2-(3,5-Bis(trifluoromethyl)phenyl)propanoic acid → (RS)-alpha-Methyl-N-[1-(3-Fluorophenyl)-4-oxocyclohexyl]-3,5-bis(trifluoromethyl)benzeneacetamide
Reaction equation
[CH3:1][CH:2]([C:6]1[CH:11]=[C:10]([C:12]([F:15])([F:14])[F:13])[CH:9]=[C:8]([C:16]([F:19])([F:18])[F:17])[CH:7]=1)[C:3](O)=[O:4].Cl.[F:21][C:22]1[CH:23]=[C:24]([C:28]2([NH2:35])[CH2:33][CH2:32][C:31](=[O:34])[CH2:30][CH2:29]2)[CH:25]=[CH:26][CH:27]=1>>[CH3:1][CH:2]([C:6]1[CH:11]=[C:10]([C:12]([F:13])([F:15])[F:14])[CH:9]=[C:8]([C:16]([F:17])([F:18])[F:19])[CH:7]=1)[C:3]([NH:35][C:28]1([C:24]2[CH:25]=[CH:26][CH:27]=[C:22]([F:21])[CH:23]=2)[CH2:29][CH2:30][C:31](=[O:34])[CH2:32][CH2:33]1)=[O:4]Participants
3
Procedure
Prepared from (RS)-α-methyl-3,5-bis(trifluoromethyl)benzeneacetic acid (Description 4) and 1-(3-fluorophenyl)-4-oxocyclohexylamine hydrochloride (Description 181) according to the method of Example 1. 1H NMR (360 MHz, CDCl3) δ 7.81 (1H, s), 7.73 (2H, s), 7.29–7.24 (1H, m), 7.06–7.03 (1H, m), 6.97–6.94 (2H, m), 5.78 (1H, s), 3.72 (1H, q, J 7.0 Hz), 2.81–2.75 (1H, m), 2.63–2.57 (1×, m), 2.44–2.24 (6H, m), and 1.53 (3H, d, J 7.0 Hz).
Sources & evidence
- ORD record
- ord-d65e50aed32e445aa577f549a75570ef
- Source dataset
- uspto-grants-2006_09
- Patent number
- US07105507B2
Reaction notes
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