Reaction equation
N[C@@H:2]([CH2:6][C:7]1[C:15]2[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=2)[NH:9][CH:8]=1)[C:3]([OH:5])=O.[CH:16]1([NH:23][C:24]([NH2:26])=[S:25])[CH2:22][CH2:21][CH2:20][CH2:19][CH2:18][CH2:17]1>>[CH:16]1([NH:23][C:24]2[S:25][CH:2]([CH2:6][C:7]3[C:15]4[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=4)[NH:9][CH:8]=3)[C:3](=[O:5])[N:26]=2)[CH2:22][CH2:21][CH2:20][CH2:19][CH2:18][CH2:17]1Participants
3
Procedure
Synthesis was performed from (2S)-2-amino-3-(1H-indol-3-yl)propanoic acid and N-cycloheptylthiourea according to Method E and C.
Workup
- customSynthesis
Sources & evidence
- ORD record
- ord-55e3372f8d4f4f12885fdd0281818d42
- Source dataset
- uspto-grants-2013_09
- Patent number
- US08541592B2
Linked notes
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