Bromine → HCID 87110339, compound
Reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([Br:11])[C:5]2[N:6]([CH:8]=[CH:9][N:10]=2)[N:7]=1.[Br:12]Br>C(O)(=O)C>[Br:12][C:8]1[N:6]2[N:7]=[C:2]([Br:1])[CH:3]=[C:4]([Br:11])[C:5]2=[N:10][CH:9]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a stirred suspension of 100.00 g (361.1 mmol) 6,8-dibromoimidazo[1,2-b]pyridazine, which was prepared according to intermediate example 96d, in 1.6 L acetic acid were added 69.2 g (433.3 mmol) bromine at it and the mixture was stirred for 1 h. The precipitate was filtered, washed with water and dissolved in 10 L DCM. The organic üphase was washed with saturated sodium hydrogen carbonate solution, dried over sodium sulfate, filtered and evaporated to give 81.99 g (64%) of the title compound.
Workup
- customwas prepared
- filtrationThe precipitate was filtered
- washwashed with water
- dissolutiondissolved in 10 L DCM
- washThe organic üphase was washed with saturated sodium hydrogen carbonate solution
- dry with materialdried over sodium sulfate
- filtrationfiltered
- customevaporated
Sources & evidence
- ORD record
- ord-4a93771476534ec9aab1f3f86c2fd8a1
- Source dataset
- uspto-grants-2016_02
- Patent number
- US09255100B2
Reaction notes
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