Procaterol

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Procaterol
(±)-Procaterol Enantiomers Structural Formula.png
Systematic (IUPAC) name
(±)-(1R,2S)-rel-8-Hydroxy-5-[1-hydroxy-2-(isopropylamino)butyl]-quinolin-2(1H)-one
Clinical data
AHFS/Drugs.com Micromedex Detailed Consumer Information
Routes of
administration
Oral, inhalation
Identifiers
CAS Number 59828-07-8 YesY
ATC code R03AC16 (WHO) R03CC08
PubChem CID: 4916
ChemSpider 599984 N
UNII X7I3EMM5K0 YesY
KEGG D08424 YesY
Chemical data
Formula C16H22N2O3
Molecular mass 290.357 g/mol
  • CC(C)NC(CC)C(O)c2ccc(O)c1NC(=O)C=Cc12
 NYesY (what is this?)  (verify)

Procaterol, applied as procaterol hydrochloride (USAN), is an intermediate-acting β2-adrenergic receptor agonist used for the treatment of asthma. It has never been filed for FDA evaluation in the United States, where it is not marketed. The drug is readily oxidised in the presence of moisture and air, making it unsuitable for therapeutic use by inhalation.[1] Pharmaceutical company Parke-Davis/Warner-Lambert researched a stabilizer to prevent oxidation, but an effective one was never developed.[1]

Synthesis

Like pirbuterol, procaterol exhibits similar broncholytic properties as albuteral, but it has somewhat of a more prolonged action. It is recommended for use as an inhaled drug for treating bronchial asthma.

Procaterol synthesis:[2][3][4][5][6]

8-Hydroxycarbostyril is acylated with 2-bromobutyric acid chloride at the fifth position of the quinoline system, which gives the compound 3. This undergoes action of isopropylamine, forming an aminoketone, the carbonyl group of which is reduced by sodium borohydride, giving procaterol.

Synonyms of this drug are onsukil, masacin, procadil, meptin, and others.

References

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  2. K. Nakagawa, S. Yoshizaki, Ger. Pat., DE 2461596  (1975).
  3. K. Nakagawa, S. Yoshizaki, U.S. Patent 4,026,897 (1977).
  4. S. Yoshizaki, M. Osaki, K. Nakagawa, Y. Yamura, Chem. Pharm. Bull., 28, 3441 (1980).
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