Course Objective(s):
This course will enable the students to –
Course Outcomes (COs):
Course Outcomes |
Teaching Learning Strategies |
Assessment Strategies |
On completion of this course, the students will be able to- CO101: describe some of the important methods of preparation and properties of aliphatic and aromatic nitro and amino compounds mechanistically. CO102: classify different dyes on the basis of their applications, synthesize and correlate their structure and reactivity CO103: outline mechanisms for reactions involving heterocycles (five and six membered) as starting materials and propose syntheses of heterocycles from the major classes. CO104: classify different types of alkaloids, and terpenoids and discuss their chemistry & medicinal importance CO105: describe the structure and medicinal importance of prescribed antipyretic, analgesics, antibiotics, antimalarials and sulpha drugs. |
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Preparation and important reactions of aliphatic and aromatic nitro compounds
Amines (aliphatic and aromatic)- effect of substituent and solvent on basicity, preparation and properties- Gabriel phthalimide synthesis, Hoffmann bromamide reaction, Carbylamine reaction, Mannich reaction, Hoffmann’s exhaustive methylation, Hofmann-elimination reaction, distinction between 1°, 2° and 3° amines with Hinsberg reagent and nitrous acid, amines as phase transfer catalyst.
Diazonium Salts- preparation and their synthetic applications.
Colour and constitution (electronic concept), classification of dyes, chemistry and synthesis of methyl orange, congo red, malachite green, crystal violet, phenolphthalein, fluorescein, alizarin and indigo.
Classification and nomenclature, structure, aromaticity in 5-numbered and 6-membered rings containing one heteroatom- synthesis, reactions and mechanism of substitution reactions of furan, pyrrole (Paal-Knorr synthesis, Knorr pyrrole synthesis, Hantzsch synthesis), thiophene, pyridine (Hantzsch synthesis), pyrimidine, indole (Fischer indole synthesis and Madelung synthesis), quinoline (Skraup synthesis, Friedlander’s synthesis, Knorr quinoline synthesis, Doebner-Miller synthesis) and isoquinoline (Bischler-Napieralski reaction, Pictet-Spengler reaction, Pomeranz-Fritsch reaction).
Alkaloids- natural occurrence, general structural features, isolation and their physiological action, Emde’s modification, structure elucidation and synthesis of nicotine, medicinal importance of nicotine, hygrine, quinine, morphine, cocaine and reserpine.
Terpenoids- occurrence, classification, isoprene rule, elucidation of structure and synthesis of citral and α- terpineol.
Mechanism of drug action (brief idea), classification, structure and therapeutic uses of-
Antipyretics- paracetamol (with synthesis)
Analgesics- ibuprofen (with synthesis), phenacetin, aspirin
Antimalarials- chloroquine (with synthesis)
Antibiotics- chloramphenicol (with synthesis)
Sulpha drugs (with synthesis)- sulpha pyrimidine, sulpha guanidine, sulphamethazine, sulpha pyridine.
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