5-Chloro-1H-indole-2-carboxylic acid → HCID 21710873, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][C:6]([C:11]([OH:13])=O)=[CH:5]2.[CH3:14][O:15][C:16](=[O:27])[C@H:17]([CH:19]([CH3:26])[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)[NH2:18]>>[Cl:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][C:6]([C:11]([NH:18][CH:17]([CH:19]([C:20]1[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=1)[CH3:26])[C:16]([O:15][CH3:14])=[O:27])=[O:13])=[CH:5]2Participants
3
Procedure
From 5-chloro-1H-indole-2-carboxylic acid and DL-β-methylphenylalanine methyl ester. mp 135-136° C.
Sources & evidence
- ORD record
- ord-192470c8da12410ea898563cfe868537
- Source dataset
- uspto-grants-2000_08
- Patent number
- US06107329
Reaction notes
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