Sodium Hydroxide → HCID 66597201, compound
Reaction equation
[CH3:1][C:2]1[N:7]=[C:6]2[S:8][CH:9]=[CH:10][C:5]2=[C:4]([C:11]2[CH:16]=[CH:15][C:14]([CH3:17])=[CH:13][CH:12]=2)[C:3]=1[CH:18]([CH2:23][CH2:24][CH3:25])[C:19]([O:21]C)=[O:20].[OH-].[Na+]>CO.C(O)C>[CH3:1][C:2]1[N:7]=[C:6]2[S:8][CH:9]=[CH:10][C:5]2=[C:4]([C:11]2[CH:12]=[CH:13][C:14]([CH3:17])=[CH:15][CH:16]=2)[C:3]=1[CH:18]([CH2:23][CH2:24][CH3:25])[C:19]([OH:21])=[O:20]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
To a solution of methyl 2-(6-methyl-4-p-tolylthieno[2,3-b]pyridin-5-yl)pentanoate (0.051 g; 0.144 mmol) in methanol (3 mL) and ethanol (1.5 mL) was added a 5% sodium hydroxide solution (3.9 mL; 4.875 mmol). The reaction mixture was heated under reflux for 4 h. After cooling to room temperature, the reaction mixture was concentrated under reduced pressure. The residue was suspended in water, acidified with 1N HCl (pH˜2) and extracted with ethyl acetate. The organic layer was washed with water and brine, dried over sodium sulphate, filtered and concentrated under reduced pressure. The residue was crystallized from a mixture of ethyl acetate/heptane to afford 0.027 g (55%) of the title compound as a white solid.
Workup
- temperatureThe reaction mixture was heated
- temperatureunder reflux for 4 h
- concentrationthe reaction mixture was concentrated under reduced pressure
- extractionextracted with ethyl acetate
- washThe organic layer was washed with water and brine
- dry with materialdried over sodium sulphate
- filtrationfiltered
- concentrationconcentrated under reduced pressure
- customThe residue was crystallized from a mixture of ethyl acetate/heptane
Sources & evidence
- ORD record
- ord-069dd3922935400b896dba991ccfb886
- Source dataset
- uspto-grants-2014_07
- Patent number
- US08785638B2
Reaction notes
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