Medicinal Chemistry

To Synthesise Phenytoin from Benzil and Urea – Practical Medicinal Chemistry

AIM: TO SYNTHESISE PHENYTOIN FROM BENZIL AND UREA. REQUIREMENTS:  Chemicals: Benzil, Urea, Sodium hydroxide, Ethanol, Concentrated hydrochloric acid. Apparatus: Round bottom flask (100ml), Reflux condenser, Crystallizing dish (500ml), Heating mantle, Stirrer, Beaker (400ml), Filtering flask with Büchner funnel, Graduated cylinders (100ml and 50ml), Petri dish etc. BACKGROUND: Principle: Base catalysed reaction is used between benzyl […]

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To prepare 6-hydroxy nicotinic acid from coumalic acid – Chemistry Practical

Aim: To prepare 6-Hydroxy nicotinic acid from Coumalic acid. Requirements: Sulphuric acid, coumalic acid, methanol, sodium carbonate, hydrochloric acid, sodium hydroxide. Theory: Methyl coumalate is formed from coumalic acid in the presence of methanol. 6-hydroxy nicotinic acid is formed by reaction between methyl coumalate and ammonia. Reaction Involved: Procedure: 1. Preparation of Methyl coumalate: Place

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To prepare and submit Hexamine from urea – Chemistry Practical

Aim: To prepare and submit Hexamine from urea. Requirements: Porcelain dish, formaldehyde, ammonium hydroxide solution, ethanol,  Theory: Hexamethylenetetramine or methanamine or urotropine is a heterocyclic organic compound with the formula (CH₂)6N4. This white crystalline compound is highly soluble in water and polar organic solvents. Reaction involved: Procedure: Add 7.0 g of 20% ammonium hydroxide solution

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To perform the assay of Metronidazole | Practical Medicinal Chemistry B.Pharm 6th Semester

Aim: To perform the assay of Metronidazole. IUPAC Name: 2-(2-methyl-5-nitro-1H-imidazol-1-yl) ethanolMolecular Formula: C6H9N3O3Mol. Wt.: 171.2.Metronidazole contains not less than 99.0 per cent and not more than 101.0 per cent of C6H9N30, calculated on dried basis.Category: Antiamoebic.Dose: For trichomoniasis, 200 mg thrice daily, for 7 days. For amoebiasis, 400 mg thrice daily, for 5 to 10

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To prepare/synthesize chlorobutanol from acetone

AIM: TO PREPARE AND SUBMIT CHLOROBUTANOL FROM ACETONE. Requirements: Acetone, chloroform, potassium hydroxide, round bottom flask, Glass rod and Beaker. Theory: Chloroform (trichloro-2-methyl-2-propanol) is synthesised by nucleophilic addition of chloroform and acetone. The reaction is base driven by sodium or potassium hydroxide. Procedure: Mix dry acetone (5g) and chloroform (10g) with continued stirring & cool

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To determine physicochemical and toxicity properties of Diazepam using free online services.

Aim: To determine physicochemical and toxicity properties using free online services. Theory:     Bringing a pharmaceutical drug to the market is a long term process that costs sixty-five thousand crores of Indian rupees. One promising approach for improving the efficiency and productivity of early discovery in the pharmaceutical industry and academia is Virtual screenings

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To prepare and submit Sulphanilamide from acetanilide – Practical Medicinal Chemistry

Aim: To prepare and submit Sulphanilamide from acetanilide. Requirements: Beaker, funnel, conical flask, Buchner funnel, acetanilide, chlorosulphonic acid, aqueous ammonia. Theory: For the preparation of sulphanilamide, acetanilide is treated with chlorosulphonic acid, which forms p-acetamidobenzene sulphonyl chloride, which on treatment with ammonia gives p-acetamidobenzene sulphonamide, followed by hydrolysis. Reactions involved: Step-I: Synthesis of p-acetamido benzene

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Steroidal Nomenclature – Medicinal Chemistry B Pharmacy 5th Semester

Steroidal Nomenclature and Structure of Steroids, Stereochemistry Steroidal Chemistry is an important part of syllabi in Medicinal Chemistry II, B Pharmacy 5th semester. In This article you came to know about some important basic concepts of Steroidal Nomenclature. Here we will discuss some common structure and Stereo Chemistry of some important steroids. Gonane, Estrane, Pregnane,

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