作者:David T. Greenwood、Keith B. Mallion、Alexander H. Todd、Ralph W. Turner
DOI:10.1021/jm00240a009
日期:1975.6
Some 2-aryloxymethyl-2,3,5,6-tetrahydro-1,4-oxazines have been shown to possess marked antidepressant activity. The 1,4-oxazines were synthesized by lithium aluminum hydride reduction of the readily available 6-aryloxymethyl-2,3,5,6-tetrahydro-1,4-oxazin-3-ones. High antidepressant activity was associated with ortho substitution of the 2-phenoxymethyl group and with 1,4-oxazines devoid of 4-substituents
一些2-芳氧基甲基-2,3,5,6-四氢-1,4-恶嗪已显示具有显着的抗抑郁活性。通过氢化铝锂还原易得的6-芳氧基甲基-2,3,5,6-四氢-1,4-恶嗪-3-酮合成1,4-恶嗪。高抗抑郁活性与2-苯氧基甲基的邻位取代和缺乏4-取代基的1,4-恶嗪有关。