Dapoxetine

Dapoxetine Struktur
119356-77-3
CAS-Nr.
119356-77-3
Englisch Name:
Dapoxetine
Synonyma:
DAPOXETIN;DAPOXTINE;Dapoxetina;Dapoxetine base;D-Dapoxetine HCL;Dapoxetine (Free Base);(S)-N,N-DiMethyl-3-(naphthalen-1-yloxy)-1-phenylpropan-1-aMine;Detoxetine;DAPOXETINE;Dapoxetinum
CBNumber:
CB4346685
Summenformel:
C21H23NO
Molgewicht:
305.41
MOL-Datei:
119356-77-3.mol

Dapoxetine Eigenschaften

Schmelzpunkt:
48 - 49°C
Siedepunkt:
454.4±38.0 °C(Predicted)
Dichte
1.081±0.06 g/cm3(Predicted)
storage temp. 
-20°C Freezer
Löslichkeit
Chloroform (Slightly), DMSO (Slightly, Heated), Methanol (Slightly)
Aggregatzustand
Solid
pka
8.38±0.50(Predicted)
Farbe
White to Pale Beige
CAS Datenbank
119356-77-3(CAS DataBase Reference)

Sicherheit

Dapoxetine Chemische Eigenschaften,Einsatz,Produktion Methoden

Verwenden

Dapoxetine-d7 Hydrochloride is a Labelled Dapoxetine (D185700). A selective serotonin reuptake inhibitor (SSRI).

Clinical Use

Dapoxetine is a selective serotonin re-uptake inhibitor (SSRI) which has been approved in Finland and Sweden for the treatment of premature ejaculation.Dapoxetine was discovered and developed by Lilly and was licensed to Alza, a wholly-owned subsidiary of Johnson & Johnson.

Synthese

Several synthetic routes for the preparation of dapoxetine have been disclosed, all on gram scale. Based on the routes and yields, the most likely process route is described in the scheme 4. Commercially available (R)-(+)-3-chloro-1-phenyl- 1-propanol (19) was reacted with 1-naphthol in the presence of 50% aqueous sodium hydroxide in DMF to give ether 20 in 90% yield. Activation of the secondary alcohol was accomplished through treatment of 20 with methane sulfonyl chloride and triethylamine with catalytic DMAP. Upon complete conversion to the corresponding mesylate, dimethylamine was added to the reaction mixture. The addition of hydrochloric acid in ethyl acetate to the resultant crude product gave dapoxetine hydrochloride (IV) in 67% yield. Purification of this material by re-crystallization from isopropanol provided IV in 86% yield and in 99.6% ee.

Synthesis_119356-77-3

Dapoxetine Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Dapoxetine Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 371)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
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119356-77-3()Verwandte Suche:


  • (S)-(+)-Dapoxetine
  • Dapoxetine-d7 HCl
  • Dapoxetine hydrochloride (S-(+)-N,N-Dimethyl-a-[2-(naphthalenyloxy)ethyl]benzenemethanamine hydrochloride
  • Detoxetine
  • (S)-(+)-N,N-dimethyl-a-(2-(naphthalenyloxy)ethyl)benzenemethanamine
  • DAPOXETINE
  • (S-(+)-N,N-Dimethyl-a-[2-(naphthalenyloxy)ethyl]benzenemethanamine hydrochloride
  • (S-(+)-N,N-DiMethyl-a-[2-(naphthalenyloxy)ethyl]benzeneMethanaMine hydrochloride Dapoxetine hydrochloride
  • Methylaminophenylacetone hydrochloride
  • Dapoxetine right
  • (S-(+)-N,N-DiMethyl-a-[2-(naphthalenyl
  • apoxetine hydrochloride
  • (1S)-N,N-dimethyl-3-naphthalen-1-yloxy-1-phenylpropan-1-amine
  • Dapoxetinum
  • Benzenemethanamine, N,N-dimethyl-α-[2-(1-naphthalenyloxy)ethyl]-, (αS)-
  • Dapoxetine Solution, 100μg/mL
  • Dapoxetine USP/EP/BP
  • Dapoxetine-D7 hydrochloride
  • (+)-N,N-Dimethyl-1-phenyl-3-(1-naphtalenyl oxy) propanamine (Dapoxetine free base)
  • Dapoxetine Powder/Dapoxetine Raw Material for Sexual Enhancement
  • Dapoxetine-1 gram
  • DapoxetineQ: What is Dapoxetine Q: What is the CAS Number of Dapoxetine Q: What is the storage condition of Dapoxetine Q: What are the applications of Dapoxetine
  • DAPOXETIN
  • Dapoxetine base
  • (S)-N,N-DiMethyl-3-(naphthalen-1-yloxy)-1-phenylpropan-1-aMine
  • Dapoxetine (Free Base)
  • Dapoxetina
  • DAPOXTINE
  • D-Dapoxetine HCL
  • Dapoxetine Sex Enhancer Raw Powder
  • Benzenemethanamine, N,N-dimethyl-α-[2-(1-naphthalenyloxy)ethyl]-, (αS)-
  • 119356-77-3
  • 11935-77-3
  • 19356-77-3
  • 119356-77-1
  • 11356-77-3
  • 119356-77-0
  • CHNOHCl
  • C21H23NO
  • Erectile Dysfunction
  • API
  • Dapoxetine hydrochloride
  • A
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