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-chemistry behind the anti-malarial drug
QUININE -chemistry behind the anti-malarial drug
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WHAT IS QUININE? Natural, white crystalline alkaloid
Possesses antipyretic, antimalarial , analgesic and anti-inflammatory properties Bitter taste Stereoisomer of quinidine Possesses 2 major ring systems: aromatic quinoline , bicyclic quinuclidine.
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BIOLOGICAL SOURCES and HISTORY
Cinchona species (Rubiaceae) Obtained from cinchona or peruvian bark First discovered by Quechua of Peru and Bolivia First used antimalarial drug
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CHEMICAL STRUCTURE (R)-(6-Methoxyquinolin-4-yl)((2S,4S,8R)-8-vinylquinuclidin-2-yl)methanol
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CHARACTERISTICS Fluoresces in direct sunlight
Sublimes in vacuum at k. Dissociation constants Pk1=5.07 and pK2=9.7 pH of saturated solution=8.8 Fluoresces with a blue colour especially in sulphuric acid.
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Functional groups It's functional groups are: * alkene * tertiary amine (the quinuclidine bicyclic system) * secondary alcohol * quinoline (an aromatic system, specifically 1- azanaphthalene) * phenolic ether (or perhaps simply an aromatic ether)
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Types of bonds present in quinine
All the bonds present in quinine are covalent bonds.
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R and S forms
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Rabe and kindler process
In 1918 Paul Rabe and Karl Kindler obtained a three step preparation of quinine from d- quinotoxine
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IDENTIFICATION TESTS (a)Colour Tests: 1.Oxygenated Acids : Strong, blue fluorescence in sulphuric acid, acetic acid,etc. 2. Herpathite Test: boiling mixture of quinine(0.3g)+ 7.5ml glacial acetic acid+ 5 drops of conc. H2SO4 in 3ml ethanol(0.9v/v)+3.5 ml of I2 solution(0.01w/v) in ethanol—dark crystals of sulphate of iodoquinine (herpathite) obtained.
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(c) Thalleioquin Test: Br2 water+2-3 ml of weakly acidic solution of quinine salt ml of strong ammonia solution—distinct emerald green colouration. (d) Erythroquinine Test(Rosequin Test): Quinine+ dil. Acetic acid+ freshly prepared Br2 water+ 10% solution of [K4Fe(CN)6]+ conc. NH4OH soln—red colouration.
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USES Flavour in carbonated beverages. Antimalarial agent.
Skeletal muscle relaxant. Used to treat hemorrhoids and varicose veins Oxytocic agent. Prophylactic for flu.
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Derivatives of quinine
Quinine Trihydrate Quinine bisulphate heptahydrate Quinine dihydrochloride Quinine hydrochloride dehydrate Quinine sulphate dehydrate
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Quinine trihydrate It has a melting point of 330 K
It becomes anhydrous at 398 K
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Quinine bisulphate Heptahydrate
It is obtained as bitter crystals Also known as Quinbisan, Dentojel.
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Quinine Dihydrochloride
Also known as quinine dichloride, Quinine bimuriate Slightly soluble in chloroform and very slightly soluble in ether Aqueous solutions are found to be higly acidic with a pH of 2.6
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Quinine Hydrochloride dihydrate
Obtained as silky needles of bitter taste It effloresces on exposure to warm air. Forms anhydrous solution at 373 K.
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Quinine sulphate dihydrate
Also known as Quinsan, Quine and Quinate Its is obtained as dull needles or rods making a light and readily compressible mass. Losses water of crystallization at 383 K. Slightly soluble in ether and chloroform
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Quinine isomer : quinidine
(S)-(6-Methoxyquinolin-4-yl)((2R,4S,8R)-8-vinylquinuclidin-2-yl)methanol
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properties It is optical isomer of quinine
It is a diastereomer of quinidine It is found as white powder or crystals Insoluble in water It melts at 441 K
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uses It is an antiarrhythmic agent
It helps in keeping the heart rate normal for the people with certain heart rhythm disorders.
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….THANK YOU…. DONE BY DHRUVI, RUTVI, SIDDHARTH
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