Cyclopentylamine → HCID 71075244, compound
Reaction equation
[CH:1]1([NH2:6])[CH2:5][CH2:4][CH2:3][CH2:2]1.C([O:11][C:12]([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=1[C:20]1[CH:25]=[CH:24][C:23]([CH2:26][N:27]2[C:35]3[C:30](=[CH:31][C:32]([C:36](O)=[O:37])=[CH:33][CH:34]=3)[C:29]([CH3:39])=[C:28]2[CH3:40])=[CH:22][CH:21]=1)=[O:13])(C)(C)C>>[CH:1]1([NH:6][C:36]([C:32]2[CH:31]=[C:30]3[C:35](=[CH:34][CH:33]=2)[N:27]([CH2:26][C:23]2[CH:22]=[CH:21][C:20]([C:15]4[C:14]([C:12]([OH:13])=[O:11])=[CH:19][CH:18]=[CH:17][CH:16]=4)=[CH:25][CH:24]=2)[C:28]([CH3:40])=[C:29]3[CH3:39])=[O:37])[CH2:5][CH2:4][CH2:3][CH2:2]1Participants
3
Procedure
The title compound was prepared following the same general protocol as described in Steps 8-9, Example 1, using cyclopentylamine and 1-((2′-(tert-butoxycarbonyl)biphenyl-4-yl)methyl)-2,3-dimethyl-1H-indole-5-carboxylic acid.
Sources & evidence
- ORD record
- ord-febf92fa766d4f89b11064560a4a046a
- Source dataset
- uspto-grants-2015_02
- Patent number
- US08957093B2
Reaction notes
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