2-Amino-5-methylpyridine → HCID 57438623, compound
Reaction equation
[C:1]([O:5]C)(=O)[CH2:2][OH:3].[NH2:7][C:8]1[CH:13]=[CH:12][C:11]([CH3:14])=[CH:10][N:9]=1>>[OH:3][CH2:2][C:1]([NH:7][C:8]1[CH:13]=[CH:12][C:11]([CH3:14])=[CH:10][N:9]=1)=[O:5]Participants
3
Procedure
The title compound was prepared in a manner similar to that described for Intermediate A3, starting from methyl glycolate and 2-amino-5-picoline, 1H NMR (300 MHz, CDCl3) δ 9.24 (br s, 1H), 8.19 (d, 1H), 8.07 (d, 1H), 7.57 (dd, 1H), 5.59 (br s, 1H), 4.26 (s, 2H), 2.31 (s, 3H).
Sources & evidence
- ORD record
- ord-6e052183311c46949f9767716ccbd8ba
- Source dataset
- uspto-grants-2012_03
- Patent number
- US08143263B2
Reaction notes
Loading…