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Electrophilic Cyclisations of 3-Arylpenta-1,4-diyn-3-ols for the Synthesis of Heterocycles

Wilson, Rebecca (2020) Electrophilic Cyclisations of 3-Arylpenta-1,4-diyn-3-ols for the Synthesis of Heterocycles. Doctoral thesis, University of Huddersfield.

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Abstract

This project was concerned with investigating the electrophilic cyclisation reactions of 3-phenylpenta-1,4-diyn-3-ols possessing either an ortho-N-linked-or an ortho-S-linked-sulfonamide function. Cyclisations of both series of sulfonamides meditated by alkynophilic initiators [e.g. I2, ICl, AgOAc or In(OTf)3] provided access to novel functionalised heterocycles.

Thus, addition of methyl 2-(arenesulfonamido)benzoates to alkynyllithium reagents furnished 3-[(2-arenesulfonamido)phenyl]penta-1,4-diyn-3-ols in which the alkyne termini possess identical substituents. Dialkynols having unsymmetrical alkyne terminal groups have been obtained from the addition of an alkynyllithium reagent or HC≡CMgBr to 3-aryl-1-(2-tosylamidophenyl)prop-2-yn-1-ones. The ortho-S-linked sulfonamides have been accessed directly from N-substituted saccharins that readily add alkynyllithiums to provide 3-(2-sulfamoylphenyl)penta-1,4-diyn-3-ols in good yields.

Desilylation (5M NaOH in MeOH) of 1,5-bis(trimethylsilyl)-3-(2-tosylamidophenyl)penta-1,4-diyn-3-ol also triggered cyclisation via a 5-exo-digpathway and gave a quantitative yield of 3-ethynyl-2-methylene-1-tosylindolin-3-ol. However, when both silyl functions were replaced with either a propyl-or a phenyl-group, cyclisation to the 1-tosylindolin-3-ol did not occur with base. A quantitative yield of 3-(phenylethynyl)-1-tosyl-1H-indol-2-yl(1-phenyl)methanol was obtained from treatment of 1,5-diphenyl-3-(2-tosylamidophenyl)penta-1,4-diyn-3-ol with AgOAc in MeCN. The analogous reaction with 6-(2-tosylamidophenyl)undeca-4,7-diyn-6-ol, provided 1-[3-(pent-1-yn-1-yl]-1-tosyl-1H-indol-2-yl)butan-1-ol, together with smaller amounts of (E)-2-but-1-en-1-yl-3-pentyn-1-yl-1-tosyl-1H-indole and 4-pentyn-1-yl-2-propylquinoline. It was found that when 3-(2-tosylamidophenyl)penta-1,4-diyn-3-ols possessed bulky groups on the alkyne units, the reaction followed an alternative course giving access to the(Z)-2-benzylidene-, (Z)-2-(2,2-dimethylpropylidene)-and (Z)-2-(trimethylsilylmethylene)-derivatives of 3-alkynyl-1-tosylindolin-3-ols. Mechanisms to account for these outcomes have been proposed. Contrasting behavior was observed from the In(OTf)3-mediated cyclisation of 1,5-diphenyl-3-(2-tosylaminophenyl)penta-1,4-diyn-3-ol, which promoted an unexpected and remarkable cascade pathway leading to 2,4-diphenyl-1-tosyl-4,5-dihydrofuro[2,3-c]quinoline, albeit in moderate yield.

Attempted iodocyclisation (ICl in MeCN) of 1,5-diphenyl-3-[2-(N-methylsulfamoyl)phenyl]penta-1,4-diyn-3-ol resulted only in cyclodehydration to give the novel 3,3-bis(phenylethynyl)-2-methyl-1,2-benzisothiazole 1,1-dioxide. However, application of these conditions to 1,5-diphenyl-3-[2-(N-p-tolylsulfamoyl)phenyl]penta-1,4-diyn-3-ol provided a novel derivative of the unusual 1,2-benzisothiazolo[2,3-a]quinoline system that was characterised by X-ray crystallography; the corresponding 2-aryl-3,3-di(alkynyl)-1,2-benzisothiazole 1,1-dioxide was also formed. The latter also underwent iodocyclisation to give the 1,2-benzisothiazolo[2,3-a]quinolines. It was established that the 3,3-di(alkynyl)-1,2-benzisothiazole 1,1-dioxides could be generated most efficiently by treatment of the 3-[2-(sulfamoyl)phenyl]penta-1,4-diyn-3-ols with In(OTf)3in DCM.

Iodocyclisation (ICl in MeCN) of 3-(2-tosylamidophenyl)penta-1,4-diyn-3-ols having symmetrical alkyne substituents afforded novel 4-alkynyl-3-iodoquinolines. However, the unsymmetrically-substituted pentadiynols cyclised less efficiently to give, in some cases, mixtures of regioisomeric 3-iodoquinolines. The cyclisation of 1-(4-methoxyphenyl)-5-phenyl-3-(2-tosylamidophenyl)penta-1,4-diyn-3-ol regiospecifically generated 3-iodo-2-(4-methoxyphenyl)-4-(phenylethynyl)quinoline, as anticipated.

Silver-catalysed cyclisation (AgOAc in MeCN) of 3-[2-(N-arylsulfamoyl)phenyl]penta-1,4-diyn-3-ols proceeds stereoselectively to (Z)-3-alkylidene-4-alkynyl-2-aryl-and (Z)-4-alkynyl-2-aryl-3-arylidene-1,2-benzothiazin-4-ol 1,1-dioxides via a 6-endo-digpathway in good to excellent yields, constituting a new approach to this ring system. Two of the pentadiynols also furnished 1,2-benzothiazepine 1,1-dioxides derived via a 7-endo-digring closure. Mechanisms for the formation of these novel compounds are proposed.

With a range of heterocycles to hand some were subjected to functionalisation or annulation reactions. Of note is the Pd-mediated domino-amination-hydroamination of 4-alkynyl-3-iodoquinolines with a range of primary amines. This approach was exploited to access novel 2,3,4-trisubstituted pyrrolo[2,3-c]quinolines, analogues of the biologically active Marinoquinolines. However, in some instances the hydroamination step was suppressed and the major or exclusive product was a 4-alkynyl-3-amino-2-arylquinoline.

Suzuki-Miyaura couplings to 4-alkynyl-2-iodo-3-arylquinolines and efforts to effect iodocyclisations of the products are also described.

Item Type: Thesis (Doctoral)
Subjects: Q Science > QD Chemistry
Schools: School of Applied Sciences
Depositing User: Christine Morelli
Date Deposited: 22 Jun 2021 14:30
Last Modified: 28 Aug 2021 14:21
URI: http://eprints.hud.ac.uk/id/eprint/35533

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