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ChemicalBook--->CAS DataBase List--->57775-22-1

57775-22-1

57775-22-1 Structure

57775-22-1 Structure
IdentificationBack Directory
[Name]

2-[3-[4-(3-chlorophenyl)piperazin-1-yl]propyl]-4,5-diethyl-2,4-dihydro-3H-1,2,4-triazol-3-one monohydrochloride
[Synonyms]

Staff
Etonin
Etoran
ST-1191
Axiomin
Tropene
Depracer
Deprecer
NSC304398
NSC-304398
NSC 304398
MCN-A-2673-11
Trazodone Impurity 48
Trazodone Impurity 53
2-[3-[4-(3-Chlorophenyl)-1-piperazinyl]propyl]-4,5-diethyl-2,4-dihydro-3H-1,2,4-triazol-3-one Hydrochloride
2-[3-[4-(3-chlorophenyl)piperazin-1-yl]propyl]-4,5-diethyl-2,4-dihydro-3H-1,2,4-triazol-3-one monohydrochloride
2-[3-[4-(3-Chlorophenyl)-1-piperazinyl]propyl]-4,5-diethyl-2,4-dihydro-3H-1,2,4-triazol-3-one monohydrochloride
[Molecular Formula]

C19H29Cl2N5O
[Molecular Weight]

414.372
Safety DataBack Directory
[Toxicity]

LD50 in mice, rats (mg/kg): 580, 720 orally; 72, 62 i.v.; 135, 120 i.p. (Lisciani)
Hazard InformationBack Directory
[Manufacturing Process]

(a). 3,4-Diethyl-δ2-1,2,4-triazolin-5-one (62 g) is dissolved in anhydrous dioxane (about 500 ml) and NaH (21 g) in a 50 percent oily suspension is added. The solution is heated for 30 min under reflux and NmetachlorophenyI- N'-(3-chloro-n-propyl)piperazine (119 g) is added under stirring. The solution is heated for 20 hours under reflux. The solvent is then eliminated under reduced pressure and the residue is treated with 2 N HCl. The solution is washed with ether so as to eliminate the oil present in the hydride solution, and made alkaline with 50% K2CO3. It is extracted with ether and dried, the solvent is eliminated and the residue is distilled under reduced pressure. 115 g of 2-(3-(4-(3-chlorophenyl)-1-piperazinyl)propyl)- 4,5-diethyl-2,4-dihydro-1,2,4-triazol-3-one are obtained. B.P. 230°C/0.5 mm.
2-(3-(4-(3-Chlorophenyl)-1-piperazinyl)propyl)-4,5-diethyl-2,4-dihydro-1,2,4- triazol-3-one hydrochloride was prepared by standard procedures, melting point 197-198°C (recrystallization from isopropanol).
(b). 3,4-Diethyl-δ2-1,2,4-triazolin-5-one (1 g) and 3-bromo-1-chloropropane (6.6 g) are added to a solution of Na (0.98 g) in methanol (20 ml). The solution is refluxed until the pH becomes neutral, poured into water, extracted with ether. The solvent is eliminated and the residual oil is distilled. 1-(3- Chloropropyl)-3,4-diethyl-δ2-1,2,4-triazolin-5-one boils at 121°C/0.05 mm.
1-(3-Chloropropyl)-3,4-diethyl-δ2-1,2,4-triazolin-5-one (1.0 g), NmetachlorophenyIpiperazine (0.9 g) and triethylamine (0.46 g) in toluene (25 ml) are refluxed for 12 hours. The solution is treated with 5 N NaOH, extracted with ether and steam-distilled. The residue is extracted with ether and the ethereal solution is treated with ethereal HCl. 2-(3-(4-(3- Chlorophenyl)-1-piperazinyl)propyl)-4,5-diethyl-2,4-dihydro-1,2,4-triazol-3- one hydrochloride has melting point 197-198°C (recrystallization from isopropanol).
[Therapeutic Function]

Antidepressant, Anxiolytic
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