3-trifluoromethyl-pyrazole

Withasomnine Pyrazole, 1-phosphoryl-reactions, 5, 271 Pyrazole, 1-silyl-synthesis, 5, 236 Pyrazole, 1-stannyl-synthesis, 5, 236 Pyrazole, 1-styryl-synthesis, 5, 233 Pyrazole, 1-thienyl-reactions, 5, 268 Pyrazole, 4-(2 -thienyl)-nitration, 5, 238 Pyrazole, 4-(3 -thienyl)-nitration, 5, 238 Pyrazole, trifluoromethyl-synthesis, 5, 284... 

Ttifluowmethylr and Perfluoroalkyl-Substituted Pyrazoles Trifluoromethyl-substituted pyrazoles are readily available through reactions of hydrazines with a,[3-unsaturated trifluoromethyl ketones and trifluoromethylated [3-dicarbonyl compounds. In addition, 1,3-dipoIar addition reactions can be applied. Such transformations have been... 

A large variety of newer poly(ether imide)s has been described. Included among these are perfluorinated polymers (96), poly(ester ether imide)s (97), poly(ether imide)s derived from A/,Ar-diamino-l,4,5,8-naphthalenetetracarboxyHcbisimide (98), and poly(arylene ether imide ketone)s (99). In addition, many other heterocyHc groups have been introduced into polyether systems, eg, poly(pyrazole ether)s (100) and poly(aryl ether phenylquinoxaLine)s (101) poly(aryl ether oxazole)s with trifluoromethyl groups (102) and polyethers with other heterolinkages, eg, poly(arylether azine)s (103). 

Pyrazole, 1 -bis(dimethylamino)phosphino- H NMR, 5, 185 (B-73NMR165, B-75MI40402) Pyrazole, 3,5-bis(trifluoromethyl)-1 -trimethylsilyl-5, 213 <71JOM(27)185)... 

Pyrazole, 3-(trifluoromethyl)-4,5-trimethylene as amebicide, 5, 291 Pyrazole, 3-triflyl-4-phenyl-synthesis, 5, 282 Pyrazole, 1,3,4-triiodo-synthesis, 5, 234 Pyrazole, 1,3,5-trimethyl-isomerization, 5, 221 Pyrazole, 3,4,5-trimethyl-bromination, 5, 240 halogenation, 5, 89 reactions... 

Pyrazole, 3,4,5-tris(trifluoromethyl)-synthesis, 5, 282 Pyrazole, vinyl-reactions, 5, 261 Pyrazole, 1-vinyl-polymerization, 1, 279... 

Likewise, trifluoromethyl-substituted nitrile imines [172] and nitnle oxides [173,174, 7 75] have been used to synthesize tnfluoromethyl substituted five-membered ring systems of the pyrazole, isomzole, isoxazohne, and 1,2,4-oxadiazole... 

An unusual 1,4-migration of a trifluoromethyl group was observed when azomethine imines were synthesized from hexafluoroacetone azine and alkoxy-acetylenes The rearrangement, which occurs at temperatures as low as 0 "C, results in the formation of A-(perfluoro-ferf-butyl)pyrazoles [207] (equation 46)... 

Fluorine-19 NMR has also been used to study annular tautomerism in pyra-zoles, both for fluoro- and for trifluoromethyl-pyrazoles (99H355). Comparison of data chemical shifts and V coupling constants of 64a and 64b]... 

The different nucleophilicities of 3,5-dimethyl- and 3,5-bis(trifluoromethyl) pyrazoles are shown by their reactions widi lraas-[Rh(CO)Cl(Ph3P)2]. The dimethyl derivative gives die dinuclear species similar to 111. The less nucleophilic fluorine derivative gives 116, where die pyrazole ring is monodentate. The fluoro compound similar to 111 [L2 = (CO)2l may be obtained in the absence... 

The 3,5-bis(trifluoromethyl)pyrazolate analog [Ir(cod)(/x-3,5-(CF3)2pz)]2 does not enter into oxidative addition with iodine, methyl iodide, or acetylenes. The mixture of pyrazolate and 3,5-bis(trifluoromethyl)pyrazolate gives [(rj -codllrf/x-pz)(/L-3,5-(CF3)2pz)Ir(rj -cod)], which reacts with bis(trifluoromethyl)acetylene in a peculiar manner [83JCS(CC)580], producing 145, where 3,5-bis(trifluoromethyl) pyrazolate is replaced by the ethylene bridge and the rj -coordination mode of one of the cod ligands is converted into the rj -allylic mode. 

Organ et al. from York University demonstrated that a diarylated IH-pyrazole-based library, based on the structure of the potent COX II inhibitor Celecoxib [4-(3-trifluoromethyl-5-(4-methylphenyl)-lH-pyrazol-l-yl)benzenesulfonamide], could be rapidly prepared using MAOS [59]. Microwave-accelerated Suzuki reaction on 4-(5-iodo-3-methyl-lH-pyrazol-l-yl)-benzenesulfonamide using heterogeneous Pd/C was the principal diversification step investigated (Scheme 41). The interest of the team in microwave... 

Syntheses of fluoro-substituted pyrazoles continue to be of interest. Both 3- and 5-fluoropyrazoles (44 and 45, respectively) can be prepared from 43 <96JOC2763>. Treatment of 43 with hydrazine followed by N-alkylation provides 44, whereas reactions with monosubstituted hydrazines afford 45. The 4-(trifluoromcthyl)pyrazoles 47 are obtained from J-trifluoromethyl vinamidinium salt 46 <96TL1829>. The 5-trifluoromethyl-3-carboethoxypyrazoles 49 are obtained from the 1,3-dipolar cycloadditions of trifluoromethyl alkenes 48 with ethyl diazoacetate <96T4383>. 

Similar ring systems were prepared <97JHC1693> by Coppo and Fawzi from the reaction of substituted ethyl 5-[methyl(methylsulfonyl)amino]-l 7/-pyrazole-4-carboxylates 119 with sodium hydride. This gave the 7-substitued 1,7-dihydro-l-methylpyrazolo[3,4-c][l, 2]thiazin-4(37/)-one 2,2-dioxides 120 in fair to good yield (Scheme 30). They also extended this synthesis by treating methyl 2-[methyl(methylsulfonyl)amino]-6-(trifluoromethyl)-3-pyridinecarboxylate 121 with sodium hydride in dimethylformamide to yield l-methyl-7-(trifhioromethyl)-l//-pyrido[2,3-c][l,2]thiazin-4(3//)-one 2,2-dioxide 122 in 79% yield (Scheme 31) <98JHC499>. 

An efficient route to 4-aryloxy pyrazoles 74 bearing a trifluoromethyl group has been developed from 4-hydroxypyrazole 72 under basic conditions with 3,5-dicyanofluorobenzene 73 with concomitant removal of the silyl group to give pyrazoles 75 <06SL1404>. Fries-type... 

A series of 2-(5-aryl-3-styryl-4,5-dihydro-lA-pyrazol-l-yl)-4-(trifluoromethyl)-pyrimidines 78 was synthesized by the cyclocondensation of 5-aryl-l-carboxamidino-3-styry 1-4,5-dihydro-1 //-pyrazoles 76 with 4-alkoxy-l,l,l-trifluoroalk-3-en-2-ones 77 <06S2349>. 

The thermodynamic properties of 3,5-bis(trifluoromethyl)-l,2,4-triazole have been measured and discussed in the light of the conclusions provided by ab initio calculations (MP2/6-31G //6-31G level of accuracy) applied to trifluoromethyl-substituted triazoles, the parent triazole and pyrazole. It is worth noticing that 21 is more stable than 21a by... 

Shen L, Zhang J, Cao S, Yu JL, Liu NJ, Wu JJ, Qian XH (2008) One-pot synthesis of trifluoromethyl-containing pyrazoles via sequential Yb(PFO)(3)-catalyzed three-component reaction and IBX-mediated oxidation. Synlett 3058-3062... 

Trifluoromethyl-substituted pyrazoles are easily obtained using trifluoromethyl-alkynes as dipolarophiles (Table 8.2, entry 9). Thus, treatment of 4,4,4-trifluorobut-2-ynoic acid with excess diazomethane gave methyl 4-(trifluoromethyl)pyrazole-4-carboxylate (45%) accompanied by its N - (32%) and -methylated (6.5%) derivatives (267). Another convenient route to CF3-substituted pyrazoles involves dipolar cycloaddition of appropriately CF3-substituted alkenes followed by eliminative aromatization (76,77,268). For example, the reaction of alkenes such as (CF3)2C=C(H)COAr with ethyl diazoacetate gave 4-aroyl-5-trifluoromethylpyra-zole-3-carboxylates (268). 

Acetylenedicarboxylic acid esters and related activated alkynes are routinely used as dipolarophiles for diazo dipoles. Recent examples include the use of diazo compounds 20 (49), 23 (51), and 24 (52) (Scheme 8.7), 25 (56) (Scheme 8.8), diazoacetaldehyde dimethylacetal (41) (which after cycloaddition and deprotection gave the corresponding pyrazole-3-carbaldehyde), ethyl 3-diazopyruvate (270), p-tolyl-trifluoromethyldiazomethane (271), bis(trifluoromethyl)diazomethane (272), and diazomethylenephosphoranes (60). 

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