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| | 1-(1-Benzothiophen-4-yl)piperazine hydrochloride Basic information |
| Product Name: | 1-(1-Benzothiophen-4-yl)piperazine hydrochloride | | Synonyms: | Piperazine, 1-benzo[b]thien-4-yl-, hydrochloride;1-Benzo[b]thien-4-yl-piperazine hydrochloride;Brexpiprazole Intermediate 2;1-benzo[b]thien-4-yl-;1-benzo[b]thien-4-yl-, hydrochloride;1-Benzo[b]thien-4-ylpiperazine Monohydrochloride;1-(1-benzothiophen-4-yl)piperazine hydrochloride;7-(4-chlorobutoxy)-1-(4-chlorobutyl)quinolin-2(1H)-one | | CAS: | 913614-18-3 | | MF: | C12H15ClN2S | | MW: | 254.7789 | | EINECS: | 812-454-4 | | Product Categories: | | | Mol File: | 913614-18-3.mol |  |
| | 1-(1-Benzothiophen-4-yl)piperazine hydrochloride Chemical Properties |
| Melting point | >250°C (dec.) | | storage temp. | Keep in dark place,Sealed in dry,Room Temperature | | solubility | DMSO (Slightly, Heated), Methanol (Very Slightly) | | form | Solid | | color | White |
| | 1-(1-Benzothiophen-4-yl)piperazine hydrochloride Usage And Synthesis |
| Uses | 4-Piperazinylbenzothiophene hydrochloride is the raw material for preparing piperazine-substituted benzothiophene, which can be used for the treatment and prevention of mental diseases including central nervous system diseases. | | Synthesis | 
Synthesis of 4-(1-piperazinyl)benzo[b]thiophene hydrochloride 4-Chlorobenzo[b]thiophene (5.00 g), piperazine (5.11 g), palladium acetate (II) (2.7 mg), tri-tert-butylphosphonium tetraphenylborate (6.2 mg), sodium tert-butoxide (8.548 g), and xylene (70 ml) were stirred at 120 to 130°C for 5 hours. After the reaction mixture was cooled to room temperature, water was added thereto, and the layers were separated. The xylene layer was washed with water, and then with saline. After addition of activated carbon, the mixture was stirred at room temperature for 30 minutes. After filtration of the mixture, concentrated hydrochloric acid was added to the filtrate, and the resulting mixture was stirred at room temperature for 30 minutes. The precipitated crystals were collected by filtration and dried to obtain compound. Yield: 6.94 g. 1H-NMR (DMSO-d6) δ ppm; 3.30 (4H, br.s), 3.61 (4H, br.s), 6.97 (1H, d, J = 7.8 Hz), 7.32 (1H, br. dd, J = 8.4, 7.8 Hz), 7.53 (1H, d, J = 5.6 Hz), 7.70 (1H, d, J = 8.4 Hz), 7.76 (1H, d, J = 5.6 Hz), 9.37 (1H, br.s). |
| | 1-(1-Benzothiophen-4-yl)piperazine hydrochloride Preparation Products And Raw materials |
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