Basic information Safety Supplier Related

Amosulalol Hcl

Basic information Safety Supplier Related

Amosulalol Hcl Basic information

Product Name:
Amosulalol Hcl
Synonyms:
  • ( -)-5-Hydroxy-2-(2-(2-methoxyphenoxy)ethylamino)ethyl)-2-methylbenzolsulfonamid hydrochlorid
  • Amosulalol monohydrochloride
  • Benzenesulfonamide, 5-(1-hydroxy-2-((2-(2-methoxyphenoxy)ethyl)amino)ethyl)-2-methyl-, hydrochloride, (+-)-
  • 5-(1-Hydroxy-2-((2-(2-Methoxyphenoxy)ethyl)aMino)ethyl)-2-MethylbenzenesulfonaMide hydrochloride
  • Amosulalol Hcl
  • AMOSULALOL HYDROCHLORIDE
CAS:
93633-92-2
MF:
C18H25ClN2O5S
MW:
416.9195
Mol File:
93633-92-2.mol
More
Less

Amosulalol Hcl Chemical Properties

Melting point:
158-160°
pka
pK1 7.4; pK2 10.2(at 25℃)
More
Less

Amosulalol Hcl Usage And Synthesis

Originator

Amosulalol hydrochloride,Yamanouchi

Uses

Amosulalol Hydrochloride is used in studies to evaluate the effect of α1-blocker doxazosin on diabetic nephropathy -comparison with α,β -blockers.

Definition

ChEBI: Amosulalol hydrochloride is a sulfonamide.

Manufacturing Process

A mixture of N-benzyl-2-(2-methoxyphenoxy)ethylamine, methyl ethyl ketone, and 5-bromoacetyl-2-methylbenzenesulfonamide was refluxed with stirring. After cooling the reaction mixture, ethyl ketone was distilled off under reduced pressure and the residue formed was dissolved in benzene. Then, ether was added to the solution and after removing the hydrobromide of N-benzyl-2-(2- methoxyphenoxy)ethylamine precipitated, the solvent was distilled off under reduced pressure to provide a viscous oily product.
The viscous oily product was dissolved in ethanol and after adding to the solution an excess amount of sodium borohydride, the mixture was stirred at room temperature followed by distilling off ethanol under reduced pressure. The residue was dissolved in ethyl acetate and the ethyl acetate layer recovered was washed with water, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to provide a viscous oily product. The product was subjected to a silica gel column chromatography and eluted using benzene and then a mixture of benzene and ethyl acetate of 10:1 by volume ratio to provide 5-{1-hydroxy-2-[N-benzyl-2-(2- methoxyphenoxy)ethylamino]ethyl}-2-methyl-benzenesulfonamide as a viscous oily product.
In 200 ml of methanol was dissolved 20.0 g of 5-{1-hydroxy-2-[N-benzyl-2- (2-methoxyphenoxy)ethylamino]ethyl}-2-methyl-benzenesulfonamide. After adding thereto 20 ml of ethanol containing about 10% hydrogen chloride and 1.0 g of 10% palladium charcoal, the mixture was shaken in hydrogen gas stream. When the absorption of hydrogen stopped, the catalyst was filtered away and the filtrate was distilled off under reduced pressure. The residue was dissolved in 100 ml of ethanol while it was hot and the solution was allowed to stand overnight in ice chamber, whereby 12.8 g of the α-type crystals of 5-{1-hydroxy-2-[2-(2-methoxyphenoxy)ethylamino]ethyl}-2- methylbenzenesulfonamide were obtained as the colorless crystals, melting point 169°-171°C.
In practice it is usually used as monohydrochloride

Therapeutic Function

Alpha-adrenergic blocker, Beta-adrenergic blocker, Antihypertensive

Amosulalol HclSupplier

TargetMol Chemicals Inc.
Tel
+1-781-999-5354 +1-00000000000
Email
marketing@targetmol.com
TargetMol Chemicals Inc.
Tel
15002134094
Email
marketing@targetmol.cn
Alchem Pharmtech,Inc.
Tel
8485655694
Email
sales@alchempharmtech.com
TargetMol Chemicals Inc.
Tel
+8613564774135
Email
zijue.cai@tsbiochem.com
Hangzhou MolCore BioPharmatech Co.,Ltd.
Tel
+86-057181025280; +8617767106207
Email
sales@molcore.com
More
Less

Amosulalol Hcl(93633-92-2)Related Product Information