Heterocyclic thioethers

A new alternative has also been described. The furan is oxidatively meth-oxylated, and the product condensed with an alkyl or arylthiol by means of an acid catalyst in acetonitrile at ordinary temperatures it is presumed that a carbocation is intermediate. Although the method makes available aryl thioesters as well as alkyl thioethers, heterocyclic thiols and thiourea fail. The furylthioethers are not very stable and decompose if the reaction is prolonged.202... 

Thioethers can be obtained either by heterocyclization (Chapter II) or from the reaction between 2-halothiazoles (102) and the sodium salt of... 

Corrosion inhibition is primarily associated with acidizing. Buffered hydrofluoric acid compositions have been shown to be less corrosive (147). Corrosion inhibitors are designed to reduce the rate of reaction of fluid with metal surfaces, generally by forming films on the surfaces. Acetylenic alcohols and amines are frequently components of corrosion inhibitor blends. Other compounds that have been used include nitrogen heterocyclics, substituted thioureas, thiophenols, and alpha-aminoalkyl thioethers (148). 

Jonsson D, Warrington BH, Ladlow M (2004) Automated flow-through synthesis of heterocyclic thioethers. J Comb Chem 6 584—595... 

Intramolecular cyclization of 2-lithiobenzyl-2-halophenyl amines, ethers, and thioethers—Synthesis of phenanthridine, dibenzopyran, and dibenzothiopyran derivatives Having demonstrated the efficiency of this methodology for the preparation of indole derivatives, we prepared the 2-fluoro-phenyl ether and thioether 22 a, b to study their potential as substrates that could afford oxygen and sulfur heterocycles. However, treatment of 22 a, b with fBuLi afforded, after... 

Scheme 7. Preparation of benzo-fused six-membered heterocycles 26-30 and 33 from 2-halophenyl 2-bromobenzyl ethers, amines, and thioether 25 and 32. i) fBuLi (3.5 equiv for 25a, b, 3.3 equiv for 25c,d, and 32), THF, -110 20°C ii)E+, -78 20°C iii) for X = N(allyl), DIBAL-H (1.5 equiv), cat. [NiCl2(dppp)], toluene, 20 °C.

Further, a large number of examples with simple alkyl substituents [168, 171, 176-184], cyclic alkanes [185], aryl substituents [177, 186-192], olefmic substituents [78, 177, 193-196], deuterated compounds [172], thioether groups [171], ester groups [197], orthoesters [198, 199], acetals [168, 182, 200-204], silyl-protected alcohols [198, 205-211], aldehydes [212], different heterocycles [213-217], alkyl halides [218, 219] and aryl halides [192, 220-223] have been reported. A representative example is the reaction of 92, possessing a free hydroxyl group, an acetal and a propargylic ether, to 93 [224] (Scheme 1.40). 

The heterocyclic component in the leaving group offers possibilities for introduction of chirality. Optically active oxazolin-2-yl and thiazolin-2-yl allyl thioethers 7 were thus chosen as substrates (Scheme 8.8) [17]. 

Cimetidine contains an imidazole ring comparable to histamine, a sulfur atom (thioether group) in the side-chain, and a terminal functional group based upon a guanidine (see Section 4.5.4). Ranitidine bears considerable similarity to cimetidine, but there are some important differences. The heterocycle is now furan rather than imidazole, and the guanidine has been modified to an amidine (see Section 4.5.4). A newer drug, nizatidine, is a variant on ranitidine with a thiazole heterocyclic ring system. 

Simple side-chain reactions of 1,2-dithiin diols have been conducted. Besides the formation of esters, ethers (R = Me, Et, 7-Pr, cyclopropyl, Ph, pyridyl, cyclopentyl), and thioethers (R = H, TBDMS R = 4 -(4-hydroxyphenyl)-l//-tetrazole-5-thiol), selective oxidation of the primary alcohol groups in the presence of the 1,2-dithiin heterocycle could be readily achieved (Scheme 36) <1995JME2628, 1994SL201>. Additionally, amides, ureas, and carbamates of the dithiin diol were synthesized <1995JME2628>. 

Substituents attached to a heterocyclic ring through a sulfur atom exist in wider variety than those through oxygen. Besides the simple thio analogues—the thiols (mercaptans), thioethers, thioesters and the like—they include compounds of various higher oxidation states of sulfur, including sulfoxides, sulfones, sulfinic and sulfonic acids and their derivatives. 

Yet another approach to these compounds consists of substituting the piperazine ring onto the preformed heterocyclic moiety. Ullman condensation of the substituted thiosalyciclic acid (40-1) with ort/zo-chloronitrobenzene results in the displacement of chlorine by thiophenoxide and the formation of the thioether (40-2). The nitro group in this last intermediate is then reduced to an aniline (40-3) the resulting amino acid is then cyclized thermally to the lactam (40-4). Treatment of that with phosphorus oxychloride gives the imino chloride (40-5). Reaction with N-methylpiperazine leads to the replacement of chlorine by nitrogen and the formation of clothiapine (40-6) [39]. 

Selective electrofluorinations of activated -positions in thioethers, sulphides, selenides and heterocycles have been reported by a number of workers [34 - 38]. 

---