On1nnc2ccccc21)=[N+](C)C.F[B-](F)(F)F
TBTU
On1nnc2cccnc21
HOAt
Cc1ccc(C(=O)N2CCN(C(=O)OC(C)(C)C)CC2)cc1[N+](=O)[O-]
4-(4-methyl-3-nitrobenzoyl)-piperazine-1-carboxylic acid tert-butyl ester

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Extraktionextracted twice with ethyl acetate
  2. 2
    WaschenThe organic layer is washed with water
  3. 3
    Trocknenbrine, dried over magnesium sulfate
  4. 4
    Sonstigeevaporated in vacuo
  5. 5
    SonstigeThe residue is purified with silica gel column chromatography (n-hexane:ethyl acetate=5:1)

Vorschrift

To a solution of 4-methyl-3-nitro-benzoic acid (300 mg, 2.76 mmol), N-butoxycarbonyl-piperazine (340 mg, 1.83 mmol) in DMF (3.0 mL), triethylamine (300 μL, 3.59 mmol), TBTU (800 mg, 2.49 mmol) and HOAt (270.5 mg, 1.99 mmol) are added and stirred at room temperature for 24 hours. The mixture is poured into water and extracted twice with ethyl acetate. The organic layer is washed with water and then brine, dried over magnesium sulfate, and evaporated in vacuo. The residue is purified with silica gel column chromatography (n-hexane:ethyl acetate=5:1) to afford 4-(4-methyl-3-nitrobenzoyl)-piperazine-1-carboxylic acid tert-butyl ester as a colorless solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07893074B2uspto-grants-2011_02