Sodium borohydride → (+/-)-7-Chloro-1-((imidazol-4-yl)ethyl)-2-methyl-4h-benzo[5,6]cyclohepta[1,2-d]imidazol-4-ol
Reaction equation
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[C:22](=[O:23])[C:10]3[N:11]=[C:12]([CH3:21])[N:13]([CH2:14][CH2:15][C:16]4[N:17]=[CH:18][NH:19][CH:20]=4)[C:9]=3[CH:8]=[CH:7][C:6]=2[CH:24]=1.[BH4-].[Na+]>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[CH:22]([OH:23])[C:10]3[N:11]=[C:12]([CH3:21])[N:13]([CH2:14][CH2:15][C:16]4[N:17]=[CH:18][NH:19][CH:20]=4)[C:9]=3[CH:8]=[CH:7][C:6]=2[CH:24]=1Participants
3
Procedure
The subtitle product was prepared from the product of step (i) (0.966 g) and sodium borohydride (0.215 g) according the method of example 71 step (ii). Used directly in the next step.
Sources & evidence
- ORD record
- ord-f6fa800f083b412d93a0f287b6315d8a
- Source dataset
- uspto-grants-2001_04
- Patent number
- US06218376B1
Reaction notes
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