[1,4-C-13(2),1,4-N-15(2)]butanediamine (1), a key compound in the syntheses
of [5,8-C-13(2),1,4,8-N-15(3)]spermidine (2) and [5,8-C-13(2),1,4,8,12-N-1
5(4)]spermine (3), has been prepared as part of a 6-step process from 1,2-d
ibromoethane using potassium [C-13]cyanide and potassium [N-15]phthalimide.
In the course of the syntheses, it was found that 1,4-dibromobutane was ge
nerated from tetrahydrofuran when bromination using triphenylphosphine and
tetrabromomethane took place. A high-yield preparation of monobenzyloxycarb
onyl (Z) derivative of 1, a precursor for 2, was obtained using a water-sol
uble Z reagent, Z-DSP, in a two-phase system of alkaline solution and chlor
oform. All the steps for 1, 2, and 3, were aimed at minimizing the loss of
stable isotopes.