Sodium borohydride → 2-(3-ethoxy-4-methoxybenzyl)-7-[1-(1-hydroxyethyl)-4-phenylbutyl]-5-methylimidazo[5,1-f]-[1,2,4]triazin-4(3H)-one
Reaction equation
[C:1]([CH:4]([C:14]1[N:22]2[C:17]([C:18](=[O:35])[NH:19][C:20]([CH2:23][C:24]3[CH:29]=[CH:28][C:27]([O:30][CH3:31])=[C:26]([O:32][CH2:33][CH3:34])[CH:25]=3)=[N:21]2)=[C:16]([CH3:36])[N:15]=1)[CH2:5][CH2:6][CH2:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)(=[O:3])[CH3:2].[BH4-].[Na+]>>[CH2:33]([O:32][C:26]1[CH:25]=[C:24]([CH:29]=[CH:28][C:27]=1[O:30][CH3:31])[CH2:23][C:20]1[NH:19][C:18](=[O:35])[C:17]2=[C:16]([CH3:36])[N:15]=[C:14]([CH:4]([CH:1]([OH:3])[CH3:2])[CH2:5][CH2:6][CH2:7][C:8]3[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=3)[N:22]2[N:21]=1)[CH3:34]Participants
3
Procedure
58 mg (0.12 mmol) of 7-(1-acetyl-4-phenylbutyl)-2-(3-ethoxy-4-methoxybenzyl)-5-methylimidazo[5,1-f][1,2,4]triazin-4(3H)-one are reacted analogously to Example 12 with 5 mg (0.12 mmol) of sodium borohydride to give 2-(3-ethoxy-4-methoxybenzyl)-7-[1-(1-hydroxyethyl)-4-phenylbutyl]-5-methylimidazo[5,1-f]-[1,2,4]triazin-4(3H)-one.
Sources & evidence
- ORD record
- ord-39cfeef5ebcf4ada89a19a6852f9efb3
- Source dataset
- uspto-grants-2003_06
- Patent number
- US06573263B2
Reaction notes
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