HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(4-chlorobutyl)-3,4-dihydroquinolin-2(1H)-one → 1-[4-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)butyl]-3,4-dihydro-1H-quinolin-2-one hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(4-chlorobutyl)-3,4-dihydroquinolin-2(1H)-one | HCID 20469712 | — |
| Reactant | Ethanol hydrochloride | HCID 21887872 | — |
| Reactant | 1-[4-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)butyl]-3,4-dihydro-1H-quinolin-2-one | HCID 66884891 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-[4-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)butyl]-3,4-dihydro-1H-quinolin-2-one hydrochloride | HCID 66884890 | — |
Reaction Steps
By a similar method as in Example 1, 1-[4-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)butyl]-3,4-dihydro-1H-quinolin-2-one was prepared from 1-(4-chlorobutyl)-3,4-dihydro-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-[4-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)butyl]-3,4-dihydro-1H-quinolin-2-one hydrochloride was obtained in the form of a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09206167B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-2952a5820e694cff8b22074059f952aa |
| Source note | uspto-grants-2015_12 |