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2622-30-2

2622-30-2 Structure

2622-30-2 Structure
IdentificationBack Directory
[Name]

carfenazine
[CAS]

2622-30-2
[Synonyms]

Carfenazina
carfenazine
Carphenazine
Carfenazinum
Unii-cly16Y8Z7e
Einecs 220-072-9
Carfenazinum [inn-latin]
Carfenazina [inn-spanish]
1-(10-(3-(4-(2-Hydroxyethyl)-1-piperazinyl)propyl)phenothiazin-2-yl)-1-propanone
1-Propanone, 1-[10-[3-[4-(2-hydroxyethyl)-1-piperazinyl]propyl]phenoth iazin-2-yl]-
1-(10-(3-(4-(2-hydroxyethyl)piperazin-1-yl)propyl)-10H-phenothiazin-2-yl)propan-1-one
1-[10-[3-[4-(2-Hydroxyethyl)-1-piperazinyl]propyl]-10H-phenothiazin-2-yl]-1-propanone
1-Propanone,1-[10-[3-[4-(2-hydroxyethyl)-1-piperazinyl]propyl]-10H-phenothiazin-2-yl]-
[EINECS(EC#)]

220-072-9
[Molecular Formula]

C24H31N3O2S
[MOL File]

2622-30-2.mol
[Molecular Weight]

425.59
Chemical PropertiesBack Directory
[Boiling point ]

616.9±55.0 °C(Predicted)
[density ]

1.187±0.06 g/cm3(Predicted)
[storage temp. ]

Refrigerator
[solubility ]

DMSO (Slightly), Methanol (Slightly, Sonicated)
[form ]

Gel
[pka]

14.96±0.10(Predicted)
[color ]

Yellow to Orange
Hazard InformationBack Directory
[Originator]

Proketazine,Wyeth,US,1962
[Uses]

Antipsychotic.
[Uses]

Carphenazine is used as an antipsychotic.
[Manufacturing Process]

As described in US Patent 3,023,146, in a round-bottomed flask were placed 35 g of 2-propionyl phenothiazine (0.14 mol) 7 g of 50% sodium hydride in mineral oil (0.14 mol), and 240 cc of dimethyl formamide dried over sodium hydride. The resultant solution was stirred at room temperature for 2 hours, and then 88 g (0.56 mol) of trimethylene chlorobromide was added at once.
The mixture was stirred for 2 hours, heated at 60 to 70°C for 1 hour and poured into 2 liters of H2O. The resulting suspension was extracted with ether, the ether layer separated and the ether removed under vacuum. A gummy mass remained which was dissolved in decalin and the solution was partly distilled to remove excess chlorobromide. After removal of most of the decalin under vacuum, the residue was treated with a large excess of N-(β- hydroxyethyl)-piperazine and heated on a steam bath for 2 hours. This material was extracted with dilute aqueous HCl, this acid layer neutralized with aqueous base and the resulting oil extracted into ether. The ether layer was washed with water until the washings were neutral and dried over anhydrous potassium carbonate. On treatment with maleic acid in ether a yellow solid separated which was recrystallized from isopropanol. This yellow solid had MP 175° to 177°C.
[Brand name]

Proketazine (Wyeth).
[Therapeutic Function]

Tranquilizer
Spectrum DetailBack Directory
[Spectrum Detail]

carfenazine(2622-30-2)1HNMR
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