Title of article :
Regioselective alkylation reactions of 2,4-diphenyl-3H-1-benzazepine give either 3-alkyl-3H-1-benzazepines or 1-alkyl-1H-1-benzazepines
Author/Authors :
Ko، نويسنده , , Allen and Lam، نويسنده , , Aaron and Li، نويسنده , , Jeffrey and Greer، نويسنده , , Edyta M. and Szalda، نويسنده , , David J. and Karimi، نويسنده , , Sasan and Subramaniam، نويسنده , , Gopal and Ramig، نويسنده , , Keith، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2014
Abstract :
2,4-Diphenyl-3H-1-benzazepine is deprotonated with either LDA or KHMDS. The resulting anion is alkylated with alkyl halides or MeOTs, giving either products of alkylation at C3, or at N, or a mixture of both. The regioselectivity depends on the base, presence of the complexing agent HMPA, and the leaving group of the alkylating agent. Using MeI as alkylating agent gives exclusively the C3-methylated product, while using MeOTs gives exclusively the N-methylated product. The N-alkylated products show evidence of stereodynamic behavior in their NMR spectra.
Keywords :
Stereodynamic , 1-Benzazepine , regioselective , Alkylation
Journal title :
Tetrahedron Letters
Journal title :
Tetrahedron Letters