Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethanolamine | HCID 700 | — |
| Edukt | Nicotinate | HCID 937 | — |
| Edukt | N-Hydroxysuccinimide | HCID 80170 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | N-succinimidyl-nicotinate | HCID 86742329 | — |
| Edukt | ethylamine DMF | HCID 86742330 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | N-(2-hydroxyethyl)nicotinamide | HCID 72663 | — |
Reaktionsschritte
The N-succinimidyl-nicotinate compound described in Example 1 was reacted with the hydrochloric salt of ethanolamine, available commercially in its radioactive form. The ethanolamine salt was dissolved in dried DMF and chilled in an ice bath. To the mixture was added an equimolar of diisopropylethylamine (DIEA) and stirred for 15 minutes. An equimolar solution of N-succinimidyl-nicotinate was added to the ethylamine-DMF mixture dropwise under a nitrogen atmosphere. As the nicotinate was added the mixture turned milky and was slurried for at least another half hour. The milky substance was the N-hydroxy-succinimide precipitating, which was filtered off. The DMF-mixture was washed with ether to remove any precipitant. The solvent mixture was removed under high vaccum. The oily mixture was triturated with ether to yield a precipitant, N-(2-hydroxyethyl)nicotinamide. The radioactive compound was isolated and identified by its TLC.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04764462 |
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| Quelldatensatz | uspto-grants-1988_08 |
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| ORD ID | ord-b5b09e4205d74d908c6d4d8044e0f888 |
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| Quellennotiz | uspto-grants-1988_08 |
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