(+-)-alpha-Methyltryptamine → 2-Methyl-1,2,3,6-tetrahydroazepino[4,5-b]indole-5-carboxylic acid n-propyl ester
Reaction equation
[CH3:1][CH:2]([CH2:4][C:5]1[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[NH:7][CH:6]=1)[NH2:3].Br[CH2:15][C:16](=O)[C:17]([O:19][CH2:20][CH2:21][CH3:22])=[O:18]>>[CH2:20]([O:19][C:17]([C:16]1[C:6]2[NH:7][C:8]3[CH:9]=[CH:10][CH:11]=[CH:12][C:13]=3[C:5]=2[CH2:4][CH:2]([CH3:1])[NH:3][CH:15]=1)=[O:18])[CH2:21][CH3:22]Participants
3
Procedure
2-Methyl-1,2,3,6-tetrahydroazepino[4,5-b]indole-5-carboxylic acid n-propyl ester was prepared in the manner described in Example 1A using α-methyl tryptamine and n-propyl 3-bromopyruvate; MS (ESI): 285 (MH+).
Sources & evidence
- ORD record
- ord-dbe97157262842f5b2b6c5e43f8dfc1d
- Source dataset
- uspto-grants-2009_02
- Patent number
- US07485634B2
Reaction notes
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