Реакция #1772031

ord-3f94fb62d1b34f3089949a7bb21239d1

Уравнение реакции

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

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

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

Методика

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.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08147818B2uspto-grants-2012_04