تفاعل #2307965

ord-77ce91c176fb4c1ca498a4439d5ffc14

معادلة التفاعل

[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
المردود 87.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

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

الإجراء التجريبي

(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).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07368101B2uspto-grants-2008_05