Sodium Hydroxide → HCID 18172495, compound
Reaction equation
[CH2:1]([N:4]1[C:9](=[O:10])[C:8]([C:11]([O:13]CC)=[O:12])=[CH:7][N:6]=[CH:5]1)[CH:2]=[CH2:3].[OH-].[Na+]>CO.O>[CH2:1]([N:4]1[C:9](=[O:10])[C:8]([C:11]([OH:13])=[O:12])=[CH:7][N:6]=[CH:5]1)[CH:2]=[CH2:3]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
To the compound of Example 21 (5.00 g, 0.024 mole), suspended in methanol (25 mL) and cooled in an ice bath, 1.0N NaOH (29 mL, 0.029 mole) is added dropwise rapidly with stirring. After 16 hours, the solvent is reduced under vacuum, residue diluted with water (50 mL), and washed with ethyl acetate (2×15 mL). The aqueous layer is acidified with 2.0N HCl to pH 1, extracted with ethyl acetate (3×50 mL). The combined organic extracts are washed with water, then brine (twice). The solvent is removed in vacuo to afford the title compound.
Workup
- temperaturecooled in an ice bath
- washwashed with ethyl acetate (2×15 mL)
- extractionextracted with ethyl acetate (3×50 mL)
- washThe combined organic extracts are washed with water
- customThe solvent is removed in vacuo
Sources & evidence
- ORD record
- ord-0f90cae910b64e1481167bf65b2c71c0
- Source dataset
- uspto-grants-2003_08
- Patent number
- US06608204B1
Reaction notes
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