1-(4,4-Difluorocyclohexyl)methanamine hydrochloride → HCID 178426421, compound
Reaction equation
[C:1]([C:3]1[CH:8]=[CH:7][C:6]([C:9]2[CH:10]=[N:11][N:12]([C:15]3[CH:23]=[CH:22][C:18]([C:19](O)=[O:20])=[CH:17][N:16]=3)[C:13]=2[OH:14])=[C:5]([CH3:24])[CH:4]=1)#[N:2].Cl.[F:26][C:27]1([F:35])[CH2:32][CH2:31][CH:30]([CH2:33][NH2:34])[CH2:29][CH2:28]1>>[C:1]([C:3]1[CH:8]=[CH:7][C:6]([C:9]2[CH:10]=[N:11][N:12]([C:15]3[CH:23]=[CH:22][C:18]([C:19]([NH:34][CH2:33][CH:30]4[CH2:31][CH2:32][C:27]([F:35])([F:26])[CH2:28][CH2:29]4)=[O:20])=[CH:17][N:16]=3)[C:13]=2[OH:14])=[C:5]([CH3:24])[CH:4]=1)#[N:2]Participants
3
Procedure
The title compound was prepared in a manner similar to Example 227 using 6-(4-(4-cyano-2-methylphenyl)-5-hydroxy-1H-pyrazol-1-yl)nicotinic acid and (4,4-difluorocyclohexyl)methanamine hydrochloride. 1H NMR (400 MHz, DMSO-d6) δ 1.09-1.25 (m, 2 H) 1.60-1.82 (m, 5 H) 1.95 (d, J=8.1 Hz, 2 H) 2.37 (s, 3 H) 3.15 (t, J=6.3 Hz, 2H) 7.59 (d, J=7.6 Hz, 1 H) 7.67 (s, 1 H) 8.36 (br. s., 1 H) 8.70 (br. s., 1 H) 8.82-8.88 (m, 1H) 13.16 (br. s., 1 H). MS m/z [M+H]+ 452.5.
Sources & evidence
- ORD record
- ord-8d333e1a95ac4e1d9a17a5733816c224
- Source dataset
- uspto-grants-2015_05
- Patent number
- US09040522B2
Reaction notes
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