2-Indancarboxylic Acid → HCID 70024153, compound
Reaction equation
[CH2:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3][CH:2]1[C:10]([OH:12])=O.[CH2:13]1[O:24][C:23]2[CH:22]=[C:21]3[C:17]([C:18]([C:25]4[CH2:26][CH2:27][NH:28][CH2:29][CH:30]=4)=[CH:19][NH:20]3)=[CH:16][C:15]=2[O:14]1>>[CH2:3]1[C:4]2[C:9](=[CH:8][CH:7]=[CH:6][CH:5]=2)[CH2:1][CH:2]1[C:10]([N:28]1[CH2:29][CH:30]=[C:25]([C:18]2[C:17]3[C:21](=[CH:22][C:23]4[O:24][CH2:13][O:14][C:15]=4[CH:16]=3)[NH:20][CH:19]=2)[CH2:26][CH2:27]1)=[O:12]Participants
3
Procedure
Prepared from 9a and 5,6-methylenedioxy-3-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indole.
Sources & evidence
- ORD record
- ord-b37eb764fea54819a969ff5e2bca3138
- Source dataset
- uspto-grants-2002_03
- Patent number
- US06352988B2
Reaction notes
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