Methyl 6-pyrrolidinonicotinate → 6-(Pyrrolidin-1-yl)nicotinic acid
Reaction equation
[N:1]1([C:6]2[CH:15]=[CH:14][C:9]([C:10]([O:12]C)=[O:11])=[CH:8][N:7]=2)[CH2:5][CH2:4][CH2:3][CH2:2]1>Cl>[N:1]1([C:6]2[CH:15]=[CH:14][C:9]([C:10]([OH:12])=[O:11])=[CH:8][N:7]=2)[CH2:2][CH2:3][CH2:4][CH2:5]1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 40 °C
Procedure
1.0 g (4.85 mol) of methyl 6-(pyrrolidine-1-yl)nicotinoate was dissolved in 10 ml of conc. hydrochloric acid and stirred at 40° C. overnight. The solvent was distilled off whereby the hydrochloride of the title compound was obtained.
Workup
- distillationThe solvent was distilled off whereby the hydrochloride of the title compound
- customwas obtained
Sources & evidence
- ORD record
- ord-55c46c1b6dc24d8aa997a33dcc511499
- Source dataset
- uspto-grants-2008_07
- Patent number
- US07396844B1
Reaction notes
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