Hydrochloric Acid → HCID 68431841, compound
Reaction equation
[C:1]1([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][CH: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)[N:12]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[ClH:34]>C(OCC)C>[ClH:34].[C:1]1([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:23]=[CH:24][C:25]([C:28]([F:30])([F:31])[F:29])=[CH:26][CH:27]=5)([CH2:19]4)[CH2:17]3)[N:12]=2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
6-phenyl-2-(3-{(1S)-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hex-3-yl}propyl)-1,2,4-triazine-3,5(2H,4H)-dione (9 mg 0.019 mmol) was diluted in diethyl ether (1 ml) and hydrochloric acid 1M in Et2O (0.022 ml, 0.022 mmol) under nitrogen atmosphere. Solvent was removed and the residue triturated in Et2O (2×1 mL), obtaining 3.2 mg of title compound as a white solid (27% yield).
Workup
- customSolvent was removed
- customthe residue triturated in Et2O (2×1 mL)
Sources & evidence
- ORD record
- ord-01c0ca8a0a4445239d043c19644355b8
- Source dataset
- uspto-grants-2012_07
- Patent number
- US08217168B2
Reaction notes
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