Hydrochloric Acid → 6-Methoxy-1-(4-(2-(piperidin-1-yl)ethoxy)phenoxy)naphthalen-2-yl trifluoromethanesulfonate hydrochloride

HRID 445217Notes

Reaction equation

HRID 445217 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

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

  1. concentrationconcentrate

Sources & evidence

ORD record
ord-00d2568438534ef0aee1e8942b66a26d
Source dataset
uspto-grants-2013_07
Patent number
US08476300B2

Reaction notes

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