HCID 71074541, compound → HCID 53389234, compound
Reaction equation
[CH:1]([C:4]1[CH:5]=[C:6]([C@@H:10]([NH2:15])[CH2:11][CH2:12][CH2:13][CH3:14])[CH:7]=[CH:8][CH:9]=1)([CH3:3])[CH3:2].C([O:20][C:21]([C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][C:24]=1[C:29]1[CH:34]=[CH:33][C:32]([CH2:35][N:36]2[C:44]3[C:39](=[CH:40][C:41]([C:45](O)=[O:46])=[CH:42][CH:43]=3)[C:38]([CH3:48])=[C:37]2[CH3:49])=[CH:31][CH:30]=1)=[O:22])(C)(C)C>>[CH:1]([C:4]1[CH:5]=[C:6]([C@@H:10]([NH:15][C:45]([C:41]2[CH:40]=[C:39]3[C:44](=[CH:43][CH:42]=2)[N:36]([CH2:35][C:32]2[CH:31]=[CH:30][C:29]([C:24]4[C:23]([C:21]([OH:22])=[O:20])=[CH:28][CH:27]=[CH:26][CH:25]=4)=[CH:34][CH:33]=2)[C:37]([CH3:49])=[C:38]3[CH3:48])=[O:46])[CH2:11][CH2:12][CH2:13][CH3:14])[CH:7]=[CH:8][CH:9]=1)([CH3:3])[CH3:2]Participants
3
Procedure
The title compound was prepared following the same general protocol as described in Step 8-9, Example 1, using the (S)-1-(3-isopropylphenyl)pentan-1-amine and the 1-((2′-(tert-butoxycarbonyl)-[1,1′-biphenyl]-4-yl)methyl)-2,3-dimethyl-1H-indole-5-carboxylic acid. ESI-MS (m/z): 587 [M+H]+.
Sources & evidence
- ORD record
- ord-861e2b0e869d4f318293cc966df009a2
- Source dataset
- uspto-grants-2015_02
- Patent number
- US08957093B2
Reaction notes
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