4 5 Diidropirazois
Mostrando 1-5 de 5 artigos, teses e dissertações.
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1. Reaction of β-alkoxyvinyl halomethyl ketones with cyanoacetohydrazide
Este trabalho apresenta a síntese de uma série de treze 1-cianoacetil-5-hidroxi-5-halometil-1H-4,5-diidropirazóis a partir da reação de condensação entre cianoacetohidrazida e 4-alcoxi-3-alquen-2-onas [R³C(O)C(R²)=C(R¹)(OR), onde R³ = CF3, CCl3, CHCl2, CO2Et; R² = H, Me; R¹ = H, Me, Et, Pr, Pentil, c-Hexil, Ph, e R = Me, Et]. Reações de desidr
J. Braz. Chem. Soc.. Publicado em: 2008
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2. USE OF MICROWAVE IRRADIATION IN THE SYNTHESIS OF ENONES AND 4,5-DIHYDRO-1H-PYRAZOLES TRIHALOMETHYL-SUBSTITUTED / USO DE ENERGIA MICROONDAS NA SÍNTESE DE ENONAS E DE 4,5-DIIDROPIRAZÓIS TRIALOMETIL-SUBSTITUÍDOS
The solvent-free microwave-assisted regiospecific synthesis of a series of 5-trihalomethyl-4,5-dihydro-1H-pyrazole (7 - 10) from the cyclocondensation of 1,1,1- trihalo-4-alkoxy-3-alken-2-ones (5 - 6),[ CX3COC(R)2=C(R)1OR, where X = Cl, F; R = Me, Et; R2 = H, Me and R1 = H, Me, Et, Pr, iso-Pr, Bu, iso-Bu, tert-Bu, iso - Pen, Ph, 4-Me-Ph, 4-MeO-Ph, 4-NO2-Ph,
Publicado em: 2008
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3. SÍNTESE DE 1H-PIRAZÓIS USANDO IRRADIAÇÃO DE ULTRA-SOM E DE 2-PIRROLONAS DERIVADAS DO ÁCIDO LEVULÍNICO / SYNTHESIS OF 1H-PYRAZOLES BY ULTRASOUND IRRADIATION AND 2-PYRROLONES DERIVATED FROM LEVULINIC ACID
This work describes the synthesis of 4,5-dihydropirazoles through a sonochemical methodology, from the reaction of cyclocondensation of 1,3-diaryl-2-propen-1-ones with aminoguanidine hydrochloride and thiosemicarbazide. These reactions were carried out in ethanol in periods of reduced time concerning to the methods described in the literature. Then, it prese
Publicado em: 2008
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4. β-ENAMINONAS, 5-HIDRÓXI-4,5-DIIDROPIRAZÓIS E 5- HIDRÓXI-4,5-DIIDROISOXAZÓIS HALOMETILSUBSTITUÍDOS: ESTUDO MOLECULAR POR DIFRAÇÃO DE RAIOS-X / β-ENAMINONES, 5-HYDROXY-4,5-DIHYDROPYRAZOLE AND 5-HYDROXY-4,5-DIHYDROISOXAZOLE HALOMETHYL SUBSTITUTED: MOLECULAR STUDY BY X-RAY DIFFRACTOMETRY
The molecular study by X-ray diffraction of β-aminovinyl ketones [R3C(O)CH=C(R1)N(R4R5), onde R3 = CF3, CCl3, CHCl2; R1 = H, Me; R4 = H; R5 = benzyl, Ph, 5-methylisoxazol-3-yl; R4, R5 = -(CH2)4-, -(CH2)2O(CH2)2-], methyl 5- hydroxy-5-trihalomethyl-4,5-dihydro-1H-pyrazole-1-carboxylate [3-(R1), 4-(R2), and 5- (R3) substituted, where R1 = H, Me; R2 = H, M
Publicado em: 2008
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5. Reações de 1,1,1-tricloro-4-metoxi-3-penten-2-ona com hidrazinas monosubstituídas / 1,1,1-trichloro-4-methoxy-3-penten-2-ona reaction with hydrazines
The 1,1,1-trichloro-4-methoxy-3-penten-2-ona (CCl3COCH=CHOMe) reaction with hydrazines series (RNHNH2, where R = H, Me, tert-Bu, Ph, Ph(F)5, Ph-4-NO2, CO2Me e CONH2) yield to the pyrazoles N-substituted and derivatives formation by [3 + 2] ciclocondensations reactions. These compounds formation is regioespecific, it means, termodinamically controled (excepti
Publicado em: 2005