A proton-mediated practical synthesis of McGeachin-type bisaminals from 2-(alkylamino)arenecarbaldehydes
and primary amines is achieved, with trifluoroacetic acid as the proton donor. The
use of a proton, a smallest electrophilic activator, allows previously inviable ortho-substituted anilines and linear and branched aliphatic amines to be viable substrates
for McGeachin bisaminal synthesis. Overcoming the steric and electronic limitations
provides a practical synthetic method. The applications in product derivation and
pharmaceutical molecule modification are also demonstrated.
Key words
bisaminals - bridged azacycles - trifluoroacetic acid - proton - tandem reaction -
iminodibenzodiazocine
