Hydrogen Bromide → HCID 67164022, compound
Reaction equation
[CH3:1][C:2]1[C:3]([C:12]([OH:14])=[O:13])=[N:4][C:5]([CH3:11])=[CH:6][C:7]=1[N+]([O-])=O.[BrH:15]>>[Br:15][C:7]1[CH:6]=[C:5]([CH3:11])[N:4]=[C:3]([C:12]([OH:14])=[O:13])[C:2]=1[CH3:1]Participants
3
Procedure
The title compound, was prepared by treatment of 3,6-Dimethyl-4-nitro-pyridine-2-carboxylic acid with 49% hydrobrornic acid at 101° C. in accordance with the general method of example 1, step 3 to yield the title compound as an amorphous yellow solid, which is directly used in the next step without further purification.
Sources & evidence
- ORD record
- ord-93d39c7b79b14079b03fa95f38cb4561
- Source dataset
- uspto-grants-2011_05
- Patent number
- US07951824B2
Reaction notes
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