2-(Hydroxymethyl)pyrrolidine-3,4-diol → 1,4-Dideoxy-1,4-imino-d-arabinitol
Reaktionsgleichung
[OH:1][CH:2]1[CH:6]([OH:7])[CH2:5][NH:4][CH:3]1[CH2:8][OH:9].[C:10]([C@H:13]([C@@H:15]([C:17]([O-:19])=[O:18])[OH:16])[OH:14])([O-:12])=[O:11].C(O[C@H]1[C@H](OCC2C=CC=CC=2)[C@@H](COCC2C=CC=CC=2)NC1)C1C=CC=CC=1>C(O)(=O)C.CO.[Pd]>[OH:1][C@H:2]1[C@H:6]([OH:7])[CH2:5][NH:4][C@@H:3]1[CH2:8][OH:9].[C:10]([C@H:13]([C@@H:15]([C:17]([O-:19])=[O:18])[OH:16])[OH:14])([O-:12])=[O:11]Komponenten
8
Edukt 3
Produkt 2
Reagenzien, Katalysatoren, Lösungsmittel 3
Versuchsvorschrift
A more direct way to synthesise 3,4-dihydroxy-2-hydroxymethylpyrrolidine, D-tartrate is by reduring 2,3,5-Tri-O-benzyl-1,4-dideoxy-1,4-imino-D-arabinitol with Pd/C in glacial acetic acid. The formed, oily (2R,3R,4R)-3,4-dihydroxy-2-hydroxymethyl-pyrrolidine,acetate is dissolved in methanol and added to a solution containing D-tartraric acid at reflux and (2R,3R,4R)-3,4-dihydroxy-2-hydroxymethylpyrrolidine, D-tartrate is formed and can be isolated by filtration. Ion exchange chromatography is thereby avoided.
Aufarbeitung
- additionadded to a solution
- additioncontaining D-tartraric acid
- temperatureat reflux
Quellen und Nachweise
- ORD-Eintrag
- ord-044689dc2fd64923adc958759ad750ed
- Quelldatensatz
- uspto-grants-2001_11
- Patentnummer
- US06316489B1
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