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Tiapride hydrochloride

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Tiapride hydrochloride Basic information

Product Name:
Tiapride hydrochloride
Synonyms:
  • N-[2-(DIETHYLAMINO)ETHYL]-5-[METHYL-SULFONYL]-O-ANISAMIDE HYDROCHLORIDE
  • n-(2-(diethylamino)ethyl)-2-methoxy-5-(methylsulfonyl)benzamidehydrochloride
  • n-(2-(diethylamino)ethyl)-2-methoxy-5-(methylsulfonyl)-benzamidmonohydroch
  • n-(2-(diethylamino)ethyl)-2-methoxy-5-(methylsulfonyl)-benzamidmonohydrochloride
  • N-[2-(diethylamino)ethyl]-2-methoxy-5-(methylsulphonyl)benzamide monohydrochloride
  • TiapridHCl
  • Tiapridhydrochlorid
  • Cuckool
CAS:
51012-33-0
MF:
C15H25ClN2O4S
MW:
364.89
EINECS:
256-908-4
Mol File:
51012-33-0.mol
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Tiapride hydrochloride Chemical Properties

Melting point:
approximate 200℃ (dec.)
storage temp. 
2-8°C
solubility 
Very soluble in water, soluble in methanol, slightly soluble in anhydrous ethanol.
color 
White
Merck 
14,9421
CAS DataBase Reference
51012-33-0(CAS DataBase Reference)
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Safety Information

WGK Germany 
2
RTECS 
CV4203800
HS Code 
2930.90.2900

MSDS

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Tiapride hydrochloride Usage And Synthesis

Chemical Properties

White Solid

Originator

Tiapridal,Delagrange,France,1977

Uses

Tiapride is a D2 and D3 dopamine receptor antagonist and a antipsychotic drug predominately used in the pharmacotherapy of patients with dementia.

Uses

Dopamine antagonist;Antidyskinetic

Uses

Tiapride hydrochloride is a D2 and D3 dopamine receptor antagonist and a antipsychotic drug predominately used in the pharmacotherapy of patients with dementia.

Definition

ChEBI: Tiapride hydrochloride is a member of benzamides.

Manufacturing Process

5 g of 2-methoxy-5-methylsulfonylbenzoic acid, 50 ml of dioxan, 3.02 ml of triethylamine and 3 g of isobutyl chloroformate were introduced into a 250 ml balloon flask at ambient temperature.
After the mixture had been stirred for 30 minutes, 3 g of N,N_x0002_diethylethylenediamine were added. The reaction mixture was stirred for 6 hours and the solvents were evaporated under vacuum.
The residue was dissolved in 50 ml of water and the solution was made alkaline with sodium hydroxide. The precipitate formed was filtered, washed and dried in a drying oven at 60°C. 6 g of N-(diethylaminoethyl)-2-methoxy- 5-methylsulfonylbenzamide (melting point: 124°C to 125°C) was produced.

Therapeutic Function

Antiemetic

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