N-Iodosuccinimide → 6-hydroxy-5-iodo-2-oxo-1H-pyridine-3-carboxamide
Reaktionsgleichung
[OH:1][C:2]1[N:10]=[C:9]([OH:11])[CH:8]=[CH:7][C:3]=1[C:4]([NH2:6])=[O:5].C1C(=O)N([I:19])C(=O)C1>C(Cl)Cl>[OH:1][C:2]1[N:10]=[C:9]([OH:11])[C:8]([I:19])=[CH:7][C:3]=1[C:4]([NH2:6])=[O:5]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of compound 2,6-dihydroxynicotinamide (20 g, 0.13 mol) and NIS (29.2 g, 0.13 mol) in DCM (1000 mL) was stirred at r.t for 20 min. The mixture was concentrated in vacuo to afford crude compound 2,6-dihydroxy-5-iodonicotinamide. (50 g) which was used for the next step directly. 1H-NMR (400 MHz, DMSO-d6) δ (ppm) 11.04 (bs, 1H), 8.46 (s, 1H), 2.55 (s, 4H).
Aufarbeitung
- concentrationThe mixture was concentrated in vacuo
Quellen und Nachweise
- ORD-Eintrag
- ord-6e9ae33fb99744508465198838d8cd24
- Quelldatensatz
- uspto-grants-2014_05
- Patentnummer
- US08716478B2
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