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Orciprenaline sulfate

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Orciprenaline sulfate Basic information

Product Name:
Orciprenaline sulfate
Synonyms:
  • 1-(3,5-dihydroxyphenyl)-1-hydroxy-2-isopropylaminoethanesulfate
  • 1-(3,5-dihydroxyphenyl)-2-(isopropylamino)ethanolsulfate
  • 3,5-dihydroxy-alpha-((isopropylamino)methyl)benzylalcoholsulfate
  • 3,5-dihydroxy-alpha-((isopropylamino)methyl)-benzylalcohosulfate(2:1)(s
  • 3-benzenediol,5-(1-hydroxy-2-((1-methylethyl)amino)ethyl)-sulfate(2:1)
  • alotec
  • metaprel
  • novasmasol
CAS:
5874-97-5
MF:
C22H36N2O10S
MW:
520.59
EINECS:
227-539-6
Product Categories:
  • Adrenergics
  • Agonists
  • Neurotransmitters
  • Amines
  • Aromatics
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
  • 5874-97-5
Mol File:
5874-97-5.mol
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Orciprenaline sulfate Chemical Properties

Melting point:
202-203°
storage temp. 
2-8°C
solubility 
Freely soluble in water, slightly soluble in ethanol (96 per cent), practically insoluble in methylene chloride.
form 
Solid
color 
White to Off-White
Stability:
Hygroscopic
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Safety Information

Hazard Codes 
Xn
Risk Statements 
20
Safety Statements 
36
WGK Germany 
2
RTECS 
DO2275000
HS Code 
2922504500
Toxicity
LD50 in rats (mg/kg): 42 orally (Goldenthal)

MSDS

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Orciprenaline sulfate Usage And Synthesis

Chemical Properties

White or almost white, slightly hygroscopic, crystalline powder.

Originator

Alupent, Boehringer Ingelheim ,W. Germany ,1961

Uses

Beta2-adrenoceptor agonist; bronchodilator.

Uses

Bronchodilatator;Beta-adrenergic agonist

Manufacturing Process

In an initial operation, 3,5-diacetoxyacetophenone was reacted first with bromine and then with isopropylamine to give 1-(3,5-dihydroxyphenyl)-2- isopropylaminoethanone.
59 g of 1-(3,5-dihydroxy-phenyl)-2-isopropylaminoethanone (free base) were dissolved in 590 cc of methanol, and the solution was hydrogenated in the presence of about 80 g Raney nickel at room temperature and under a pressure of 5 atm. Hydrogen absorption was terminated after a few minutes. The catalyst was separated by vacuum filtration, and the filtrate, an ethanolic solution of 1-(3,5-dihydroxyphenyl)-1-hydroxy-2-isopropylaminoethane, was admixed with the calculated amount of an alcoholic 20% sulfuric acid solution. A crystalline precipitate formed which was filtered off and washed with alcohol. For purification, the product was dissolved in water and the solution was filtered through iron-free charcoal.
Thereafter, the filtrate was evaporated to dryness in vacuo and the residue was taken up in alcohol. The crystalline precipitate which separated out after some standing was separated by vacuum filtration and washed with alcohol. After recrystallization from 90% alcohol, 61 g (83.2% of theory) of 1-(3,5- dihydroxyphenyl)-1-hydroxy-2-isopropylamino-ethane sulfate, MP 202° to 203°C, was obtained.

brand name

Alupent (Boehringer Ingelheim); Prometa (Muro).

Therapeutic Function

Bronchodilator

Pharmacokinetics

Metaproterenol is a direct-acting resorcinol analogue of isoproterenol. The N-isopropyl is β-directing, and the combination with the resorcinol ring system enhances the selectivity for the β2-receptors. It is the least potent of the β2-selective agonists, however, most likely because of the poor β2-selectivity of the isopropyl group. It has good oral bioavailability being resistant to COMT and only slowly metabolized by MAO. When administered orally, it has an onset of approximately 30 minutes with a 4-hour duration. Inhaled metaproterenol can have an onset as quick as 5 minutes; however, it can be as long as 30 minutes in susceptible individuals. Metaproterenol is available in tablet, syrup, and inhalation dosage forms and is recommended for bronchial asthma attacks and treatment of acute asthmatic attacks in children 6 years of age and older (5% solution for inhalation only). Metaproterenol has the same adverse effect profile as other adrenergic agonists, but with a decreased incidence of arrhythmias.

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