1-[3-(Trifluoromethyl)pyridin-2-yl]piperazine → (RS)-1-Benzenesulfonyl-3-cyclohexyl-4-[4-(3-trifluoromethyl-pyridin-2-yl)-piperazine-1-carbonyl]-imidazolidin-2-one
Reaction equation
[C:1]1([S:7]([N:10]2[CH2:14][CH:13]([C:15]([OH:17])=O)[N:12]([CH:18]3[CH2:23][CH2:22][CH2:21][CH2:20][CH2:19]3)[C:11]2=[O:24])(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[F:25][C:26]([F:40])([F:39])[C:27]1[C:28]([N:33]2[CH2:38][CH2:37][NH:36][CH2:35][CH2:34]2)=[N:29][CH:30]=[CH:31][CH:32]=1>>[C:1]1([S:7]([N:10]2[CH2:14][CH:13]([C:15]([N:36]3[CH2:37][CH2:38][N:33]([C:28]4[C:27]([C:26]([F:40])([F:25])[F:39])=[CH:32][CH:31]=[CH:30][N:29]=4)[CH2:34][CH2:35]3)=[O:17])[N:12]([CH:18]3[CH2:23][CH2:22][CH2:21][CH2:20][CH2:19]3)[C:11]2=[O:24])(=[O:9])=[O:8])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1Participants
3
Procedure
In analogy to example 1, (RS)-1-benzenesulfonyl-3-cyclohexyl-2-oxo-imidazolidine-4-carboxylic acid was coupled with 1-[3-(trifluoromethyl)pyrid-2-yl]piperazine to give the title compound as a colorless solid. MS: 565.8 ([M+H]+)
Sources & evidence
- ORD record
- ord-a25891797bec459e92bfeddb0cf05072
- Source dataset
- uspto-grants-2009_12
- Patent number
- US07625902B2
Reaction notes
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