2-bromo-5-(bromomethyl)thiazole → HCID 22905805, compound
Reaction equation
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([NH:10][N:11]2[CH:15]=[N:14][N:13]=[CH:12]2)=[CH:6][CH:5]=1)([O-:3])=[O:2].[Br:16][C:17]1[S:18][C:19]([CH2:22]Br)=[CH:20][N:21]=1>>[Br:16][C:17]1[S:18][C:19]([CH2:22][N:10]([N:11]2[CH:15]=[N:14][N:13]=[CH:12]2)[C:7]2[CH:6]=[CH:5][C:4]([N+:1]([O-:3])=[O:2])=[CH:9][CH:8]=2)=[CH:20][N:21]=1Participants
3
Procedure
Starting Compounds: 4-(4-nitrophenyl)amino-4H-1,2,4-triazole and 2-bromo-5-(bromomethyl)thiazole
Sources & evidence
- ORD record
- ord-e7dc49ef562d4db787822614fc783983
- Source dataset
- uspto-grants-1997_10
- Patent number
- US05674886
Reaction notes
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