1-methyl-1H-pyrazol-4-amine → 5-amino-N-(1-methyl-1H-pyrazol-4-yl)thiazole-4-carboxamide
Reaction equation
[CH3:1][N:2]1[CH:6]=[C:5]([NH2:7])[CH:4]=[N:3]1.C(OC([NH:15][C:16]1[S:20][CH:19]=[N:18][C:17]=1[C:21](O)=[O:22])=O)(C)(C)C>>[NH2:15][C:16]1[S:20][CH:19]=[N:18][C:17]=1[C:21]([NH:7][C:5]1[CH:4]=[N:3][N:2]([CH3:1])[CH:6]=1)=[O:22]Participants
3
Procedure
Following the procedures as described in Example 113, 1-methyl-1H-pyrazol-4-amine, 5-(tert-butoxycarbonylamino)thiazole-4-carboxylic acid were reacted to give 5-amino-N-(1-methyl-1H-pyrazol-4-yl)thiazole-4-carboxamide as a white solid (13 mg, 32%) over two steps. ESIMS m/z=336.1 (M+1)
Workup
- customwere reacted
Sources & evidence
- ORD record
- ord-80d0d4fd85a049ce998fe5bf22c53322
- Source dataset
- uspto-grants-2014_03
- Patent number
- US08669361B2
Reaction notes
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