Homoveratrylamine → HCID 19838095, compound
Reaction equation
[C:1]1([CH2:7][CH2:8][NH:9][C:10]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=2[CH2:18][CH2:19][C:20]([OH:22])=O)=[O:11])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH3:23][O:24][C:25]1[CH:26]=[C:27]([CH2:33][CH2:34][NH2:35])[CH:28]=[CH:29][C:30]=1[O:31][CH3:32]>>[CH3:23][O:24][C:25]1[CH:26]=[C:27]([CH2:33][CH2:34][NH:35][C:20](=[O:22])[CH2:19][CH2:18][C:13]2[CH:14]=[CH:15][CH:16]=[CH:17][C:12]=2[C:10]([NH:9][CH2:8][CH2:7][C:1]2[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=2)=[O:11])[CH:28]=[CH:29][C:30]=1[O:31][CH3:32]Participants
3
Procedure
This was prepared from the product of step (c) and 3,4-dimethoxybenzeneethanamine using the procedure of Example 6(c) mp 122°-3°.
Sources & evidence
- ORD record
- ord-cfef0f2cc3534b81a7f8b308f054f8b3
- Source dataset
- uspto-grants-1988_01
- Patent number
- US04720586
Reaction notes
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