Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Pyridine | HCID 1049 | — |
| Edukt | Acetic Anhydride | HCID 7918 | — |
| Edukt | Dimethylacetamide | HCID 31374 | — |
| Edukt | 3-[(2-Hydroxyethyl)amino]propane-1,2-diol | HCID 15034945 | — |
| Lösungsmittel | Sodium Carbonate | HCID 10340 | — |
| Produkt | 3,5-Dioxohexanoic acid | HCID 5459844 | — |
Reaktionsschritte
As in Example 12, the title compound is prepared stepwise by first reacting 5-amino-2,4,6-triiodo-3-N-methylaminocarbonylbenzoyl chloride with 3-(N-2-hydroxyethyl)amino-1, 2-propanediol dissolved in DMAc in the presence of sodium carbonate. The product, 5-amino[N-(2,3,-dihydroxypropyl)-N-(2-hydroxyethyl]-2,4,6-triiodo-3-N-methylaminocarbonylbenzamide, is reacted with acetic anhydride in the presence of pyridine to produce the triacetate, [N-(2-acetoxyethyl)-N-(2,3-diacetoxypropyl)]-5-amino-,4,6-triiodo -3-N-methylaminocarbonylbenzamide. This compound is then reacted with 2,4-dibromobutryl bromide, prepared as in Example 12, Step B, and the product is then cyclized, hydrolyzed, and purified as in Example 12, Steps D and E to produce the final product.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05075502 |
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| Quelldatensatz | uspto-grants-1991_12 |
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| ORD ID | ord-fc367aa39780419a8b3544359115cef5 |
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| Quellennotiz | uspto-grants-1991_12 |
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