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Synthesis of Diuretics Diuretics are drugs that increase urine production, used to treat conditions like hypertension, edema, and heart failure. Here are some common classes and their synthesis routes: 1. Thiazide Diuretics (e.g., Hydrochlorothiazide) Synthesis*: Condensation of *2,4-disulfamoyl-5-chloroaniline with formaldehyde and an aldehyde (e.g., formaldehyde) under acidic conditions, followed by cyclization. *Key step*: Formation of the thiazide ring. 2. Loop Diuretics (e.g., Furosemide) Synthesis*: Reaction of *2,4-dichlorobenzoic acid with *furfurylamine*, followed by sulfonamide formation and carboxylation. *Key step*: Introduction of the sulfonamide group. 3. Potassium-Sparing Diuretics (e.g., Spironolactone) *Synthesis*: Derived from steroidal precursors, involving multiple steps including oxidation, hydrolysis, and cyclization. *Key step*: Formation of the lactone ring. 4. Carbonic Anhydrase Inhibitors (e.g., Acetazolamide) Synthesis*: Reaction of *5-amino-1,3,4-thiadiazole-2-sulfonamide with acetyl chloride. *Key step*: Introduction of the acetamido group. These syntheses involve various organic reactions, including condensation, cyclization, and functional group transformations. Let me know if you'd like more details on a specific diuretic or reaction! #snsinstitutions #snsdesignthinkers #designthinking #snscphs