Succinic anhydride → HCID 178512849, compound
Reaction equation
[NH2:1][C:2]1[CH:21]=[CH:20][C:5]([C:6]([NH:8][C@H:9]([C:17](=[O:19])[NH2:18])[CH2:10][CH2:11][CH2:12][NH:13][C:14]([NH2:16])=[NH:15])=[O:7])=[CH:4][C:3]=1[O:22][CH2:23][CH2:24][C:25]1[CH:30]=[CH:29][C:28]([Cl:31])=[CH:27][C:26]=1[Cl:32].[C:33]1(=[O:39])[O:38][C:36](=[O:37])[CH2:35][CH2:34]1>>[C:17]([C@@H:9]([NH:8][C:6]([C:5]1[CH:20]=[CH:21][C:2]([NH:1][C:33](=[O:39])[CH2:34][CH2:35][C:36]([OH:38])=[O:37])=[C:3]([O:22][CH2:23][CH2:24][C:25]2[CH:30]=[CH:29][C:28]([Cl:31])=[CH:27][C:26]=2[Cl:32])[CH:4]=1)=[O:7])[CH2:10][CH2:11][CH2:12][NH:13][C:14]([NH2:16])=[NH:15])(=[O:19])[NH2:18]Participants
3
Procedure
The third part of the resin obtained in Example 2 (116 mg) was coupled with 160 mg of succinic anhydride analogously to the procedure described in Example 3. The resin was washed and dried, and the final product was cleaved off and processed as described in Example 1.
Workup
- washThe resin was washed
- customdried
Sources & evidence
- ORD record
- ord-7eb620a8c5354200b8e030b85c54c72d
- Source dataset
- uspto-grants-2002_10
- Patent number
- US06472562B1
Reaction notes
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