2-Furancarboxylic acid → HCID 44578458, compound
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[C:27](O)=[O:28]>>[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:27]([C:23]4[O:22][CH:26]=[CH:25][CH:24]=4)=[O:28])[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-furamide was prepared from 5′-amino-N-(cyclopropylmethyl)-2′-methyl-1,1′-biphenyl-4-carboxamide and 2-furoic acid using method D. NMR; δH [2H6]—DMSO 10.18,(1H, s), 8.62,(1H, t), 7.93-7.91,(3H, m), 7.69,(1H, dd), 7.65,(1H, d), 7.44,(2H, d), 7.31,(1H, d), 7.27,(1H, d), 6.69,(1H, m), 3.16,(2H, m), 2.19,(3H, s), 1.04,(1H, m), 0.43,(2H, m), 0.24,(2H, m). LCMS: retention time 3.25 min, MH+375.
Sources & evidence
- ORD record
- ord-966843953051418c9b6f055a9ec498df
- Source dataset
- uspto-grants-2008_10
- Patent number
- US07432289B2
Reaction notes
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