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Leancare Ltd.
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+33 962096793 |
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enquiry@leancare.co.uk |
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| Company Name: |
2A PharmaChem USA
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(630) 737-0988 |
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sales@2apharmachem.com |
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| | Etifelmine Basic information |
| Product Name: | Etifelmine | | Synonyms: | 2-benzhydrylidenebutan-1-amine;2-Diphenylmethylenebutylamine;2-Ethyl-3,3-diphenyl-2-propenylamine;EDPA;Etifelmin;Etifelmine;1-Butanamine, 2-(diphenylmethylene)- | | CAS: | 341-00-4 | | MF: | C17H19N | | MW: | 237.34 | | EINECS: | | | Product Categories: | | | Mol File: | 341-00-4.mol |  |
| | Etifelmine Chemical Properties |
| | Etifelmine Usage And Synthesis |
| Originator | Etifelmine,Giulini,W. Germany,1963 | | Definition | ChEBI: Etifelmine is a diarylmethane. | | Manufacturing Process | (a) Preparation of 2-ethyl-3-hydroxy-3,3-diphenyl-propylamine: 10 g of 2-
ethyl-3-hydroxy-3,3-diphenyl-propionitrile are dissolved in 200 ml of
methanol. 10 ml of acetic acid are added to the mixture, and the mixture is
hydrogenated in the presence of platinum as catalyst. After the hydrogen
uptake or consumption has ceased, the reaction is interrupted, the catalyst is
filtered off and the filtrate is evaporated in vacuo to dryness. The residue is
dissolved in water and, after the addition of 1 ml of hydrochloric acid, the
solution extracted with ether. The acidified ether-phase is discarded. The
aqueous phase is made alkaline with ammonia, whereby the base crystallizesout. The crystals are recovered and recrystallized from methanol. The melting
point of the 2-ethyl-3-hydroxy-3,3-diphenyl-propylamine thereby obtained is
132°C.
(b) Preparation of 2-ethyl-3,3-diphenyl-1-amino-propene-(2)-hydrochloride: 5
g of 2-ethyl-3-hydroxy-3,3-diphenyl-propylamine are dissolved in 50 ml of
acetic acid. Gaseous hydrogen chloride is passed through the solution for 10
minutes, and thereafter the solution is boiled for one hour under reflux. The
solution is then distilled to dryness. The residue is dissolved in water and the
acidified solution extracted with ether. The aqueous phase is separated, made
alkaline with ammonia and extracted with ether. The ether phase is dried over
sodium sulfate, the ether distilled off and the residue is dissolved in
methanolic hydrogen chloride. On the addition of absolute ether, the
hydrochloride of 2-ethyl-3,3-diphenyl-1-amino-propene-(2) is crystallized out.
The crystalline substance thereby obtained has a melting point of 232°C. | | Therapeutic Function | Central stimulant, Antihypotensive |
| | Etifelmine Preparation Products And Raw materials |
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