4-Tert-Butylaniline → HCID 36839778, compound
Reaction equation
[N:1]1([CH2:10][CH2:11][C:12]([OH:14])=O)[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[CH:2]1.[C:15]([C:19]1[CH:25]=[CH:24][C:22]([NH2:23])=[CH:21][CH:20]=1)([CH3:18])([CH3:17])[CH3:16]>>[N:1]1([CH2:10][CH2:11][C:12]([NH:23][C:22]2[CH:24]=[CH:25][C:19]([C:15]([CH3:18])([CH3:17])[CH3:16])=[CH:20][CH:21]=2)=[O:14])[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 3-benzoimidazol-1-yl-propanoic acid and 4-tert-butyl-aniline. Calculated for C16H23N3O m/z: 321.18, found 322.1 [M+H]+.
Sources & evidence
- ORD record
- ord-9d519a5abad44fddb1d30b8e2edf66fd
- Source dataset
- uspto-grants-2010_01
- Patent number
- US07645784B2
Reaction notes
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