Hydrochloric Acid → HCID 67519706, compound
Reaction equation
[CH3:1][C:2]1[C:6]([C:7]2[C:8](=[O:33])[NH:9][C:10](=[O:32])[N:11]([CH2:13][CH2:14][CH2:15][N:16]3[CH2:21][C@H:20]4[C@:18]([C:22]5[CH:27]=[CH:26][C:25]([C:28]([F:31])([F:30])[F:29])=[CH:24][CH:23]=5)([CH2:19]4)[CH2:17]3)[CH:12]=2)=[C:5]([CH3:34])[O:4][N:3]=1.[ClH:35]>O1CCOCC1>[ClH:35].[CH3:1][C:2]1[C:6]([C:7]2[C:8](=[O:33])[NH:9][C:10](=[O:32])[N:11]([CH2:13][CH2:14][CH2:15][N:16]3[CH2:21][C@H:20]4[C@:18]([C:22]5[CH:27]=[CH:26][C:25]([C:28]([F:31])([F:30])[F:29])=[CH:24][CH:23]=5)([CH2:19]4)[CH2:17]3)[CH:12]=2)=[C:5]([CH3:34])[O:4][N:3]=1Participants
4
Procedure
5-(3,5-dimethyl-4-isoxazolyl)-1-(3-{(1S,5R)-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hex-3-yl}propyl)-2,4(1H,3H)-pyrimidinedione was treated with a solution of 4N HCl in dioxane (500 μl) to give the title compound as a white solid.
Sources & evidence
- ORD record
- ord-efe0c6d0bf7749698b9246fbf7b93084
- Source dataset
- uspto-grants-2010_06
- Patent number
- US07727988B2
Reaction notes
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