Hydrochloric Acid → 6-Methoxy-1-(4-(2-(piperidin-1-yl)ethoxy)phenoxy)naphthalen-2-yl trifluoromethanesulfonate hydrochloride
Reaction equation
[ClH:1].CCOCC.[F:7][C:8]([F:42])([F:41])[S:9]([O:12][C:13]1[CH:22]=[CH:21][C:20]2[C:15](=[CH:16][CH:17]=[C:18]([O:23][CH3:24])[CH:19]=2)[C:14]=1[O:25][C:26]1[CH:31]=[CH:30][C:29]([O:32][CH2:33][CH2:34][N:35]2[CH2:40][CH2:39][CH2:38][CH2:37][CH2:36]2)=[CH:28][CH:27]=1)(=[O:11])=[O:10]>ClCCl>[ClH:1].[F:41][C:8]([F:7])([F:42])[S:9]([O:12][C:13]1[CH:22]=[CH:21][C:20]2[C:15](=[CH:16][CH:17]=[C:18]([O:23][CH3:24])[CH:19]=2)[C:14]=1[O:25][C:26]1[CH:27]=[CH:28][C:29]([O:32][CH2:33][CH2:34][N:35]2[CH2:36][CH2:37][CH2:38][CH2:39][CH2:40]2)=[CH:30][CH:31]=1)(=[O:11])=[O:10]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Add a solution of hydrogen chloride in ether (1.0 M, 5.5 mL, 5.50 mmol) to a solution of 6-methoxy-1-(4-(2-(piperidin-1-yl)ethoxy)phenoxy)naphthalen-2-yl trifluoromethanesulfonate (2.62 g, 4.99 mmol) and dichloromethane (20 mL). Stir the mixture for 10 minutes and then concentrate to obtain the title compound (2.8 g, 4.99 mmol).
Workup
- concentrationconcentrate
Sources & evidence
- ORD record
- ord-00d2568438534ef0aee1e8942b66a26d
- Source dataset
- uspto-grants-2013_07
- Patent number
- US08476300B2
Reaction notes
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