Benzylamine → N-Benzyl 4-hydroxy-1-methyl-1H-indole-2-carboxamide
Reaction equation
C([O:8][C:9]1[CH:17]=[CH:16][CH:15]=[C:14]2[C:10]=1[CH:11]=[C:12]([C:19]([OH:21])=O)[N:13]2[CH3:18])C1C=CC=CC=1.[CH2:22]([NH2:29])[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1>>[CH2:22]([NH:29][C:19]([C:12]1[N:13]([CH3:18])[C:14]2[C:10]([CH:11]=1)=[C:9]([OH:8])[CH:17]=[CH:16][CH:15]=2)=[O:21])[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1Participants
3
Procedure
From 4-benzyloxy-1-methyl-1H-indole-2-carboxylic acid and benzylamine the title compound was prepared by a method analogous to that described in Example 11. MS ES (M++H)=281.
Sources & evidence
- ORD record
- ord-28656a1d93a345fa99a500ff83ea419e
- Source dataset
- uspto-grants-2008_07
- Patent number
- US07402604B2
Reaction notes
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