Jairo Quiroga - Academia.edu (original) (raw)
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Centre National de la Recherche Scientifique / French National Centre for Scientific Research
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Papers by Jairo Quiroga
Se estudio la formacion de compuestos 2,2,4-trisustituidos dela 2,3-dihidro-1H-1,5- enzodiazepina... more Se estudio la formacion de compuestos 2,2,4-trisustituidos dela 2,3-dihidro-1H-1,5- enzodiazepina en la reaccion de acetofenonascon4,5-dimetil-1,2-fenilendiamina. La estructura de los compuestos sintetizados se determino por medio de analisis espectroscopico (UV-V1S,IR,RMN 'H y espectrometria de masas)
instname:Universidad del Rosario, May 1, 2013
Journal of the Brazilian Chemical Society, 2020
ChemInform, Mar 4, 2008
ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was e... more ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
European Journal of Medicinal Chemistry, 2019
Molecular Diversity, 2017
An efficient route for the synthesis of novel 7-aryl and 7-spiropyrazolo[4[Formula: see text],3[F... more An efficient route for the synthesis of novel 7-aryl and 7-spiropyrazolo[4[Formula: see text],3[Formula: see text]:5,6]pyrido[2,3-d]pyrimidine derivatives is described. These compounds were obtained by a cyclocondensation reaction between pyrazolopyridinediamines 4 and aldehydes 5 or cyclic ketones 6 in the presence of acetic acid as catalyst. This procedure provides the desired compounds in good yields under a simple two-step methodology. The obtained compounds were evaluated as AChE inhibitors and showed weak AChe inhibition with [Formula: see text].
Revista Colombiana de Ciencias Químico-Farmacéuticas, 2017
A partir de 6-amino-3-metil-2-(metiltio)pirimidin-4(3H)-ona, aldehídos aromáticos y benzoquinona,... more A partir de 6-amino-3-metil-2-(metiltio)pirimidin-4(3H)-ona, aldehídos aromáticos y benzoquinona, por medio de una reacción de ciclodeshidratación de Michael asistida por radiación de microondas, se realizó la síntesis y caracterización de la serie de derivados tricomponentes pirimido[4,5-b]quinolínicos, y se evaluó la posible actividad antileishmania. Los nuevos compuestos se caracterizaron por análisis espectroscópico de IR, RMN 1H, RMN 13C y MS.
European journal of medicinal chemistry, Jan 5, 2017
A new series of N-substituted 2-pyrazolines 9a-f, 10a-f, 11a-f, 12a-f and 13a-f were obtained fro... more A new series of N-substituted 2-pyrazolines 9a-f, 10a-f, 11a-f, 12a-f and 13a-f were obtained from the cyclocondensation reaction of [(7-chloroquinolin-4-yl)amino]chalcones 8a-f with hydrazine hydrate and its derivatives. Fourteen of the synthesized compounds including the starting chalcones were selected by US National Cancer Institute (NCI) for testing their anticancer activity against 60 different human cancer cell lines, with the most important GI50 values ranging from 0.28 to 11.7 μM (0.13-6.05 μg/mL) and LC50 values ranging from 2.6 to > 100 μM (1.2 to > 51.7 μg/mL), for chalcones 8a,d and pyrazolines 10c,d. All compounds were assessed for antibacterial activity against wild type and multidrug resistant gram negative and gram positive bacteria, with MIC values ranging from 31.25 to 500 μg/mL. Additionally, the novel compounds were tested for antifungal and antiparasitic properties. Although these compounds showed mild activity against Candida albicans, chalcones 8a and 8...
Acta Crystallogr E Struct Rep, 2001
Monatshefte für Chemie - Chemical Monthly, 2016
Tetrahedron Letters, 2015
Abstract Novel fused pyrrolo[1,2-a]pyrimidines and pyrido[1,2-a]pyrimidine derivatives were prepa... more Abstract Novel fused pyrrolo[1,2-a]pyrimidines and pyrido[1,2-a]pyrimidine derivatives were prepared by a cascade of two cyclization reactions between pyrazolopyridinediamines 4 and ω-chloroketones 5–7 in ethanol as solvent and a catalytic amount of acetic acid. This approach provided the title compounds 8–10 in good yields and under mild simple one-step reaction conditions. The structures of the new compounds were unambiguously established by spectroscopic and analytical techniques.
Acta Crystallographica Section C Crystal Structure Communications, 2009
In the title compound, C(12)H(9)N(3)O(2)S, the thienyl substituent is disordered over two sets of... more In the title compound, C(12)H(9)N(3)O(2)S, the thienyl substituent is disordered over two sets of sites with occupancies of 0.749 (3) and 0.251 (3). A combination of N-H...O, C-H...O and C-H...pi hydrogen bonds links the molecules into bilayers and these bilayers are themselves linked into a continuous structure by pi-pi stacking interactions.
Se estudio la formacion de compuestos 2,2,4-trisustituidos dela 2,3-dihidro-1H-1,5- enzodiazepina... more Se estudio la formacion de compuestos 2,2,4-trisustituidos dela 2,3-dihidro-1H-1,5- enzodiazepina en la reaccion de acetofenonascon4,5-dimetil-1,2-fenilendiamina. La estructura de los compuestos sintetizados se determino por medio de analisis espectroscopico (UV-V1S,IR,RMN 'H y espectrometria de masas)
instname:Universidad del Rosario, May 1, 2013
Journal of the Brazilian Chemical Society, 2020
ChemInform, Mar 4, 2008
ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was e... more ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
European Journal of Medicinal Chemistry, 2019
Molecular Diversity, 2017
An efficient route for the synthesis of novel 7-aryl and 7-spiropyrazolo[4[Formula: see text],3[F... more An efficient route for the synthesis of novel 7-aryl and 7-spiropyrazolo[4[Formula: see text],3[Formula: see text]:5,6]pyrido[2,3-d]pyrimidine derivatives is described. These compounds were obtained by a cyclocondensation reaction between pyrazolopyridinediamines 4 and aldehydes 5 or cyclic ketones 6 in the presence of acetic acid as catalyst. This procedure provides the desired compounds in good yields under a simple two-step methodology. The obtained compounds were evaluated as AChE inhibitors and showed weak AChe inhibition with [Formula: see text].
Revista Colombiana de Ciencias Químico-Farmacéuticas, 2017
A partir de 6-amino-3-metil-2-(metiltio)pirimidin-4(3H)-ona, aldehídos aromáticos y benzoquinona,... more A partir de 6-amino-3-metil-2-(metiltio)pirimidin-4(3H)-ona, aldehídos aromáticos y benzoquinona, por medio de una reacción de ciclodeshidratación de Michael asistida por radiación de microondas, se realizó la síntesis y caracterización de la serie de derivados tricomponentes pirimido[4,5-b]quinolínicos, y se evaluó la posible actividad antileishmania. Los nuevos compuestos se caracterizaron por análisis espectroscópico de IR, RMN 1H, RMN 13C y MS.
European journal of medicinal chemistry, Jan 5, 2017
A new series of N-substituted 2-pyrazolines 9a-f, 10a-f, 11a-f, 12a-f and 13a-f were obtained fro... more A new series of N-substituted 2-pyrazolines 9a-f, 10a-f, 11a-f, 12a-f and 13a-f were obtained from the cyclocondensation reaction of [(7-chloroquinolin-4-yl)amino]chalcones 8a-f with hydrazine hydrate and its derivatives. Fourteen of the synthesized compounds including the starting chalcones were selected by US National Cancer Institute (NCI) for testing their anticancer activity against 60 different human cancer cell lines, with the most important GI50 values ranging from 0.28 to 11.7 μM (0.13-6.05 μg/mL) and LC50 values ranging from 2.6 to > 100 μM (1.2 to > 51.7 μg/mL), for chalcones 8a,d and pyrazolines 10c,d. All compounds were assessed for antibacterial activity against wild type and multidrug resistant gram negative and gram positive bacteria, with MIC values ranging from 31.25 to 500 μg/mL. Additionally, the novel compounds were tested for antifungal and antiparasitic properties. Although these compounds showed mild activity against Candida albicans, chalcones 8a and 8...
Acta Crystallogr E Struct Rep, 2001
Monatshefte für Chemie - Chemical Monthly, 2016
Tetrahedron Letters, 2015
Abstract Novel fused pyrrolo[1,2-a]pyrimidines and pyrido[1,2-a]pyrimidine derivatives were prepa... more Abstract Novel fused pyrrolo[1,2-a]pyrimidines and pyrido[1,2-a]pyrimidine derivatives were prepared by a cascade of two cyclization reactions between pyrazolopyridinediamines 4 and ω-chloroketones 5–7 in ethanol as solvent and a catalytic amount of acetic acid. This approach provided the title compounds 8–10 in good yields and under mild simple one-step reaction conditions. The structures of the new compounds were unambiguously established by spectroscopic and analytical techniques.
Acta Crystallographica Section C Crystal Structure Communications, 2009
In the title compound, C(12)H(9)N(3)O(2)S, the thienyl substituent is disordered over two sets of... more In the title compound, C(12)H(9)N(3)O(2)S, the thienyl substituent is disordered over two sets of sites with occupancies of 0.749 (3) and 0.251 (3). A combination of N-H...O, C-H...O and C-H...pi hydrogen bonds links the molecules into bilayers and these bilayers are themselves linked into a continuous structure by pi-pi stacking interactions.