Hydrochloric Acid → 2,4-dioxo-1-(4-{(1S,5R)-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hex-3-yl}butyl)-1,2,3,4-tetrahydro-5-pyrimidinecarbonitrile hydrochloride
Reaction equation
[O:1]=[C:2]1[NH:7][C:6](=[O:8])[C:5]([C:9]#[N:10])=[CH:4][N:3]1[CH2:11][CH2:12][CH2:13][CH2:14][N:15]1[CH2:20][C@H:19]2[C@:17]([C:21]3[CH:26]=[CH:25][C:24]([C:27]([F:30])([F:29])[F:28])=[CH:23][CH:22]=3)([CH2:18]2)[CH2:16]1.[ClH:31]>O1CCOCC1>[ClH:31].[O:1]=[C:2]1[NH:7][C:6](=[O:8])[C:5]([C:9]#[N:10])=[CH:4][N:3]1[CH2:11][CH2:12][CH2:13][CH2:14][N:15]1[CH2:20][C@H:19]2[C@:17]([C:21]3[CH:22]=[CH:23][C:24]([C:27]([F:30])([F:29])[F:28])=[CH:25][CH:26]=3)([CH2:18]2)[CH2:16]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
2,4-dioxo-1-(4-{(1S,5R)-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hex-3-yl}butyl)-1,2,3,4-tetrahydro-5-pyrimidinecarbonitrile was treated with a solution of 4N HCl in dioxane (200 μl) to give the title compound as a pale yellow solid. (76 mg).
Sources & evidence
- ORD record
- ord-6cefeec708104acc93a0cdf1c7e079f2
- Source dataset
- uspto-grants-2010_06
- Patent number
- US07727988B2
Reaction notes
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