| Identification | Back Directory | [Name]
pecazine | [CAS]
60-89-9 | [Synonyms]
Paxital
Pecatal
Lacumin
Mepazin
pecazine
Pacazine
MEPAZINE
Ai3-50131
Nothiazine
Einecs 200-490-8
2975-36-2 (Mono-hydrochloride)
(N-Methyl-3-piperidyl)methylphenothiazine
10-(1-Methylpiperidyl-3-methyl)phenothiazine
10-(1-Methyl-3-piperidyl)methyl phenothiazine
10-[(1-Methyl-3-piperidinyl)methyl]-10H-phenothiazine
10H-Phenothiazine, 10-((1-methyl-3-piperidinyl)methyl)- | [EINECS(EC#)]
200-490-8 | [Molecular Formula]
C19H22N2S | [MOL File]
60-89-9.mol | [Molecular Weight]
310.46 |
| Chemical Properties | Back Directory | [Melting point ]
80°C | [Boiling point ]
bp4 230-235° | [density ]
1.1252 (rough estimate) | [refractive index ]
1.6270 (estimate) | [storage temp. ]
Hygroscopic, Refrigerator, under inert atmosphere | [Water Solubility ]
5.588mg/L(24 ºC) |
| Hazard Information | Back Directory | [Originator]
Pacatal,Warner Lambert,US,1957 | [Uses]
Pecazine Hydrochloride acts as an anti-HIV agent in the form of C-C chemokine inhibitors. | [Definition]
ChEBI: Pecazine is a member of phenothiazines. | [Manufacturing Process]
A 500 cc flask equipped with a mechanical stirrer, reflux condenser and a soda-lime tube was filled with 230 cc of absolute xylene, 27.5 g of 1-methyl3-bromomethylpiperidine, 53.3 g of phenothiazine and 14.2 g of finely powdered sodium amide, and the solution was heated under reflux for 6 hours. After cooling water was added and the batch was extracted with ether. As the hydrochloric acid salt of the obtained phenothiazine derivative is difficultly soluble in water, the further processing was carried out by way of the acetate. The etheric solution was extracted several times in a separating funnel with dilute acetic acid. The combined aqueous extracts were basified, extracted with ether, dried with potassium carbonate and, after removal of the ether, distilled in vacuo.
Yield = 64%; boiling point 230°C to 235°C at 4 mm; melting point of
hydrochloride is 180°C to 181°C. | [Therapeutic Function]
Tranquilizer |
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