Hydrogen Bromide → HCID 118106272, compound
Reaction equation
[CH3:1][NH:2][C:3]1[N:8]=[CH:7][C:6]([C:9](=[O:11])[CH3:10])=[CH:5][CH:4]=1.[BrH:12].BrBr>C(O)(=O)C>[Br:12][CH2:10][C:9]([C:6]1[CH:7]=[N:8][C:3]([NH:2][CH3:1])=[CH:4][CH:5]=1)=[O:11]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
380 mg (2.53 mmol) of 1-(6-methylaminopyrid-3-yl)ethanone, 416 μl (2.53 mmol) of hydrobromic acid, 130 μl (2.53 mmol) of bromine and 5 mL of glacial acetic acid were used in the reaction. After precipitation with ethyl ether and filtration, the precipitate is taken up in water. The solution is basified with saturated NaHCO3 solution. The precipitate formed is filtered off, washed with water and then dried under vacuum. 370 mg of 2-bromo-1-(6-methylaminopyrid-3-yl)ethanone are obtained, the characteristics of which are as follows:
Workup
- customAfter precipitation
- filtrationwith ethyl ether and filtration
- customThe precipitate formed
- filtrationis filtered off
- washwashed with water
- customdried under vacuum
Sources & evidence
- ORD record
- ord-1dfc804ed41f4ac993b9d14f314b2b1f
- Source dataset
- uspto-grants-2016_04
- Patent number
- US09321790B2
Reaction notes
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