Isopropylamine → 5-[(1-Methylethyl)amino]-1-phenyl-N-tricyclo[3.3.1.13,7]dec-2-yl-1H-pyrazole-4-carboxamide
Reaction equation
[CH:1]12[CH2:10][CH:5]3[CH2:6][CH:7]([CH2:9][CH:3]([CH2:4]3)[CH:2]1[NH:11][C:12]([C:14]1[CH:15]=[N:16][N:17]([C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=3)[C:18]=1Cl)=[O:13])[CH2:8]2.[CH:26]([NH2:29])([CH3:28])[CH3:27]>>[CH:1]12[CH2:10][CH:5]3[CH2:6][CH:7]([CH2:9][CH:3]([CH2:4]3)[CH:2]1[NH:11][C:12]([C:14]1[CH:15]=[N:16][N:17]([C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=3)[C:18]=1[NH:29][CH:26]([CH3:28])[CH3:27])=[O:13])[CH2:8]2Participants
3
Procedure
5-Isopropylamino-1-phenyl-1H-pyrazole-4-carboxylic acid adamantan-2-ylamide was prepared using Procedure A from 5-chloro-1-phenyl-1H-pyrazole-4-carboxylic acid adamantan-2-ylamide (Intermediate 3) and isopropylamine. Mass spectrum (ES) MH+=379.
Sources & evidence
- ORD record
- ord-233992fb5eed4f60bddfe6a257bc8fac
- Source dataset
- uspto-grants-2010_09
- Patent number
- US07790711B2
Reaction notes
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