Sodium Bicarbonate → HCID 18429137, compound
Reaction equation
[NH2:1][C:2]1[C:3]([I:40])=[C:4]([CH2:35][O:36][C:37](=[O:39])[CH3:38])[C:5]([I:34])=[C:6]([C:32]=1[I:33])[C:7]([N:9]([CH2:21][CH:22]([O:28]C(=O)C)[CH2:23][O:24]C(=O)C)[CH2:10][CH:11]([O:17]C(=O)C)[CH2:12][O:13]C(=O)C)=[O:8].[C:41]([O:44][CH:45]([CH2:49][CH2:50][CH2:51][Cl:52])[C:46](Cl)=[O:47])(=[O:43])[CH3:42].C(=O)([O-])O.[Na+]>CN(C)C(=O)C>[C:41]([O:44][CH:45]([CH2:49][CH2:50][CH2:51][Cl:52])[C:46]([NH:1][C:2]1[C:3]([I:40])=[C:4]([CH2:35][O:36][C:37](=[O:39])[CH3:38])[C:5]([I:34])=[C:6]([C:32]=1[I:33])[C:7]([N:9]([CH2:21][CH:22]([OH:28])[CH2:23][OH:24])[CH2:10][CH:11]([OH:17])[CH2:12][OH:13])=[O:8])=[O:47])(=[O:43])[CH3:42]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
5-Amino-3-acetoxymethyl-N,N-bis-(2,3-diacetoxypropyl)-2,4,6-triiodobenzamide g, 6.85 mmol) was dissolved in dry N,N-dimethylacetamide (10 ml) and the mixture was cooled in an ice-bath. 2-Acetoxy-5-chloropentanoyl chloride (4.36g, mmol) was then added dropwise. The mixture was stirred at room temperature for 24 h, and then added slowly to aqueous sodium hydrogen carbonate (5%, 600 ml) with efficient stirring. A precepitate was formed and filtered off, redissolved in methylene chloride (250 ml) which was washed with water (6×70 ml), dried (Na2SO4) and concentrate in vacuo. The residue was chromatographed on a column of silica gel using heptane/ethyl acetate (3/7) as the eluent Yield: 7.30 g (97%).
Workup
- temperaturethe mixture was cooled in an ice-bath
- customA precepitate was formed
- filtrationfiltered off
- dissolutionredissolved in methylene chloride (250 ml) which
- washwas washed with water (6×70 ml)
- dry with materialdried (Na2SO4)
- concentrationconcentrate in vacuo
- customThe residue was chromatographed on a column of silica gel
Sources & evidence
- ORD record
- ord-5c9e5151fc1c4b7e8174567a427eb55a
- Source dataset
- uspto-grants-2001_10
- Patent number
- US06310243B1
Reaction notes
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