Hydrochloric Acid → HCID 70248394, compound
Reaction equation
[C:1]1([CH2:7][CH2:8][CH2:9][N:10]2[CH2:15][CH2:14][CH:13]([C:16](=[O:31])/[CH:17]=[CH:18]/[C:19]3[S:29][C:28]4[N:30]5[C:21](=[CH:22][N:23]=[C:24]5[CH:25]=[CH:26][CH:27]=4)[CH:20]=3)[CH2:12][CH2:11]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[ClH:32]>CO>[ClH:32].[ClH:32].[C:1]1([CH2:7][CH2:8][CH2:9][N:10]2[CH2:11][CH2:12][CH:13]([C:16](=[O:31])/[CH:17]=[CH:18]/[C:19]3[S:29][C:28]4[N:30]5[C:21](=[CH:22][N:23]=[C:24]5[CH:25]=[CH:26][CH:27]=4)[CH:20]=3)[CH2:14][CH2:15]2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
In 2 ml of methanol was dissolved 0.159 g of (E)-1-[1-(3-phenylpropan-1-yl)piperidin-4-yl]-3-(5-thia-1,8b-diazaacenaphthylen-4-yl)propen-1-one, followed by addition of a stoichiometric excess of methanolic hydrochloric acid, and the mixture was stirred for 10 minutes. This reaction mixture was concentrated and crystallized from ethanol-diethyl ether to provide the title compound.
Workup
- concentrationThis reaction mixture was concentrated
- customcrystallized from ethanol-diethyl ether
Sources & evidence
- ORD record
- ord-4b073e624666499ab88da7750cc99b68
- Source dataset
- uspto-grants-2001_05
- Patent number
- US06235731B1
Reaction notes
Loading…