2-Cyclopropyl-5-phenyl-oxazole-4-carboxylic acid → HCID 49834425, 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)[S:8][CH:9]=1)([F:4])[CH3:3].[CH:17]1([C:20]2[O:21][C:22]([C:28]3[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=3)=[C:23]([C:25](O)=[O:26])[N:24]=2)[CH2:19][CH2:18]1>>[F:1][C:2]([C:5]1[N:6]=[C:7]([CH2:10][N:11]2[N:15]=[C:14]([NH:16][C:25]([C:23]3[N:24]=[C:20]([CH:17]4[CH2:18][CH2:19]4)[O:21][C:22]=3[C:28]3[CH:29]=[CH:30][CH:31]=[CH:32][CH:33]=3)=[O:26])[CH:13]=[N:12]2)[S:8][CH:9]=1)([F:4])[CH3:3]Participants
3
Procedure
Following general procedure Z2, starting from 2-[4-(1,1-difluoro-ethyl)-thiazol-2-ylmethyl]-2H-[1,2,3]triazol-4-ylamine and 2-cyclopropyl-5-phenyl-oxazole-4-carboxylic acid.
Sources & evidence
- ORD record
- ord-c92c255ba5654763b68e289f337b5545
- Source dataset
- uspto-grants-2013_11