Cysteamine Hydrochloride → 2-(3-Bromo-4-methyl-2-pyridylmethylthio)ethylamine dihydrobromide
Reaktionsgleichung
[Br:1][C:2]1[C:3]([CH2:9]O)=[N:4][CH:5]=[CH:6][C:7]=1[CH3:8].Cl.[NH2:12][CH2:13][CH2:14][SH:15]>Br>[BrH:1].[BrH:1].[Br:1][C:2]1[C:3]([CH2:9][S:15][CH2:14][CH2:13][NH2:12])=[N:4][CH:5]=[CH:6][C:7]=1[CH3:8]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of 3-bromo-2-hydroxymethyl-4-methylpyridine (5.8), cysteamine hydrochloride (3.5 g) and hydrobromic acid (48%, 50 ml) was refluxed for 6 hours and evaporated to dryness. The residue was crystallised from isopropanol/methanol to give 2-(3-bromo-4-methyl-2-pyridylmethylthio)ethylamine dihydrobromide (8.5 g) m.p. 203°-205°.
Aufarbeitung
- temperaturewas refluxed for 6 hours
- customevaporated to dryness
- customThe residue was crystallised from isopropanol/methanol
Quellen und Nachweise
- ORD-Eintrag
- ord-f5cc995a9627401b84218b5330678505
- Quelldatensatz
- uspto-grants-1980_08
- Patentnummer
- US04216318
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