N-bromobutanimide → HCID 135449959, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([CH:9]2[C:18]3[C:17](=[O:19])[CH2:16][CH2:15][CH2:14][C:13]=3[NH:12][C:11]3=[CH:20][CH:21]=[N:22][N:10]23)[CH:5]=[CH:6][C:7]=1[Cl:8].[Br:23]N1C(=O)CCC1=O>ClCCl>[Br:23][C:20]1[CH:21]=[N:22][N:10]2[CH:9]([C:4]3[CH:5]=[CH:6][C:7]([Cl:8])=[C:2]([Cl:1])[CH:3]=3)[C:18]3[C:17](=[O:19])[CH2:16][CH2:15][CH2:14][C:13]=3[NH:12][C:11]=12Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The product from Example 6 (0.52 g, 1.56 mmol) in dichloromethane was treated with N-bromosuccinimide (0.28 mg, 1.56 mmol) and allowed to stir at ambient temperature overnight. The mixture was filtered and the filter cake washed with CH2Cl2 to provide the title compound (0.54 g) as a solid.
Workup
- filtrationThe mixture was filtered
- washthe filter cake washed with CH2Cl2
Sources & evidence
- ORD record
- ord-6404f7be25d04e4f97fc77cd3c49b62c
- Source dataset
- uspto-grants-2003_03
- Patent number
- US06538000B1
Reaction notes
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