申请人:Sterling Drug Inc.
公开号:US04699984A1
公开(公告)日:1987-10-13
Shown is the process which comprises heating 4-(2-fluorophenyl)-2,6-dimethyl-3,5-pyridinedicarboxylic acid to produce a mixture of 4-(2-fluorophenyl)-2,6-dimethylpyridine and 2,4-dimethyl-5H-[1]benzopyrano[3,4-c]pyridin-5-one, separating the components of said mixture and nitrating 4-(2-fluorophenyl)-2,6-dimethylpyridine to produce 4-(2-fluoro-5-nitrophenyl)-2,6-dimethylpyridine. Also shown are the 3-step synthesis of 4-(2-fluorophenyl)-2,6-dimethyl-3,5-pyridinedicarboxylic acid from 2-fluorobenzaldehyde and the five step synthesis of 1-ethyl-6-fluoro-1,4-dihydro-7-(2,6-dimethyl-4-pyridinyl)-4-oxo-3-quinolin ecarboxylic acid, a highly potent antibacterial agent, starting with 4-(2-fluoro-5-nitrophenyl)-2,6-dimethylpyridine. Other intermediates shown in said five step synthesis include 3-(2,6-dimethyl-4-pyridinyl)-4-fluorobenzeneamine and diethyl 4-fluoro-3-(2,6-dimethyl-4-pyridinyl)anilinomethylenemalonate.
该过程包括加热4-(2-氟苯基)-2,6-二甲基-3,5-吡啶二甲酸,产生4-(2-氟苯基)-2,6-二甲基吡啶和2,4-二甲基-5H-[1]苯并吡喃[3,4-c]吡啶-5-酮的混合物,分离该混合物的组分并对4-(2-氟苯基)-2,6-二甲基吡啶进行硝化,以产生4-(2-氟-5-硝基苯基)-2,6-二甲基吡啶。还展示了从2-氟苯甲醛合成4-(2-氟苯基)-2,6-二甲基-3,5-吡啶二甲酸的三步合成和从4-(2-氟-5-硝基苯基)-2,6-二甲基吡啶开始的1-乙基-6-氟-1,4-二氢-7-(2,6-二甲基-4-吡啶基)-4-氧-3-喹啉羧酸的五步合成,该化合物是一种高效的抗菌剂。在该五步合成中展示了其他中间体,包括3-(2,6-二甲基-4-吡啶基)-4-氟苯胺和二乙酸二乙酯4-氟-3-(2,6-二甲基-4-吡啶基)苯胺甲基亚甲基丙烯酸酯。