HCID 10421686, compound → HCID 66885600, compound
Reaction equation
[S:1]1[CH:5]=[CH:4][C:3]2[C:6]([N:10]3[CH2:15][CH2:14][N:13]([CH2:16][CH2:17][CH2:18][CH2:19][N:20]4[CH2:29][CH2:28][C:27]5[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=5)[C:21]4=[O:30])[CH2:12][CH2:11]3)=[CH:7][CH:8]=[CH:9][C:2]1=2.[Cl:31]CCCCN1CCC2C(=CC=CC=2)C1=O.C(O)C.Cl>C(O)C>[ClH:31].[S:1]1[CH:5]=[CH:4][C:3]2[C:6]([N:10]3[CH2:15][CH2:14][N:13]([CH2:16][CH2:17][CH2:18][CH2:19][N:20]4[CH2:29][CH2:28][C:27]5[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=5)[C:21]4=[O:30])[CH2:12][CH2:11]3)=[CH:7][CH:8]=[CH:9][C:2]1=2Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
By a similar method as in Example 1, 2-[4-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)butyl]-3,4-dihydro-2H-isoquinolin-1-one was prepared from 2-(4-chlorobutyl)-3,4-dihydro-2H-isoquinolin-1-one, and after it was made into an ethanol solution, 1N hydrochloric acid ethanol solution was added thereto, precipitated crystals were separated by filtration, recrystallized from a mixed solvent of isopropyl alcohol-ethanol and thereby 2-[4-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)butyl]-3,4-dihydro-2H-isoquinolin-1-one hydrochloride was obtained.
Workup
- additionwas added
- customprecipitated crystals
- customwere separated by filtration
- customrecrystallized from a mixed solvent of isopropyl alcohol-ethanol
Sources & evidence
- ORD record
- ord-b754c8dbd5284ca2a3f486a3885c7ec9
- Source dataset
- uspto-grants-2015_12
- Patent number
- US09206167B2
Reaction notes
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