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How are substitution reactions used in drug synthesis?

Substitution reactions are very important in drug synthesis because they allow chemists to replace one atom or group with another to change the drug’s properties. Here’s a simple explanation:


1. Introducing Functional Groups

  • Drugs often need specific functional groups (like –OH, –NH₂, –Cl) to work properly.
  • Example: Replacing a hydrogen with a chlorine or amine can make a molecule more active or more stable.

2. Modifying Drug Activity

  • Substitution reactions can increase potency or reduce side effects.
  • Example: Adding a methyl group (–CH₃) to a drug molecule can improve how it binds to the target.

3. Making Drug Derivatives

  • Chemists often create analogues of a drug by substituting groups to find the best version.
  • Example: Many antibiotics and anti-inflammatory drugs are made by changing one part of the molecule using substitution reactions.

4. Protecting or Activating Parts of Molecules

  • Sometimes a group is substituted temporarily to protect it during synthesis or to activate another part for reaction.

Simple takeaway:
Substitution reactions let chemists add, remove, or swap atoms/groups in a drug molecule to make it more effective, stable, or safe.


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