10-[(1-methyl-3-piperidyl)methyl]-10H-phenothiazine monohydrochloride

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Products Intro: Product Name:10-((1-methylpiperidin-3-yl)methyl)-10H-phenothiazine hydrochloride
CAS:2975-36-2
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CAS:2975-36-2
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CAS:2975-36-2
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Products Intro: Product Name:10-((1-methylpiperidin-3-yl)methyl)-10H-phenothiazine hydrochloride
CAS:2975-36-2
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10-[(1-methyl-3-piperidyl)methyl]-10H-phenothiazine monohydrochloride Basic information
Product Name:10-[(1-methyl-3-piperidyl)methyl]-10H-phenothiazine monohydrochloride
Synonyms:10-[(1-methyl-3-piperidyl)methyl]-10H-phenothiazine monohydrochloride;10-((1-methylpiperidin-3-yl)methyl)-10H-phenothiazine hydrochloride;10H-Phenothiazine, 10-[(1-methyl-3-piperidinyl)methyl]-,monohydrochloride;Mepazine hydrochloride
CAS:2975-36-2
MF:C19H23ClN2S
MW:346.91732
EINECS:221-020-8
Product Categories:
Mol File:2975-36-2.mol
10-[(1-methyl-3-piperidyl)methyl]-10H-phenothiazine monohydrochloride Structure
10-[(1-methyl-3-piperidyl)methyl]-10H-phenothiazine monohydrochloride Chemical Properties
Melting point 180-181 °C
Boiling point 180-183 °C(Press: 0.5 Torr)
storage temp. Store at -20°C
solubility DMSO: 50 mg/mL (144.13 mM)
Safety Information
MSDS Information
10-[(1-methyl-3-piperidyl)methyl]-10H-phenothiazine monohydrochloride Usage And Synthesis
OriginatorPacatal,Warner Lambert,US,1957
Manufacturing ProcessA 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 FunctionTranquilizer
10-[(1-methyl-3-piperidyl)methyl]-10H-phenothiazine monohydrochloride Preparation Products And Raw materials
Raw materialsSodium amide-->Phenothiazine-->Acetic acid
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