반응 #2307965

ord-77ce91c176fb4c1ca498a4439d5ffc14

반응 방정식

[Na+].[OH-]
NaOH
CC(=O)O[C@@H](C)C(=O)Cl
(S)-2-(Acetyloxy)propanoyl chloride
CC(=O)OCC(COC(C)=O)NC(=O)c1c(I)c(N)c(I)c(C(=O)NC(COC(C)=O)COC(C)=O)c1I
N,N′-bis[2-acetyloxy-1-[(acetyloxy)methyl]ethyl]-5-amino-2,4,6-triiodo-1,3-benzenedicarboxamide
CC(=O)O[C@@H](C)C(=O)Cl
(S)-2-(acetyloxy)propanoyl chloride
C[C@H](O)C(=O)Nc1c(I)c(C(=O)NC(CO)CO)c(I)c(C(=O)NC(CO)CO)c1I
Iopamidol
수율 87.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타the temperature of the reaction mixture below 30° C
  2. 2
    workup.STIRRINGvigorously stirred at 45° C
  3. 3
    농축After two hours the mixture is concentrated under vacuum
  4. 4
    여과After two hours at room temperature the resulting suspension is filtered
  5. 5
    세척the solid washed with N,N-dimethylacetamide (2×20 mL)
  6. 6
    농축are concentrated to an oily residue, which
  7. 7
    workup.ADDITIONis diluted with water (200 mL)
  8. 8
    세척is eluted with water
  9. 9
    농축The eluate is concentrated and loaded onto two ion exchange resin columns (Dowex® C350 15 mL, Relite® MG1 10 mL)
  10. 10
    농축The eluate is concentrated
  11. 11
    기타the solid residue is crystallized from ethanol

실험 절차

(S)-2-(Acetyloxy)propanoyl chloride (16.5 g, 110 mmol) is added, over 20 min, to a stirred solution of N,N′-bis[2-acetyloxy-1-[(acetyloxy)methyl]ethyl]-5-amino-2,4,6-triiodo-1,3-benzenedicarboxamide (53.3 g, 61.1 mmol) in N,N-dimethylacetamide (75 mL) while keeping the temperature of the reaction mixture below 30° C. A further amount of (S)-2-(acetyloxy)propanoyl chloride (0.9 g, 6.0 mmol) is added after 24 and 30 hours and the reaction mixture is stirred at the same temperature for additional 15 hours. 5M NaOH (90 mL, 450 mmol) is dripped over a period of 2 hours into the reaction mixture vigorously stirred at 45° C. After two hours the mixture is concentrated under vacuum and reintegrated with additional N,N-dimethylacetamide (200 mL). After two hours at room temperature the resulting suspension is filtered and the solid washed with N,N-dimethylacetamide (2×20 mL). The mother liquors, combined with the washings, are concentrated to an oily residue, which is diluted with water (200 mL) and nanofiltered. The retentate is loaded onto an Amberlite® XAD-16.00 resin column (160 mL) that is eluted with water. The eluate is concentrated and loaded onto two ion exchange resin columns (Dowex® C350 15 mL, Relite® MG1 10 mL). The eluate is concentrated and the solid residue is crystallized from ethanol to afford Iopamidol (41.2 g, 53 mmol).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07368101B2uspto-grants-2008_05