Bromoacetyl bromide → HCID 66645692, compound
Reaction equation
[Br:1][CH2:2][C:3](Br)=[O:4].[C:6]([O:10][C:11](=[O:26])[NH:12][C:13]([CH3:25])([CH3:24])[CH2:14][NH:15][C:16]1[CH:21]=[CH:20][CH:19]=[C:18]([F:22])[C:17]=1[CH3:23])([CH3:9])([CH3:8])[CH3:7].C(=O)(O)[O-].[Na+]>CN(C)C(=O)C>[C:6]([O:10][C:11](=[O:26])[NH:12][C:13]([CH3:25])([CH3:24])[CH2:14][N:15]([C:3](=[O:4])[CH2:2][Br:1])[C:16]1[CH:21]=[CH:20][CH:19]=[C:18]([F:22])[C:17]=1[CH3:23])([CH3:9])([CH3:8])[CH3:7]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
1.4 ml of bromoacetyl bromide (16.1 mmol) was added to a solution of 3.97 g of [1,1-dimethyl-2-(3-fluoro-2-methylphenylamino)ethyl]carbamic acid t-butyl ester obtained in Example (67a) (13.4 mmol) in N,N-dimethylacetamide (67 ml) under ice-cooling, and the mixture was stirred at the same temperature for 10 minutes. A saturated sodium bicarbonate aqueous solution was added to the reaction mixture, followed by extraction with ethyl acetate. Then, the organic layer was washed with water and brine and dried over anhydrous magnesium sulfate. After filtration, the solvent was evaporated under reduced pressure. Hexane was added to the residue, and the solid was collected by filtration to obtain 4.23 g of the title compound (yield: 76%).
Workup
- temperaturecooling
- extractionfollowed by extraction with ethyl acetate
- washThen, the organic layer was washed with water and brine
- dry with materialdried over anhydrous magnesium sulfate
- filtrationAfter filtration
- customthe solvent was evaporated under reduced pressure
- additionHexane was added to the residue
- filtrationthe solid was collected by filtration
Sources & evidence
- ORD record
- ord-4725476d691a4d369971dc83e69b0ef6
- Source dataset
- uspto-grants-2012_04
- Patent number
- US08158790B2
Reaction notes
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