The monoacylation of disulfide (I) with 2-furylcarbonyl chloride (II) by means of 48% HBr in ethanol/water at 80 C gives the monoamide (III), which is then condensed with 2-chloro-6,7-dimethoxyquinazoline-4-amine (IV) in refluxing isoamyl alcohol.
Cystamine (I) was acylated with 2-furoyl chloride (II) in the presence of a catalytic amount of HBr to give amide (III). This was then condensed with chloroquinazoline (IV) in refluxing isoamyl alcohol to yield the title compound.