Identification | More | [Name]
Tiapride hydrochloride | [CAS]
51012-33-0 | [Synonyms]
N-[2-(DIETHYLAMINO)ETHYL]-5-[METHYL-SULFONYL]-O-ANISAMIDE HYDROCHLORIDE TIAPRIDE 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 Grinolart Tialaread Tiaprim Tiaryl | [EINECS(EC#)]
256-908-4 | [Molecular Formula]
C15H25ClN2O4S | [MDL Number]
MFCD00133861 | [Molecular Weight]
364.89 | [MOL File]
51012-33-0.mol |
Hazard Information | Back Directory | [Chemical Properties]
White Solid | [Originator]
Tiapridal,Delagrange,France,1977 | [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 | [storage]
Store at -20°C, protect from light |
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