Réaction #2122528

ord-376960eff09c45a3a5918ee005530ba5

Équation de réaction

COC(=O)C[C@H](N)C(=O)OCc1ccccc1
(S)-1-benzyl 4-methyl 2-aminosuccinate
BrC1(c2ccccc2)c2ccccc2-c2ccccc21
9-bromo-9-phenyl-9H-fluorene
CCN(CC)CC
Et3N
COC(=O)C[C@H](NC1(c2ccccc2)c2ccccc2-c2ccccc21)C(=O)OCc1ccccc1
(S)-1-benzyl 4-methyl 2-(9-phenyl-9H-fluoren-9-ylamino)succinate

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    FiltrationThe mixture was filtered
  2. 2
    workup.ADDITIONthe filtrate was treated with MgSO4
  3. 3
    Filtrationfiltered again
  4. 4
    Concentrationthe final filtrate was concentrated
  5. 5
    AutreThe resulting crude material was submitted to a Biotage purification (350 g silica gel, CH2Cl2 elution)

Mode opératoire

Pb(NO3)2 (6.06 g, 18.3 mmol) was added over 1 min to a CH2Cl2 (80 mL) solution of (S)-1-benzyl 4-methyl 2-aminosuccinate (4.50 g, 19.0 mmol), 9-bromo-9-phenyl-9H-fluorene (6.44 g, 20.0 mmol) and Et3N (3.0 mL, 21.5 mmol), and the heterogeneous mixture was stirred at ambient condition for 48 hr. The mixture was filtered and the filtrate was treated with MgSO4 and filtered again, and the final filtrate was concentrated. The resulting crude material was submitted to a Biotage purification (350 g silica gel, CH2Cl2 elution) to afford (S)-1-benzyl 4-methyl 2-(9-phenyl-9H-fluoren-9-ylamino)succinate as highly viscous colorless oil (7.93 g). 1H NMR (DMSO-d6, δ=2.5 ppm, 400 MHz): δ 7.82 (m, 2H), 7.39-7.13 (m, 16H), 4.71 (d, J=12.4, 1H), 4.51 (d, J=12.6, 1H), 3.78 (d, J=9.1, NH), 3.50 (s, 3H), 2.99 (m, 1H), 2.50-2.41 (m, 2H, partially overlapped with solvent). LC (Cond. 1): RT=2.16 min; LC/MS: Anal. Calcd. for [M+H]+ C31H28NO4: 478.20; found 478.19.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08574563B2uspto-grants-2013_11