Reaction #2122528

ord-376960eff09c45a3a5918ee005530ba5

Reaction equation

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

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  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
    OtherThe resulting crude material was submitted to a Biotage purification (350 g silica gel, CH2Cl2 elution)

Procedure

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.v1Patent: US08574563B2uspto-grants-2013_11