Befunolol

Chemical compound From Wikipedia, the free encyclopedia

Befunolol (INN) is a beta blocker with intrinsic sympathomimetic activity used in the management of open-angle glaucoma.[1] It also acts as a β adrenoreceptor partial agonist.[2][3] Befunolol was introduced in Japan in 1983 by Kakenyaku Kako Co. under the trade name Bentos.[4]

Trade namesBenfuran, Bentos, Betaclar, Glauconex
ATC code
Quick facts Clinical data, Trade names ...
Befunolol
Clinical data
Trade namesBenfuran, Bentos, Betaclar, Glauconex
AHFS/Drugs.comInternational Drug Names
ATC code
Identifiers
  • (RS)-1-{7-[2-hydroxy-3-(propan-2-ylamino)propoxy]- 1-benzofuran-2-yl}ethanone
CAS Number
PubChem CID
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KEGG
ChEMBL
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC16H21NO4
Molar mass291.347 g·mol−1
3D model (JSmol)
  • O=C(c2oc1c(OCC(O)CNC(C)C)cccc1c2)C
  • InChI=1S/C16H21NO4/c1-10(2)17-8-13(19)9-20-14-6-4-5-12-7-15(11(3)18)21-16(12)14/h4-7,10,13,17,19H,8-9H2,1-3H3 checkY
  • Key:ZPQPDBIHYCBNIG-UHFFFAOYSA-N checkY
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Synthesis

The first reported synthesis of befunolol in 1974 used a benzofuran derivative (4) with epichlorohydrin and then isopropylamine to add the sidechain which was known to produce beta blockers, by analogy with drugs discovered by Imperial Chemical Industries, such as propanolol.[5] The requisite intermediate was synthesized from ortho-vanillin (1) by a condensation reaction with chloroacetone (2) in the presence of potassium hydroxide, giving 2-acetyl-7-methoxybenzofuran (3), which was demethylated using hydrobromic acid.[6][7][8]

References

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