5-tert-Butyl-o-anisidine → N-(5-tert-Butyl-2-methoxy-phenyl)-3-[4-(5-ethyl-1-phenyl-1H-pyrazol-4-yl)-imidazol-1-yl]-4-methyl-benzamide

HRID 2109305Notes

Reaction equation

HRID 2109305 reaction equation
[C:1]([C:5]1[CH:6]=[CH:7][C:8]([O:12][CH3:13])=[C:9]([NH2:11])[CH:10]=1)([CH3:4])([CH3:3])[CH3:2].C[O:15][C:16](=O)[C:17]1[CH:22]=[CH:21][C:20]([CH3:23])=[C:19]([N:24]2[CH:28]=[C:27]([C:29]3[CH:30]=[N:31][N:32]([C:36]4[CH:41]=[CH:40][CH:39]=[CH:38][CH:37]=4)[C:33]=3[CH2:34][CH3:35])[N:26]=[CH:25]2)[CH:18]=1>>[C:1]([C:5]1[CH:6]=[CH:7][C:8]([O:12][CH3:13])=[C:9]([NH:11][C:16](=[O:15])[C:17]2[CH:22]=[CH:21][C:20]([CH3:23])=[C:19]([N:24]3[CH:28]=[C:27]([C:29]4[CH:30]=[N:31][N:32]([C:36]5[CH:41]=[CH:40][CH:39]=[CH:38][CH:37]=5)[C:33]=4[CH2:34][CH3:35])[N:26]=[CH:25]3)[CH:18]=2)[CH:10]=1)([CH3:4])([CH3:2])[CH3:3]

Participants

3

Procedure

Example 153 was prepared from 5-tert-butyl-2-methoxy-phenylamine and 3-[4-(5-ethyl-1-phenyl-1H-pyrazol-4-yl)-imidazol-1-yl]-4-methyl-benzoic acid methyl ester (Example 151) in the same manner as Example 151. ESI MS m/z 534 [C33H35N5O2+H]1.

Sources & evidence

ORD record
ord-a12db1b69be44ab1bcfe6e69d929fe93
Source dataset
uspto-grants-2009_04
Patent number
US07514458B2

Reaction notes

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