P-Cresol → HCID 57799714, compound
Reaction equation
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[CH:4][CH:3]=1.Cl[C:10]1[C:19]2[C:14](=[C:15]([CH3:20])[CH:16]=[CH:17][CH:18]=2)[CH:13]=[C:12]([NH:21][C:22]2[CH:26]=[C:25]([CH3:27])[NH:24][N:23]=2)[N:11]=1>>[CH3:27][C:25]1[NH:24][N:23]=[C:22]([NH:21][C:12]2[N:11]=[C:10]([O:8][C:5]3[CH:6]=[CH:7][C:2]([CH3:1])=[CH:3][CH:4]=3)[C:19]3[C:14]([CH:13]=2)=[C:15]([CH3:20])[CH:16]=[CH:17][CH:18]=3)[CH:26]=1Participants
3
Procedure
Similar procedure as described in example 10 was used, starting from 4-methyl-phenol and (1-chloro-5-methyl-isoquinolin-3-yl)-(5-methyl-1H-pyrazol-3-yl)-amine to give (5-methyl-1H-pyrazol-3-yl)-(1-p-tolyloxy-5-methyl-isoquinolin-3-yl)-amine. LC-MS m/e 345(MH+).
Sources & evidence
- ORD record
- ord-2e453ac13b954fc98c01d5237bfa966a
- Source dataset
- uspto-grants-2009_08
- Patent number
- US07572809B2
Reaction notes
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