Hydrochloric Acid → HCID 67307357, compound
Reaction equation
[ClH:1].CCOCC.[CH3:7][O:8][C:9]1[CH:10]=[C:11]2[C:16](=[CH:17][CH:18]=1)[C:15]([O:19][C:20]1[CH:25]=[CH:24][C:23]([O:26][CH2:27][CH2:28][N:29]3[CH2:34][CH2:33][CH2:32][CH2:31][CH2:30]3)=[CH:22][CH:21]=1)=[C:14]([C:35]1[C:36]([C:40]#[N:41])=[CH:37][S:38][CH:39]=1)[CH:13]=[CH:12]2>ClCCl>[ClH:1].[CH3:7][O:8][C:9]1[CH:10]=[C:11]2[C:16](=[CH:17][CH:18]=1)[C:15]([O:19][C:20]1[CH:21]=[CH:22][C:23]([O:26][CH2:27][CH2:28][N:29]3[CH2:34][CH2:33][CH2:32][CH2:31][CH2:30]3)=[CH:24][CH:25]=1)=[C:14]([C:35]1[C:36]([C:40]#[N:41])=[CH:37][S:38][CH:39]=1)[CH:13]=[CH:12]2Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Add a solution of Hydrogen Chloride in ether (1 M, 180 μL, 180.0 μmol) to a prepared solution of 4-(6-methoxy-1-(4-(2-(piperidin-1-yl)ethoxy)phenoxy)naphthalen-2-yl)thiophene-3-carbonitrile (87 mg, 179.5 μmol) in Dichloromethane (2 mL). Stir the mixture for 10 min. Concentrate the mixture to obtain the title compound (95 mg, 179 μmol).
Workup
- concentrationConcentrate the mixture
Sources & evidence
- ORD record
- ord-9802a598567e4531b4aea992a811f9b2
- Source dataset
- uspto-grants-2013_07
- Patent number
- US08476300B2
Reaction notes
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