Komatsu Y, Minami N
Eisai Tsukuba Research Laboratories, Ibaraki, Japan.
Chem Pharm Bull (Tokyo). 1995 Oct;43(10):1614-6. doi: 10.1248/cpb.43.1614.
Synthesis of a novel dual inhibitor of thromboxane A2 synthetase and 5-lipoxygenase, 5,7-dimethyl-6-hydroxy-2-methylamino-4-(3- pyridylmethyl)benzothiazole (E3040), was accomplished via a new coupling reaction, in which a key intermediate, (3,6-dihydroxy-2,4-dimethylphenyl)-(3-pyridyl)methanol, was easily synthesized in a high yield from 2,6-dimethyl-1,4-benzohydroquinone and 3-pyridinecarboxaldehyde in 6 N hydrochloric acid. The regio isomers of 3-pyridinecarboxaldehyde also gave the corresponding coupling products in high yields.
通过一种新的偶联反应完成了新型血栓素A2合成酶和5-脂氧合酶双重抑制剂5,7-二甲基-6-羟基-2-甲氨基-4-(3-吡啶基甲基)苯并噻唑(E3040)的合成,其中关键中间体(3,6-二羟基-2,4-二甲基苯基)-(3-吡啶基)甲醇由2,6-二甲基-1,4-苯二酚和3-吡啶甲醛在6N盐酸中以高收率轻松合成。3-吡啶甲醛的区域异构体也能以高收率得到相应的偶联产物。