N,N-Dimethylethylenediamine → 3-(8-Chlorodibenz[b,f][1,4]oxazepin-10(11H)-yl)-4-[[2-(dimethylamino)ethyl]amino]-3-cyclobutene-1,2-dione, hydrochloride

Participants

Reaction Steps

A mixture of the title product of Example 5 (0.73 g), N,N-dimethylethylenediamine (0.225 mL) and dioxane (20 mL) was heated to reflux for 20 minutes. Then, most of the dioxane was removed in vacuo and the residue was stirred in methanol (20 mL) at ambient temperature for 1/2 hour and the precipitated white solid was filtered and discarded. The filtrate was concentrated and the residue was chromatographed on silica gel using 1% each of methanol and triethylamine in ethyl acetate to give the free amine of the title compound as a pale yellow solid. To a solution of this solid in CH2Cl2 (3 mL) was added 7 N HCl in dioxane (1 mL) and the mixture concentrated. To the residue was added excess water and the resulting mixture was freeze dried to give the title compound.

Provenance & Evidence