HCID 22036340, compound → HCID 131723546, compound

Participants

Reaction Steps

The title compound was prepared according to the procedure described in Example 1, Step 2, starting from 2-chloro-3-(2-phenoxyethoxy)quinoxaline (0.65 g, 2.15 mmol): yield 0.44 g (58%) as the free base. A portion of the free base was converted to its hydrochloride salt: mp 123-126° C.; HRMS m/z calcd for C20H22N4O2 (M)+ 350.1743, found 350.1748. Anal. (C20H22N4O2 1.75 HCl. 0.5 H2O) C, H, N.

Provenance & Evidence