反应详情

The title compound was prepared from (4-fluoro-2-nitro-5-pyrrolidin-1-yl-phenyl)-carbamic acid tert.-butyl ester (Example C13) (6.37 g, 20 mmol) by hydrogenation with 10% Pd/C according to the general procedure J (method a). Obtained as a grey solid (5.92 g).