Reaction equation
[NH2:1][C:2]1[CH:3]=[CH:4][C:5]([CH3:21])=[C:6]([C:8]2[CH:13]=[CH:12][C:11]([C:14]([NH:16][CH2:17][CH:18]3[CH2:20][CH2:19]3)=[O:15])=[CH:10][CH:9]=2)[CH:7]=1.[O:22]1[CH:26]=[CH:25][CH:24]=[C:23]1[CH2:27][C:28](O)=[O:29]>>[CH:18]1([CH2:17][NH:16][C:14]([C:11]2[CH:12]=[CH:13][C:8]([C:6]3[C:5]([CH3:21])=[CH:4][CH:3]=[C:2]([NH:1][C:28](=[O:29])[CH2:27][C:23]4[O:22][CH:26]=[CH:25][CH:24]=4)[CH:7]=3)=[CH:9][CH:10]=2)=[O:15])[CH2:20][CH2:19]1Participants
3
Procedure
N-(4′-{[(Cyclopropylmethyl)amino]carbonyl}6-methyl -1,1′-biphenyl-3-yl)-2-(fur-2-yl)acetamide was prepared from 5′-amino-N-(cyclopropylmethyl)-2′-methyl-1,1′-biphenyl-4- carboxamide and fur-2-ylacetic acid using method D. NMR; δH [2H6]—DMSO 10.17,(1H, s), 8.61,(1H, t), 7.91,(2H, d), 7.55,(1H, m), 7.50-7.48,(2H, m), 7.40,(2H, d), 7.23,(1H, d), 6.38,(1H, m), 6.25,(1H, d), 3.70,(2H, s), 3.16,(2H, t), 2.16,(3H, s), 1.04,(2H, m), 0.42,(2H, m). LCMS: retention time 3.26 min, MH+389.
Sources & evidence
- ORD record
- ord-5fe580bfd24741fba4ffe7a35292f54a
- Source dataset
- uspto-grants-2008_10
- Patent number
- US07432289B2
Linked notes
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