反应详情

The title compound was prepared from (5-chloro-4-iodo-2-nitro-phenyl)-carbamic acid tert.-butyl ester (Example B1) (399 mg, 1 mmol) and dimethylamine (5.6 N in EtOH, 0.36 mL, 2 mmol) in THF (3 mL) at 65° C. for 18 h in a sealed tube according to the general procedure C. Obtained as a yellow solid (386 mg).