Hydrochloric Acid → 2-(Isopropylamino)-6-methylisonicotinic acid hydrochloride
Reaction equation
C([O:3][C:4](=[O:16])[C:5]1[CH:10]=[C:9]([CH3:11])[N:8]=[C:7]([NH:12][CH:13]([CH3:15])[CH3:14])[CH:6]=1)C.[ClH:17]>>[ClH:17].[CH:13]([NH:12][C:7]1[CH:6]=[C:5]([CH:10]=[C:9]([CH3:11])[N:8]=1)[C:4]([OH:16])=[O:3])([CH3:15])[CH3:14]Participants
3
Procedure
A solution of 2-isopropylamino-6-methyl-isonicotinic acid ethyl ester (3.90 g, 17.5 mmol) in 32% aq. HCl (100 mL) is stirred at 70° C. for 5 h before it is cooled to rt and concentrated. The residue is dried under HV to give 2-isopropylamino-6-methyl-isonicotinic acid hydrochloride (4.20 g) as an orange resin; LC-MS: tR=0.52 min; [M+1]+=195.09.
Workup
- concentrationconcentrated
- customThe residue is dried under HV
Sources & evidence
- ORD record
- ord-3d3c435b463740ea9e78b187b51aa0cc
- Source dataset
- uspto-grants-2013_12
- Patent number
- US08598208B2
Reaction notes
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