Tiapride hydrochloride
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
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.
- form
- Solid
- color
- White
- Merck
- 14,9421
- CAS DataBase Reference
- 51012-33-0(CAS DataBase Reference)
MSDS
- Language:English Provider:SigmaAldrich
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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