5-Bromosalicylic acid → HCID 10044517, compound
Reaction equation
[Br:1][C:2]1[CH:10]=[C:6]([C:7]([OH:9])=O)[C:5]([OH:11])=[CH:4][CH:3]=1.[NH2:12][C:13]1[S:14][C:15]([C:18]([F:21])([F:20])[F:19])=[N:16][N:17]=1>>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([OH:11])=[C:6]([CH:10]=1)[C:7]([NH:12][C:13]1[S:14][C:15]([C:18]([F:21])([F:20])[F:19])=[N:16][N:17]=1)=[O:9]Participants
3
Procedure
Using 5-bromosalicylic acid and 2-amino-5-(trifluoromethyl)-1,3,4-thiadiazole as the raw materials, the same operation as the example 16 gave the title compound.
Sources & evidence
- ORD record
- ord-19a59145cd0048309b2aebd5d88be6a3
- Source dataset
- uspto-grants-2012_09
- Patent number
- US08263657B2
Reaction notes
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