HCID 15729334, compound → HCID 22252357, compound
Reaction equation
[CH2:1]([NH:8][C:9]1[CH:14]=[C:13]([O:15][CH3:16])[C:12]([O:17][CH3:18])=[C:11]([O:19][CH3:20])[CH:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH2:21]1[N:26]([CH2:27][CH2:28][CH2:29][C:30](O)=[O:31])[CH2:25][CH2:24][N:23]2[CH2:33][CH2:34][CH2:35][CH2:36][CH:22]12>>[CH2:1]([N:8]([C:9]1[CH:14]=[C:13]([O:15][CH3:16])[C:12]([O:17][CH3:18])=[C:11]([O:19][CH3:20])[CH:10]=1)[C:30](=[O:31])[CH2:29][CH2:28][CH2:27][N:26]1[CH2:25][CH2:24][N:23]2[CH2:33][CH2:34][CH2:35][CH2:36][CH:22]2[CH2:21]1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1Participants
3
Procedure
The procedure is as for Example 2 using as substrate benzyl-(3,4,5-trimethoxyphenyl)-amine and the compound obtained in Step B of Example 2.
Sources & evidence
- ORD record
- ord-fb8f33e39d2b422c8422674c5e1d353e
- Source dataset
- uspto-grants-2006_01
- Patent number
- US06992085B2
Reaction notes
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