HCID 67127742, compound → HCID 49834428, compound
Reaction equation
[F:1][C:2]([C:5]1[N:6]=[C:7]([CH2:10][N:11]2[N:15]=[C:14]([NH2:16])[CH:13]=[N:12]2)[O:8][CH:9]=1)([F:4])[CH3:3].[CH3:17][N:18]([CH3:34])[C:19]1[CH:20]=[C:21]([C:26]2[O:30][CH:29]=[N:28][C:27]=2[C:31](O)=[O:32])[CH:22]=[CH:23][C:24]=1[F:25]>>[F:1][C:2]([C:5]1[N:6]=[C:7]([CH2:10][N:11]2[N:15]=[C:14]([NH:16][C:31]([C:27]3[N:28]=[CH:29][O:30][C:26]=3[C:21]3[CH:22]=[CH:23][C:24]([F:25])=[C:19]([N:18]([CH3:34])[CH3:17])[CH:20]=3)=[O:32])[CH:13]=[N:12]2)[O:8][CH:9]=1)([F:4])[CH3:3]Participants
3
Procedure
Following general procedure A, starting from 2-[4-(1,1-difluoro-ethyl)-oxazol-2-ylmethyl]-2H-[1,2,3]triazol-4-ylamine and 5-(3-(dimethylamino)-4-fluorophenyl)oxazole-4-carboxylic acid.
Sources & evidence
- ORD record
- ord-5cb254fe910649f0aa2b08f50d3a4eb7
- Source dataset
- uspto-grants-2013_11
- Patent number
- US08580831B2
Reaction notes
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