Reaktionsgleichung
Cl.[OH:2][CH:3]1[O:11][C@H:10]([CH2:12][OH:13])[C@H:8]([OH:9])[C@H:6]([OH:7])[C@H:4]1[NH2:5].C(N(CC)CC)C>CN(C=O)C>[OH:2][CH:3]1[O:11][C@H:10]([CH2:12][OH:13])[C@H:8]([OH:9])[C@H:6]([OH:7])[C@H:4]1[NH2:5]Komponenten
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
In 10 ml of DMF was dissolved 0.22 g of galactosamine hydrochloride (1.04×10-3 mol). After 0.15 ml (1.04×10-3 mol) of triethylamine was added to the solution, 0.30 g (1.84×10-3 mol, value calculated from apparent molecular weight per 1 unit) was added to the mixture. The reaction was carried out at room temperature for 2 days. Then the solution containing the precipitates was dialyzed (2 days) and then freeze dried to prepare a sample (charged amounts given herein are for the sample obtained by activation of the side chain using the polymer having a side chain hydrolysis rate of 28.6% described above. For other samples, about two-fold amounts of sugar and triethylamine were used in response to the rate of activation of the side chain).
Aufarbeitung
- additionwas added to the mixture
- additionThen the solution containing the precipitates
- customwas dialyzed (2 days)
- customfreeze dried
- customto prepare a sample (
- additioncharged amounts
- customobtained by activation of the side chain
- customa side chain hydrolysis rate of 28.6%
Quellen und Nachweise
- ORD-Eintrag
- ord-489831f9d3074d59b89e707cb5479ecc
- Quelldatensatz
- uspto-grants-1992_06
- Patentnummer
- US05124437
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