Reaction equation
[C:1]([O:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14]O)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:16]([N:24]1[C:29](=[O:30])[CH:28]=[CH:27][NH:26][C:25]1=[O:31])(=[O:23])[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1>>[C:16]([N:24]1[C:29](=[O:30])[CH:28]=[CH:27][N:26]([CH2:14][CH2:13][CH2:12][CH2:11][CH2:10][O:9][C:1](=[O:8])[C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=2)[C:25]1=[O:31])(=[O:23])[C:17]1[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=1Participants
3
Procedure
The title compound (50%) was prepared as described in example 15 but using the alcohol 20 instead of 14 in the coupling reaction with N3-benzoyluracil.
Sources & evidence
- ORD record
- ord-54b93a12a5544175ae0a9a3cf44e89cf
- Source dataset
- uspto-grants-2010_09
- Patent number
- US07795270B2
Linked notes
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