反应 #710510

ord-a3ee4e4b29b1461dba69cb5627613f35

反应方程式

CN1CCOCC1
N-methyl morpholine
CC1(C)S[C@@H]2[C@H](NC(=O)[C@H](N)c3ccccc3)C(=O)N2[C@H]1C(=O)O.O.O.O
ampicillin trihydrate
CCN(CC)CC
Et3N
CC(C)COC(=O)Cl
isobutyl chloroformate
CC1(C)S[C@@H]2[C@H](NC(=O)[C@H](N)c3ccccc3)C(=O)N2[C@H]1C(=O)O
10
收率 180.5%
CC1(C)S[C@@H]2[C@H](NC(=O)[C@H](N)c3ccccc3)C(=O)N2[C@H]1C(=O)O
Ampicillin
收率 180.5%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.STIRRINGthe mixture was stirred for 1 h at 0° C. and 1 h at room temperature
  2. 2
    其他After removal of the THF under vacuum
  3. 3
    workup.DISSOLUTIONthe residue was dissolved in 5 mL of water
  4. 4
    萃取The resulting suspension was extracted with EtOAc (5 mL×3)
  5. 5
    洗涤the combined organic layers were washed with brine
  6. 6
    干燥dried over Na2SO4
  7. 7
    过滤filtered
  8. 8
    其他The solvent was removed under vacuum
  9. 9
    其他the residue was purified by preparative HPLC
  10. 10
    workup.ADDITIONThe fractions containing product

实验过程

To a solution of acid 9 (22 mg, 0.023 mmol) and N-methyl morpholine (2.5 μL, 0.023 mmol) in 1 mL of anhydrous THF cooled to 0° C. was added isobutyl chloroformate (3.0 μL, 0.023 mmol) and the mixture was stirred for 1 hour at that temperature. A solution of ampicillin trihydrate (10.6 mg, 0.026 mmol) and Et3N (10 μL) in 1 mL of THF/H2O 4:1 was added and the mixture was stirred for 1 h at 0° C. and 1 h at room temperature. After removal of the THF under vacuum, the residue was dissolved in 5 mL of water and the solution was acidified to pH=2 with 1 N HCl. The resulting suspension was extracted with EtOAc (5 mL×3) and the combined organic layers were washed with brine, dried over Na2SO4 and filtered. The solvent was removed under vacuum and the residue was purified by preparative HPLC. The fractions containing product was combined and lyophilized to give conjugate 10 (16.4 mg, 55%) as a white solid: 1H NMR (600 MHz, DMSO-d6) δ9.06 (d, J=7.6 Hz, 1H), 8.54 (d, J=8.5 Hz, 1H), 8.31 (t, J=5.6 Hz, 3H), 7.40-7.44 (m, 5H), 7.24-7.36 (m, 9H), 7.12 (s, 1H), 5.71 (d, J=8.2 Hz, 1H), 5.46 (dd, J=7.9, 4.1 Hz, 1H), 5.35 (d, J=4.1 Hz, 1H), 4.11 (s, 1H), 3.12-3.16 (m, 6H), 2.43-2.45 (m, 2H), 2.30-2.34 (m, 2H), 2.27 (s, 9H), 2.20 (s, 9H), 1.59-1.65 (m, 6H), 1.53 (s, 3H), 1.37-1.43 (m, 9H); HRMS (ESI) calcd. for C63H72N7O21S (M+H)+: 1294.4496, found 1294.4522; HPLC retention time 5.57 min.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US09302012B2uspto-grants-2016_04