Tert-Butylamine → HCID 86718741, compound
Reaction equation
[C:1]([C:5]1[CH:6]=[C:7]([CH:22]=O)[C:8]([OH:21])=[C:9]([C:11]2[CH:16]=[CH:15][CH:14]=[C:13]([C:17]([F:20])([F:19])[F:18])[CH:12]=2)[CH:10]=1)([CH3:4])([CH3:3])[CH3:2].[C:24]([NH2:28])([CH3:27])([CH3:26])[CH3:25]>>[C:1]([C:5]1[CH:10]=[C:9]([C:11]2[CH:16]=[CH:15][CH:14]=[C:13]([C:17]([F:20])([F:19])[F:18])[CH:12]=2)[C:8]([OH:21])=[C:7]([CH2:22][NH:28][C:24]([CH3:27])([CH3:26])[CH3:25])[CH:6]=1)([CH3:2])([CH3:3])[CH3:4]Participants
3
Procedure
5-(tert-Butyl)-3-((tert-butylamino)methyl)-3′-(trifluoromethyl)-[1,1′-biphenyl]-2-ol was prepared as a white solid using the procedure described in Example 27, Step 2 5-(tert-butyl)-2-hydroxy-3′-(trifluoromethyl)-[1,1′-biphenyl]-3-carbaldehyde and tert-butylamine HPLC/MS Rt=6.64 min, m/z 380.2 (M+H+).
Sources & evidence
- ORD record
- ord-4e51efdae2c94190a37d1e68857c4bd2
- Source dataset
- uspto-grants-2015_02
- Patent number
- US08962657B2
Reaction notes
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