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Sulfinalol

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Sulfinalol
Names

IUPAC name 4-[1-Hydroxy-2-[4-(4-methoxyphenyl)butan-2-ylamino]ethyl]-2-methylsulfinylphenol
Identifiers
CAS Number	66264-77-5^Y
3D model (JSmol)	Interactive image
PubChem CID	44439
UNII	PH7O14792O^Y
CompTox Dashboard (EPA)	DTXSID80867219
InChI InChI=1S/C20H27NO4S/c1-14(4-5-15-6-9-17(25-2)10-7-15)21-13-19(23)16-8-11-18(22)20(12-16)26(3)24/h6-12,14,19,21-23H,4-5,13H2,1-3H3 Key: PAQZZCOZHPGCFW-UHFFFAOYSA-N
SMILES CC(CCC1=CC=C(C=C1)OC)NCC(C2=CC(=C(C=C2)O)S(=O)C)O
Properties
Chemical formula	C₂₀H₂₇NO₄S
Molar mass	377.50 g·mol⁻¹
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

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Sulfinalol is a beta adrenergic receptor antagonist.^[1]

Synthesis[edit]

The methyl group on a sulfoxide is sufficiently acidic to substitute for phenolic hydroxyl.

Sulfinalol synthesis:^[2] R. E. Philion, (1978 to Sterling), C.A. 90, 137468 (1979).

The preparation of this combined α- and β-blocker sulfinalol begins by protection of the phenolic hydroxyl as its benzoate ester. Bromination followed by condensation with 4-(4-methoxyphenyl)butan-2-amine (not PMA) gives the aminoketone 3. Successive catalytic reduction and saponification affords aminoalcohol 4. Oxidation of the sulfide to the sulfoxide with a reagent such as metaperiodate gives sulfinalol (5).

References[edit]

^ Sybertz, E. J.; Baum, T.; Pula, K. K.; Nelson, S.; Eynon, E.; Sabin, C. (1982). "Studies on the mechanism of the acute antihypertensive and vasodilator actions of several beta-adrenoceptor antagonists". J. Cardiovasc. Pharmacol. 4 (5): 749–58. doi:10.1097/00005344-198209000-00009. PMID 6182405. S2CID 34100646.

^ DE 2728641, Philion, Richard Everett, "4-Hydroxyphenylalkanolaminderivate und Verfahren zu deren Herstellung [4-Hydroxyphenylalkanolamine derivatives and processes preparation thereof]", published 1978-01-05, assigned to Sterling Drug Inc.