Hydrochloric Acid → HCID 67519603, compound
Reaction equation
[CH3:1][N: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)=[CH:5][C:4]([CH3:34])=[N:3]1.[ClH:35]>C(OCC)C>[ClH:35].[CH3:1][N: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:29])([F:30])[F:31])=[CH:24][CH:23]=5)([CH2:19]4)[CH2:17]3)[CH:12]=2)=[CH:5][C:4]([CH3:34])=[N:3]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
5-(1,3-dimethyl-1H-pyrazol-5-yl)-1-(3-{(1S,5R)-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hex-3-yl}propyl)-2,4(1H,3H)-pyrimidinedione (E3, 90 mg, 0.177 mmol) was dissolved in diethyl ether (2 ml) and HCl 1M in diethylether (0.177 mmol, 0.177 ml) was added dropwise. The white solid obtained was triturated in Et2O (2×4 ml) to give, after filtration, the title compound (50 mg, 0.078 mmol).
Workup
- customThe white solid obtained
- customwas triturated in Et2O (2×4 ml)
- customto give
- filtrationafter filtration
Sources & evidence
- ORD record
- ord-b96b92a5f39e4ca0996654cc9a61fb6c
- Source dataset
- uspto-grants-2012_05
- Patent number
- US08178549B2
Reaction notes
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