Regioselective nucleophilic aromatic substitution reactions of 5,7-dinitroquinazoline-4-one and 5,7-dinitroquinazoline-4-thione with methylamine: a mechanistic consideration
Amritpal Singh, Neetu Goel
Abstract
Amritpal Singh, Neetu Goel
Abstract
Thiocarbonyls, similar to carbonyls, are able to provide regioselective control for the attack of amines at the peri -position of 5,7-dinitroquinazoline-4-thione through intramolecular N–H–SC hydrogen bonding.
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Thiocarbonyls, similar to carbonyls, are able to provide regioselective control for the attack of amines at the peri -position of 5,7-dinitroquinazoline-4-thione through intramolecular N–H–SC hydrogen bonding.
Key concepts: Chemistry, Regioselectivity, Intramolecular force, Methylamine, Electrophilic aromatic substitution, Nucleophilic substitution, Substitution reaction, Medicinal chemistry