Reaktion #59687

ord-42cdd1f4f85041759000fb71106a03b8

Reaktionsgleichung

O=C(O)c1ccc(I)cc1
4-Iodobenzoic acid
CN(C)C=O
dimethylformamide
CC(C)(C)OC(=O)NN
tert-butyl carbazate
CN(C)C(On1nnc2cccnc21)=[N+](C)C.F[P-](F)(F)(F)(F)F
HATU
On1nnc2ccccc21
1-hydroxybenzotriazole
CCN(C(C)C)C(C)C
N,N-diisopropylethylamine
CC(C)(C)C(=O)NNC(=O)c1ccc(I)cc1
desired product
CC(C)(C)C(=O)NNC(=O)c1ccc(I)cc1
4Iodo-benzoic acid N′-(2,2-dimethyl-propionyl)-hydrazide

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe solvent was removed in vacuo
  2. 2
    Sonstigethe residue partitioned between dichloromethane (75 ml) and saturated aqueous sodium bicarbonate solution (75 ml)
  3. 3
    WaschenThe organic layer was washed with water (100 ml), brine (100 ml)
  4. 4
    Trocknendried over magnesium sulfate
  5. 5
    Filtrationfiltered
  6. 6
    Sonstigethe solvent removed in vacuo

Vorschrift

4-Iodobenzoic acid (5 g, 20.2 mmol) was dissolved in dimethylformamide (50 ml). To this was added tert-butyl carbazate (2.66 g, 20.2 mmol), HATU (9.2 g, 24.2 mmol), 1-hydroxybenzotriazole (2.7 g, 20.2 mmol) and N,N-diisopropylethylamine (10.5 ml, 60.5 mmol). The mixture was stirred for 17 hours at room temperature. The solvent was removed in vacuo and the residue partitioned between dichloromethane (75 ml) and saturated aqueous sodium bicarbonate solution (75 ml). The organic layer was washed with water (100 ml), brine (100 ml), dried over magnesium sulfate, filtered and the solvent removed in vacuo. The desired product was obtained as a cream solid (4.6 g, 12.7 mmol).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07425555B2uspto-grants-2008_09