Reacción #1726657

ord-d83be793295d48568ed796707dbff9c2

Ecuación de reacción

CC(C)N=C=NC(C)C
DIPC
CC[C@@]1(O)C(=O)OCc2c1cc1n(c2=O)Cc2cc3ccccc3nc2-1
camptothecin
NCCCC[C@@H](C(=O)O)N(C(=O)OCc1ccccc1)C(=O)OCc1ccccc1
N,N-Bis CBZ-Lysine
NCCCC[C@H](NC(=O)OCc1ccccc1)C(=O)O
CBZ-Lys

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    LavadoThe solution was washed with 0.1 N HCl
  2. 2
    Otrodried
  3. 3
    Otroevaporated under reduced pressure
  4. 4
    Otroto yield a light yellow solid, which
  5. 5
    Otrowas recrystallized from methanol

Procedimiento

N,N-Bis CBZ-Lysine (311 mg, 0.75 mmol) was dissolved in 56 mL of anhydrous methylene chloride at room temperature. To this solution were added DIPC (0.12 mL, 0.75 mmol), DMAP (0.61 mg, 0.5 mmol) and camptothecin (0.087 g, 0.25 mmol) at 0° C. The reaction mixture was allowed to warm to room temperature and left for 16 h. The solution was washed with 0.1 N HCl, dried and evaporated under reduced pressure to yield a light yellow solid, which was recrystallized from methanol to give camptothecin-20-ester of N,N-Bis CBZ-Lys 13. Purification of 13 was satisfactory based on TLC and HPLC analysis.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08110179B2uspto-grants-2012_02