o-Phenylbenzoic acid → HCID 24964111, compound
Reaction equation
[NH:1]1[CH2:6][CH2:5][CH2:4][C@@H:3]([NH:7][C:8]([C:10]2[CH:11]=[CH:12][CH:13]=[C:14]3[O:18][CH:17]=[CH:16][C:15]=23)=[O:9])[CH2:2]1.[C:19]1([C:28]2[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=2)[C:20]([C:25](O)=[O:26])=[CH:21][CH:22]=[CH:23][CH:24]=1>>[C:19]1([C:28]2[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=2)[C:20]([C:25]([N:1]2[CH2:6][CH2:5][CH2:4][C@@H:3]([NH:7][C:8]([C:10]3[CH:11]=[CH:12][CH:13]=[C:14]4[O:18][CH:17]=[CH:16][C:15]=34)=[O:9])[CH2:2]2)=[O:26])=[CH:21][CH:22]=[CH:23][CH:24]=1Participants
3
Procedure
prepared by reaction of (R)-benzofuran-4-carboxylic acid piperidin-3-ylamide with biphenyl-2-carboxylic acid acid.
Sources & evidence
- ORD record
- ord-d7d22f4d11ab4f428c7dbe9b5459a731
- Source dataset
- uspto-grants-2012_03
- Patent number
- US08133901B2
Reaction notes
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