Butylamine → HCID 131723079, compound
Reaction equation
[C:1]([O:5][C:6]([NH:8][C@@H:9]([CH2:32][CH3:33])[C:10]([N:12]1[C:20]2[C:15](=[CH:16][C:17]([O:21][CH2:22][C:23]3[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=3)=[CH:18][CH:19]=2)[CH2:14][CH:13]1[C:29]([OH:31])=O)=[O:11])=[O:7])([CH3:4])([CH3:3])[CH3:2].[CH2:34]([NH2:38])[CH2:35][CH2:36][CH3:37]>>[CH2:34]([NH:38][C:29]([CH:13]1[CH2:14][C:15]2[C:20](=[CH:19][CH:18]=[C:17]([O:21][CH2:22][C:23]3[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=3)[CH:16]=2)[N:12]1[C:10](=[O:11])[C@@H:9]([NH:8][C:6]([O:5][C:1]([CH3:2])([CH3:3])[CH3:4])=[O:7])[CH2:32][CH3:33])=[O:31])[CH2:35][CH2:36][CH3:37]Participants
3
Procedure
This compound was prepared from 1-(N-t-butoxycarbonyl-2(S)-aminobutyryl)-5-benzyloxyindoline-2-(R/S)-carboxylic acid and butyl amine as described in Example 6.
Sources & evidence
- ORD record
- ord-55413a91d7d648279308abfbfea929aa
- Source dataset
- uspto-grants-2002_01
- Patent number
- US06335360B1
Reaction notes
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