Imidazole → 2-(Imidazol-1-ylmethyl)-3-hydroxy-4-methylpyridine
Reaktionsgleichung
[CH3:1][N:2]([CH2:4][C:5]1[C:10]([OH:11])=[C:9]([CH3:12])[CH:8]=[CH:7][N:6]=1)[CH3:3].[NH:13]1C=CN=[CH:14]1>C1(C)C(C)=CC=CC=1>[N:2]1([CH2:4][C:5]2[C:10]([OH:11])=[C:9]([CH3:12])[CH:8]=[CH:7][N:6]=2)[CH:1]=[CH:14][N:13]=[CH:3]1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
The procedure described in Example 1 was then repeated except that 2-dimethylaminomethyl-3-hydroxy-4-methylpyridine (4.44 g.) and imidazole (1.82 g.) were reacted in xylene (15 ml.) to afford 2-(imidazol-1-ylmethyl)-3-hydroxy-4-methylpyridine (yield, 3.60 g.), m.p. 170°-172° C. after recrystallization from toluene.
Quellen und Nachweise
- ORD-Eintrag
- ord-819b2155e7864cdfb09631673adb5f36
- Quelldatensatz
- uspto-grants-1980_10
- Patentnummer
- US04230714
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