Three synthetic routes to 5-substituted 1,3-diazacyclohexane derivatives 1
are reported. The first method involves treatment of 1,3-diaminopropan-2-ol
2 with paraformaldehyde to yield 5-hydroxy-1,3-diazacyclohexane 3. A secon
d method is based on the condensation of 2-bromo-2-nitro-1,3-propanediol wi
th tert-butylamine and formaldehyde to yield 1,3-di-tert-butyl-5-bromo-5-ni
tro-1,3-diazacyclohexane 22. The third method relies on the cycloalkylation
of methylenebisacetamide with 3-chloro-2-chloromethyl-2-propene to provide
5-exomethylene-1,3-diacetyl-1,3-diazacyclohexane 28. Functional group mani
pulations of 3, 22, and 28 provide a number of novel 1,3-diazacyclohexanes
functionalized at the 5-position.