Chlorosuccinimide → HCID 67226591, compound
Reaction equation
[CH3:1][O:2][C:3](=[O:42])[C:4]1[CH:9]=[CH:8][C:7]([N:10]2[CH2:15][CH2:14][N:13]([CH2:16][C:17]3[CH2:22][CH2:21][C:20]([CH3:24])([CH3:23])[CH2:19][C:18]=3[C:25]3[CH:30]=[CH:29][C:28]([Cl:31])=[CH:27][CH:26]=3)[CH2:12][CH2:11]2)=[CH:6][C:5]=1[O:32][C:33]1[CH:41]=[CH:40][CH:39]=[C:38]2[C:34]=1[CH:35]=[N:36][NH:37]2.[Cl:43]N1C(=O)CCC1=O>C(#N)C>[NH:37]1[C:38]2[C:34](=[C:33]([O:32][C:5]3[CH:6]=[C:7]([N:10]4[CH2:15][CH2:14][N:13]([CH2:16][C:17]5[CH2:22][CH2:21][C:20]([CH3:24])([CH3:23])[CH2:19][C:18]=5[C:25]5[CH:30]=[CH:29][C:28]([Cl:31])=[CH:27][CH:26]=5)[CH2:12][CH2:11]4)[C:8]([Cl:43])=[CH:9][C:4]=3[C:3]([O:2][CH3:1])=[O:42])[CH:41]=[CH:40][CH:39]=2)[CH:35]=[N:36]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of EXAMPLE 400D (0.5 g) and 1-chloropyrrolidine-2,5-dione (0.126 g) in acetonitrile (10 mL) was stirred at room temperature for 4 hours. The solvent was removed, and the residue was purified by flash column chromatography on silica gel to give the title compound.
Workup
- customThe solvent was removed
- customthe residue was purified by flash column chromatography on silica gel
Sources & evidence
- ORD record
- ord-2b239df6f8d245d58714c36c8fa0867b
- Source dataset
- uspto-grants-2013_11
- Patent number
- US08586754B2
Reaction notes
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