Benzyl Alcohol → HCID 18317937, compound
Reaction equation
[ClH:1].[CH3:2][O:3][C:4]1[CH:5]=[C:6]2[C:14](=[CH:15][CH:16]=1)[NH:13][C:12]1[CH:11]([C:17]3([C:21]([O:23][CH2:24][CH3:25])=[O:22])[CH2:20][CH2:19][CH2:18]3)[NH:10][CH2:9][CH2:8][C:7]2=1.C(O)[C:27]1[CH:32]=[CH:31]C=[CH:29][CH:28]=1>>[ClH:1].[CH3:2][O:3][C:4]1[CH:5]=[C:6]2[C:14](=[CH:15][CH:16]=1)[NH:13][C:12]1[CH:11]([C:17]3([C:21]([O:23][CH2:24][C:25]4[CH:31]=[CH:32][CH:27]=[CH:28][CH:29]=4)=[O:22])[CH2:20][CH2:19][CH2:18]3)[NH:10][CH2:9][CH2:8][C:7]2=1Participants
3
Procedure
The procedure is as in Example 23, using as substrate the product of Example 7 and as reagent benzyl alcohol.
Sources & evidence
- ORD record
- ord-99863bcb6a7f41cf9c7ccaeef584dec7
- Source dataset
- uspto-grants-2002_02
- Patent number
- US06350757B1
Reaction notes
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