Formic Acid → HCID 86633532, compound
Reaction equation
[CH:1]([OH:3])=O.Cl.[NH2:5][OH:6].[C:7]([O-])(=O)[CH3:8].[Na+].[Cl-].[Na+].[C:14]([O:17][CH2:18][CH3:19])(=O)[CH3:15]>>[CH3:1][O:3][CH2:15][C@@H:14]([O:17][CH2:18][CH:19]=[N:5][OH:6])[CH:7]=[CH2:8]Participants
6
Procedure
Formic acid (35.1 mL), hydroxylamine hydrochloride (2.83 g) and sodium acetate (4.46 g) were added to the compound obtained in Preparation Example 24-(2) (5.82 g), and the mixture was stirred at room temperature for 30 minutes. Ethyl acetate and a saturated sodium chloride solution were added to the reaction solution, and the organic layer was separated. The organic layer was washed with saturated aqueous sodium chloride and then dried over anhydrous magnesium sulfate. The insoluble matter was separated by filtration and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography to obtain the title compound (2.00 g).
Workup
- customthe organic layer was separated
- washThe organic layer was washed with saturated aqueous sodium chloride
- dry with materialdried over anhydrous magnesium sulfate
- customThe insoluble matter was separated by filtration
- concentrationthe filtrate was concentrated under reduced pressure
- customThe residue was purified by silica gel column chromatography
Sources & evidence
- ORD record
- ord-8215d3734b1b4198804d5c9f1c2bfda6
- Source dataset
- uspto-grants-2015_02
- Patent number
- US08946210B2
Reaction notes
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