1,2,3-Triazolines

Three skeleton atoms of a hetero-l,3-diene are incorporated into a five-membered ring system on reaction with 1,2 [n,n] compounds (e.g., hydrazines, reaction type 4, equation 10). On further heating in the presence of azobisiso-butyronitrile (AIBN), the bis(trifluoromethyl)-substituted 1,2,4-triazolines are transformed into 5-tnfluoromethyl-l,2,4-triazoles in high yield [t02 (equation 22). 

Preparation of cholesta-5,7-diene-ia,3/3-diol a solution of 500 mg of the 1,4-cyclized adduct of cholesta-5,7-dien-3/3-ol-ia,2a-epoxideand 4-phenyl-1,2,4-triazoline-3,5-dione in 40 ml of tetrahydrofuran is added dropwise under agitation to a solution of 600 mg of lithium aluminum hydride in 30 ml of THF. Then, the reaction mixture liquid Is gently refluxed and boiled for 1 hour and cooled, and a saturated aqueous solution of sodium sulfate is added to the reaction mixture to decompose excessive lithium aluminum hydride. The organic solvent layer is separated and dried, and the solvent Is distilled. The residue Is purified by chromatography using a column packed with silica gel. Fractions eluted with ether-hexane (7 3 v/v) are collected, and recrystallization from the methanol gives 400 mg of cholesta-5,7-diene-la, 3/3-diol. 

When the thiiranoradialene sulphoxide 568 was treated with an equimolar amount of 4-substituted 1,2,4-triazoline-3,5-diones 569, the adducts 570 were formed in quantitative yields671 (equation 363). 

An example of a /zctcro-Diels-Alder reaction in SC-CO2 is the cycloaddition of anthracene with 4-phenyl-1,2,4-triazoline-3,5-dione, carried out at 40 °C and at a pressures between 75 and 216 bar [86]. The rate constant increases with decreasing pressure and the highest reactivity was observed at the critical pressure. The value of the rate constant at the critical pressure was higher than that observed in liquid CHCI3 and MeCN at the same temperature. At higher pressures, the rate is slower than that in the polar solvents, which reflects the apolar nature of SC-CO2 as a solvent. 

Triazoline-3,5-diones, 4-substituted-ene reactions with polydienes, 220 properties of modified polymers, 220... 

In 1974, Vogel and his coworkers62) reported the first synthesis of the syn-benzene bisepisulfide 119 and its thermal behavior. The bisepisulfide 119 is thermola-bile and decomposes at 20 °C with a half-life of about 30 min to form benzene and sulfur as final products. When the reaction was carried out in the presence of 4-phenyl-1,2,4-triazoline-3,5-dione (PTD), 119 gave the product 120 which corres-... 

Fig.8A,B Derivatization of Type I pheromones A Z7-12 OAc with dimethyl disulfide (DMDS) and mass spectra of the DMDS adduct B E5,Z7-12 OAc with 4-methyl-1,2,4-triazoline-3,5-dione (MTAD) and mass spectra of the MTAD adduct...

Methyl-3-(tetramethylcyc opropylidene)propene (176), obtained by isomerization of allene 175 with potassium ferr-butoxide, added to 4-phenyl-1,2,4-triazoline-3,5-dione (PTAD, 177) at room temperature to give the Diels-Alder adduct 178 in 46% yield (Scheme 26) [43]. 

Photolysis of the azirines 68 in the presence of DEAZD gives 1,2,4-triazolines (69, R = Et) via cycloaddition to the nitrile ylid.114 The nitrile ylid generated thermally from 70 gives 1,2,4-triazolines (69, R = Me, R1 = R2 = CF3) (Scheme 7).11S The cycloadditions proceed in good yield, and the triazolines 69 are readily converted into aromatic 1,2,4-triazoles. 

Acyl hydrazides are useful precursors for the synthesis of 1,2,4-triazoles. Reaction of acyl hydrazides 149 with imidoylbenzotriazoles 148 in the presence of catalytic amounts of acetic acid under microwave irradiation afforded 3,4,5-trisubstituted triazoles 150 <06JOC9051>. Treatment of A-substituted acetamides with oxalyl chloride generated imidoyl chlorides, which reacted readily with aryl hydrazides to give 3-aryl-5-methyl-4-substituted[ 1,2,4]triazoles <06SC2217>. 5-Methyl triazoles could be further functionalized through a-lithiation and subsequent reaction with electrophiles. ( )-A -(Ethoxymethylene)hydrazinecarboxylic acid methyl ester 152 was applied to the one-pot synthesis of 4-substituted-2,4-dihydro-3//-1,2,4-triazolin-3-ones 153 from readily available primary alkyl and aryl amines 151 <06TL6743>. An efficient synthesis of substituted 1,2,4-triazoles involved condensation of benzoylhydrazides with thioamides under microwave irradiation <06JCR293>. 

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