2-Amino-5-methylpyridine → HCID 3419927, compound
Reaction equation
[Br:1][CH2:2][C:3](Br)=[O:4].[NH2:6][C:7]1[CH:12]=[CH:11][C:10]([CH3:13])=[CH:9][N:8]=1>>[Br:1][CH2:2][C:3]([NH:6][C:7]1[CH:12]=[CH:11][C:10]([CH3:13])=[CH:9][N:8]=1)=[O:4]Participants
3
Procedure
The title compound was prepared in a manner similar to that described for Intermediate A16 (Step 5) starting from bromoacetyl bromide and 2-amino-5-picoline.
Sources & evidence
- ORD record
- ord-ec65c6cb9ea741c3ba9eafd2d08929e4
- Source dataset
- uspto-grants-2012_03
- Patent number
- US08143263B2
Reaction notes
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