Ethanol hydrochloride → HCID 66884873, 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][CH2:20][N:21]4[C:30]5[C:25](=[CH:26][CH:27]=[CH:28][CH:29]=5)[CH:24]=[CH:23][C:22]4=[O:31])[CH2:12][CH2:11]3)=[CH:7][CH:8]=[CH:9][C:2]1=2.[Cl:32]CCCCCN1C2C(=CC=CC=2)C=CC1=O.C(O)C.Cl>C(O)C>[ClH:32].[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][CH2:20][N:21]4[C:30]5[C:25](=[CH:26][CH:27]=[CH:28][CH:29]=5)[CH:24]=[CH:23][C:22]4=[O:31])[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, 1-[5-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)pentyl]-1H-quinolin-2-one was prepared from 1-(5-chloropentyl)-1H-quinolin-2-one, and after it was made into an ethanol solution, 1N hydrochloric acid ethanol solution was added thereto, precipitated crystals were separated by filtration, and thereby 1-[5-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)pentyl]-1H-quinolin-2-one hydrochloride was obtained in the form of a white powder.
Workup
- additionwas added
- customprecipitated crystals
- customwere separated by filtration
Sources & evidence
- ORD record
- ord-df390235c0c34cc5a5ddff4f6182a57e
- Source dataset
- uspto-grants-2013_01
- Patent number
- US08349840B2
Reaction notes
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