Thanks for the quick reply Mitch, anyway, I was thinking along the lines of this:
Seperation of thiodyglycol and gassing with HCl to produce Bis(2-chloroethyl)sulfide,
Then adding methylamine to produce a hybrid between nitrogen mustard one, with it's ethylamine group instead of the sulfide group on Bis(2-chloroethyl)sulfide, and the russian ziakov agent with a methyl group attatched instead of the sulfur group.
My guess is that this compound, most likely bis(2-chloroethyl)methylamide would prove to be an EXTREMELY agressive methylating agent, in a way, the LiALH4 of the methylating agents if you will excuse my somewhat shaky analogy.