Bromine → HCID 86631783, compound
Reaction equation
[S:1]1[CH:5]=[CH:4][N:3]2[CH:6]=[C:7]([C:9]3[CH:16]=[CH:15][C:12]([CH:13]=[O:14])=[CH:11][CH:10]=3)[N:8]=[C:2]12.[Br:17]Br>C(O)(=O)C>[Br:17][C:6]1[N:3]2[C:2]([S:1][CH:5]=[CH:4]2)=[N:8][C:7]=1[C:9]1[CH:10]=[CH:11][C:12]([CH:13]=[O:14])=[CH:15][CH:16]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
4-Imidazo[2,1-b]thiazol-6-yl-benzaldehyde (3.8 g, 14.9 mM) is dissolved in 30 mL acetic acid. A solution of bromine (1.1 eq) in acetic acid (15 mL) is added to the reaction mixture. The reaction mixture is stirred for 3 h at room temperature. The solid obtained is collected by filtration and re-dissolved in water (100 ml) and the solution neutralized by aqueous ammonia. The solid obtained is collected by filtration and dried.
Workup
- customThe solid obtained
- filtrationis collected by filtration
- dissolutionre-dissolved in water (100 ml)
- customThe solid obtained
- filtrationis collected by filtration
- customdried
Sources & evidence
- ORD record
- ord-a1f9ee79ee4d46c49040f6a5dd12b931
- Source dataset
- uspto-grants-2013_11
- Patent number
- US08592591B2
Reaction notes
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