HCID 69717260, compound → HCID 131723260, compound
Reaction equation
[CH2:1]([NH:5][C:6]([C@@H:8]1[C@H:16]([CH3:17])[C:15]2[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=2)[N:9]1[C:18](=[O:23])[C@@H:19]([NH2:22])[CH2:20][CH3:21])=[O:7])[CH2:2][CH2:3][CH3:4].[CH2:24](NC([C@H]1[C@@H](C)C2C(=CC=CC=2)N1C(=O)[C@@H](N)CC)=O)CCC>>[CH2:1]([NH:5][C:6]([CH:8]1[C:16]([CH3:24])([CH3:17])[C:15]2[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=2)[N:9]1[C:18](=[O:23])[C@@H:19]([NH2:22])[CH2:20][CH3:21])=[O:7])[CH2:2][CH2:3][CH3:4]Participants
3
Procedure
1-(2(S)-aminobutyryl)-3(R)-methylindoline-2(S)-carboxylic acid butylamide and 1-(2(S)-aminobutyryl)-3(S)-methylindoline-2(R)-carboxylic acid butylamide;
Sources & evidence
- ORD record
- ord-27974d8763d94d6781f65f3b2e40d17f
- Source dataset
- uspto-grants-2002_06
- Patent number
- US06403561B1
Reaction notes
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