scholarly journals Structure Modification of Quinine on C-9 Hydroxyl Group via Esterification Reaction

2020 ◽  
Vol 9 (1) ◽  
pp. 32-39
Author(s):  
Teni Ernawati ◽  
◽  
Minarti Minarti ◽  
Puspa Dewi Narrij Lotulung ◽  
◽  
...  

Concept the role played by modified quinine in the asymmetric hydroxyl group inspired studies of modified quinine as chiral organic that lead to drug discovery development. A simple and efficient method for C-9 alkylation and arylation of quinine derivatives was reported. Series quinine derivatives were synthesized through the esterification of the hydroxyl group of quinine. The reaction with various alkyl and aryl carbonyl chloride resulted in the series of ester quinine derivatives. The structure of quinine derivatives was characterized by IR, melting point, UV, 1H NMR, 13C NMR, LCMS.

Molecules ◽  
2018 ◽  
Vol 23 (11) ◽  
pp. 2925 ◽  
Author(s):  
Joshua Gavin ◽  
Joel Annor-Gyamfi ◽  
Richard Bunce

Quinazolin-4(3H)-ones have been prepared in one step from 2-aminobenzamides and orthoesters in the presence of acetic acid. Simple 2-aminobenzamides were easily converted to the heterocycles by refluxing in absolute ethanol with 1.5 equivalents of the orthoester and 2 equivalents of acetic acid for 12–24 h. Ring-substituted and hindered 2-aminobenzamides as well as cases incorporating an additional basic nitrogen required pressure tube conditions with 3 equivalents each of the orthoester and acetic acid in ethanol at 110 °C for 12–72 h. The reaction was tolerant towards functionality on the benzamide and a range of structures was accessible. Workup involved removal of the solvent under vacuum and either recrystallization from ethanol or trituration with ether-pentane. Several 5,6-dihydropyrimidin-4(3H)-ones were also prepared from 3-amino-2,2-dimethylpropionamide. All products were characterized by melting point, FT-IR, 1H-NMR, 13C-NMR, and HRMS.


1970 ◽  
Vol 21 ◽  
pp. 1-7 ◽  
Author(s):  
N. P. Rai ◽  
B. B. Adhikari ◽  
Arjun Paudel ◽  
K. Masuda ◽  
R. D. Mckelvey ◽  
...  

From the flowers of Sarcococca coriacea, a triterpenoic acid, oleanolic acid, a pentahydric sugar alcohol, xylitol along with the mixture of steroidal glycosides, stigmasterol-3-O-β-D-glucopyranoside and β-sitosterol-3-O-β-D-glucopyranoside have been isolated by chromatographic technique. Their structures were established on the basis of IR, 1H-NMR, 13C-NMR, spectral data as well as melting point and Co-TLC comparison with the authentic samples. DOI: 10.3126/jncs.v21i0.214Journal of Nepal Chemical Society Vol.21 2006 p.1-7


2017 ◽  
Vol 18 (02) ◽  
pp. 137-145
Author(s):  
Melindra Mulia

Coumarin has been isolated and characteritated from rind of  Citrus nobilis Lour by maseration methode with methanol. After fractionation by n-hexane and ethyl acetate, collected the phase ethyl acetate which positive of coumarin. From ethyl acetate extract coumarin have been isolated by column chromatography. The isolation results was obtain 2,159 g of pure white needle-shape crystalline with the melting point of 126,2-127,60C. Structure of the isolated coumarine was elucidated by spectroscopic methodes, UV-Vis,13C-NMR, 1H-NMR, 2D-NMR (DEPT/HSQC, COSY, NOESY, HMBC) and IR spectra. Based on the spectra data the isolated coumarine is marmin.


2015 ◽  
Vol 5 (1) ◽  
pp. 40
Author(s):  
Norman Ferdinal

Vol 5 No 1ABSTRACT The research about catechin purification from gambier was purposed to find its solubility properties in various solvent such as in cold water, hot water, hexane, ethyl acetate, and methanol. By knowing its solubility properties, the easiest way to purify the catechin could be gotten which is yielding about 7.33%. Further, the molecular structure has been gotten by determining its melting point and using spectrophotometric measurements such as UV, IR, 1H NMR, 13C NMR. Based on those measurements, d-cathecin structure with a melting point of 175 - 177 ºC was founded. The expected benefit from this research is it could be benefiting the development of gambier purification industry in order to enhancing added value of West Sumatera’s commodities. It would make Western Sumatera gaining stronger bargaining position due to the capability on selling not only on the crude form to abroad. The result of this research has indicated that catechin purification can be performed using an organic solvent and water.  Keywords: Purification, catechin, gambier


2013 ◽  
Vol 67 (4) ◽  
Author(s):  
Muhammad Iqbal ◽  
Imam Baloch ◽  
Musa Baloch

AbstractTwenty acid chlorides, 4-(mono/di-benzyloxy)-4-ketobutanoyl chlorides (Ia–XXa) were synthesised by the reaction of monoesters of succinic acid with thionyl chloride. The product thus obtained (4-benzyloxy-4-ketobutanoyl chlorides) was treated with diethylcadmium to convert it into the corresponding keto-esters (Ib–XXb), the mono/di-benzyl-γ-ketohexanoates, with a good yield. All the compounds thus prepared were characterised by physical, spectroscopic (UV-VIS, IR, 1H NMR, 13C NMR), and mass measurements techniques.


2012 ◽  
Vol 11 (2) ◽  
pp. 109
Author(s):  
Darwati ' ◽  
Husen H Bahti ◽  
Supriyatna ' ◽  
Dachriyanus '

The compound tetraoxygenated xanthone was isolated from the crude extract of the stem bark of Garcinia cowaRoxb. The compound tetraoxygenated xanthone was caried out as yellow crystal with melting point 136-1370C.The structure of this compound was detremined base on spectroscopic methods, including UV, IR, 1H-NMR,13C-NMR 1D and 2D. The compound was found to exhibit cytotoxicity against T47D cell by SRB method


2019 ◽  
Vol 6 (3) ◽  
pp. 248-256 ◽  
Author(s):  
Taybeh Farahmand ◽  
Saeedeh Hashemian ◽  
Ali Shibani

Background: Dihydropyrano [3, 2-c]chromenes and their derivatives have great attention for scientists. They have different activities such as biological properties, spasmolytic, diuretic, anticoagulant, anti-cancer, and anti-anaphylactic activity. For these vary biological activities, chromene derivatives have made significant for further progress in medicinal and organic synthesis studies. So, in view of the importance of chromenes, we aimed to synthesis of 3, 4-dihydropyrano [3, 2-c] chromene derivatives. ZIF@ZnTiO3nanocomposite as organocatalyst was used. Method: An effective and applicable technique was used for preparation of 3, 4-dihydropyrano [3, 2- c] chromene derivatives. Dihydropyrano [c] chromenederivatives were prepared by using ZIF@ZnTiO3compositeas a recyclable catalyst. One-pot three-component reaction of aromatic aldehydes, malononitrile, and 4-hydroxycoumarin was done for synthesis of dihydropyrano [c] chromenederivatives over composite catalyst with excellent yields. The as prepared dihydropyrano [c] chromenederivatives were measured by melting point, FTIR, 1H NMR, and 13C NMR. The nano catalyst could be recycled several times. Result: A novel nano catalyst of MOF containing Mn2+ ions and 2- methyl imidazole (ZIF) and zinctitanate (ZIF@ZnTiO3) composite was prepared. The synthesized organocatalyst was studied for preparation of 3, 4-dihydropyrano [3, 2-c] chromene derivatives. One-pot three-component reaction of aromatic aldehydes, malononitrile, and 4-hydroxycoumarin was done for synthesis of dihydropyrano [c] chromene derivatives over composite catalyst with excellent yields. The reaction was optimized. Conclusion: The organocatalyst composite of consist of ZIF and zinctitanate was prepared. The ZIF@ZnTiO3 was used as catalyst for synthesis of 3, 4-dihydropyrano [3, 2-c] chromene derivatives via one-pot three-component condensations of aromatic aldehydes,malononitrile, and 4 hydroxycoumarin. The results of melting point, FTIR, 1H NMR, 13C NMR also confirmed the formation of high yield of 3, 4-dihydropyrano [3, 2-c] chromene derivatives at short time. The appealing properties of this method are environmentally friendly, mild reaction conditions (low reaction time and high yields of pure products), easy work up and recyclability of reaction catalyst.


2020 ◽  
Vol 32 (7) ◽  
pp. 1713-1718
Author(s):  
Jasim Ali Abdullah ◽  
Muwafaq Ayesh Rabeaa

This article involves synthesis of some heterocyclic compounds from an amine derivative using ecofriendly approach (grinding). The first step involves synthesis of Schiff base from benzaldehyde derivatives (3-hydroxybenzaldehyde and 4-nitrobenzaldehyde) with 4-aminoantipyrine. These compounds were used as precursor for the synthesis of heterocyclic compounds and then synthesized tetrazole, oxazepine oxazepane derivatives from Schiff base with sodium azide, phthalic anhydride, maleic anhydride and succinic anhydride, respectively. The heterocyclic compounds were characterized by TLC, melting point, FTIR, 1H NMR, 13C NMR, GC-mass and HRMS analyses.


2015 ◽  
Vol 1088 ◽  
pp. 367-370
Author(s):  
Yu Ting Liu ◽  
Si Meng Song ◽  
Da Wei Yin

A novel efficient method for the synthesis of 4-amino-5- substituted-1,2,4- triazole -3-thione was developed in which substituted aromatic/aliphatic acids with symmetrical dithiocarbohydrazones were used as starting materials and phosphorus pentachloride was used as catalyst.The structures of these products were confirmed by melting point determination, IR, 1H NMR and elemental analysis. This is a novel and cost-effective synthetic method. In addition, the synthetic method avoids the use of organic solvents and significantly improves reaction yields.


2008 ◽  
Vol 59 (4) ◽  
Author(s):  
Gabriela Laura Almajan ◽  
Stefania Felicia Barbuceanu ◽  
Ioana Saramet ◽  
Mihaela Dinu ◽  
Cristian Vasile Doicin ◽  
...  

5-[4-(4X-phenylsulfonyl)phenyl]-1,3,4-oxadiazole-2-thiols, X=H, Cl, Br, reacted with ethyl chloroacetate to give S-alkylated compounds. Aminomethylation of the thione form of oxadiazoles yielded N(3)-derivatives. All the products have been characterized by elemental analysis, IR, 1H-NMR and 13C-NMR. The plant-growth regulating effects of the title compounds were examined. From the biological activity results, we found that most compounds showed weak stimulatory activities at low concentrations.


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