Tert-Butylamine → 5-(tert-Butyl)-3-((tert-butylamino)methyl)-2',4'-dichloro-[1,1'-biphenyl]-2-ol hydrochloride
Reaction equation
[C:1]([C:5]1[CH:6]=[C:7]([CH:20]=O)[C:8]([OH:19])=[C:9]([C:11]2[CH:16]=[CH:15][C:14]([Cl:17])=[CH:13][C:12]=2[Cl:18])[CH:10]=1)([CH3:4])([CH3:3])[CH3:2].[C:22]([NH2:26])([CH3:25])([CH3:24])[CH3:23]>>[ClH:17].[C:1]([C:5]1[CH:10]=[C:9]([C:11]2[CH:16]=[CH:15][C:14]([Cl:17])=[CH:13][C:12]=2[Cl:18])[C:8]([OH:19])=[C:7]([CH2:20][NH:26][C:22]([CH3:25])([CH3:24])[CH3:23])[CH:6]=1)([CH3:4])([CH3:3])[CH3:2]Participants
3
Procedure
5-(tert-Butyl)-3-((tert-butylamino)methyl)-2′,4′-dichloro-[1,1′-biphenyl]-2-ol hydrochloride was prepared as a gray solid using the procedure described in Example 9 from 5-(tert-butyl)-2′,4′-dichloro-2-hydroxy-[1,1′-biphenyl]-3-carbaldehyde and tert-butylamine.
Sources & evidence
- ORD record
- ord-be303eee24a14743abc7b33278b948ab
- Source dataset
- uspto-grants-2016_03
- Patent number
- US09296696B2
Reaction notes
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