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1-(1-Benzothiophen-4-yl)piperazine hydrochloride

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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
Mol File:
913614-18-3.mol
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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
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Safety Information

HS Code 
2934999090
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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).

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