1-Ethyl-2-methoxymethyl-3-benzyloxy-6-methyl-pyridin-4(1H)-one hydrochloride → 1-Ethyl-2-methoxymethyl-3-hydroxy-6-methyl-pyridin-4(1H)-one hydrochloride
Reaction equation
[ClH:1].CN1C(C)=CC(=O)C(O)=C1COC.Cl.[CH2:16]([N:18]1[C:23]([CH3:24])=[CH:22][C:21](=[O:25])[C:20]([O:26]CC2C=CC=CC=2)=[C:19]1[CH2:34][O:35][CH3:36])[CH3:17]>[Pd]>[ClH:1].[CH2:16]([N:18]1[C:23]([CH3:24])=[CH:22][C:21](=[O:25])[C:20]([OH:26])=[C:19]1[CH2:34][O:35][CH3:36])[CH3:17]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
In an analogous hydrogenation procedure in the preparation of 1,6-dimethyl-2-methoxymethyl-3-hydroxy-pyridin-4(1H)-one hydrochloride using 1-ethyl-2-methoxymethyl-3-benzyloxy-6-methyl-pyridin-4(1H)-one hydrochloride (1.3 g, 4 mmol) and 5% Pd/C catalyst (0.3 g) yield the title compound 0.78 g (83%) after recrystallisation from methanol/diethyl ether, as a white crystalline solid. m.p. 174-176° C.
Sources & evidence
- ORD record
- ord-6f20542ba1af4a37b803c28e51aaf8d8
- Source dataset
- uspto-grants-2002_01
- Patent number
- US06335353B1
Reaction notes
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