4-Tert-Butylaniline → HCID 68490187, compound
Reaction equation
[N:1]1([CH2:10][CH2:11][CH2:12][C:13]([OH:15])=O)[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[CH:2]1.[C:16]([C:20]1[CH:26]=[CH:25][C:23]([NH2:24])=[CH:22][CH:21]=1)([CH3:19])([CH3:18])[CH3:17]>>[N:1]1([CH2:10][CH2:11][CH2:12][C:13]([NH:24][C:23]2[CH:25]=[CH:26][C:20]([C:16]([CH3:19])([CH3:18])[CH3:17])=[CH:21][CH:22]=2)=[O:15])[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[CH:2]1Participants
3
Procedure
Part C. The title compound was synthesized according to a procedure described in Example 98 starting from 4-benzoimidazol-1-yl-butyric acid and 4-tert-butyl-aniline. Calculated for C16H23N3O m/z: 335.20, found 336.1 [M+H]+.
Sources & evidence
- ORD record
- ord-68c081d826de4271987f91ccd4f4379c
- Source dataset
- uspto-grants-2010_01
- Patent number
- US07645784B2
Reaction notes
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