发明名称 Ethanolamine derivates, processes for their preparation and pharmaceutical compositions containing them.
摘要 <p>This invention relates to compounds of the general formula (I) &lt;CHEM&gt; and physiologically acceptable salts and solvates thereof where Ar represents &lt;CHEM&gt; where R&lt;3&gt; is a bond or a straight or branched C1-2alkylene group, R&lt;4&gt; is a hydroxy group or a group R&lt;5&gt;NH- where R&lt;5&gt; represents a group CH3SO2-, HCO- or NH2CO-, &lt;CHEM&gt; &lt;CHEM&gt; where R&lt;6&gt; is a chlorine atom or the group F3C-, &lt;CHEM&gt; k represents an integer from 1 to 8, m represents zero or an integer from 2 to 7 and n represents an integer from 2 to 7 with the proviso that the sum total of k, m and n is 4 to 12; R&lt;1&gt; and R&lt;2&gt; each represents a hydrogen atom or a methyl or ethyl group with the proviso that the sum total of carbon atoms in R&lt;1&gt; and R&lt;2&gt; is not more than 2; R&lt;3&gt;&lt;0&gt; represents hydrogen or C1-2alkyl; X represents an oxygen or sulphur atom; and Y and Q may each represent a bond or an oxygen or sulphur atom with the provisos that at least one of Y and Q represents an oxygen or sulphur atom and when Y is a bond m is zero, or when Y represents an oxygen or sulphur atom m is an integer from 2 to 7; P represents a phenyl group otionally substituted by one or more substituents selected from halogen atoms, or the groups C1-3alkyl, C1-3alkoxy, hydroxy, -CH2OH-, -(CH2)2OH, -CO2H, -CO2CH3, -CO2(CH2)2CH3, -R&lt;7&gt;, COR&lt;7&gt;, -NHCOR&lt;8&gt; and -NR&lt;9&gt;SO2R&lt;1&gt;&lt;0&gt;; where R&lt;7&gt; represents an amino, aminoC1-3alkyl, aminoC1-3dialkyl, pyrrolidino, piperidino, hexamethyleneimino, piperazino, N-methylpiperazino or morpholino group; R&lt;8&gt; represents a hydrogen atom or a C1-4alkyl, C1-4alkoxy, phenyl or amino group; R&lt;9&gt; represents a hydrogen atom or a methyl group; R&lt;1&gt;&lt;0&gt; represents a methyl, phenyl, amino or dimethylamino group; or P represents a pyridyl group optionally substituted by one or two substitutents selected from halogen atoms or hydroxy, C1-3alkyl and C1-3alkoxy groups. The compounds have a stimulant action at beta 2-adrenoreceptors and are useful, in particular, in the treatment of diseases associated with reversible airways obstruction such as asthma and chronic bronchitis.</p>
申请公布号 EP0286242(A2) 申请公布日期 1988.10.12
申请号 EP19880302151 申请日期 1988.03.11
申请人 GLAXO GROUP LIMITED 发明人 SKIDMORE, IAN FREDERICK;FINCH, HARRY;MITCHELL, WILLIAM LEONARD;NAYLOR, ALAN;LUNTS, LAWRENCE HENRY;HARTLEY, DAVID
分类号 A61K31/18;A61K31/395;A61K31/135;A61K31/165;A61K31/19;A61K31/44;A61K31/4402;A61K31/4406;A61K31/4418;A61K31/47;A61P1/04;A61P9/00;A61P13/02;A61P15/00;A61P25/24;A61P25/26;A61P27/02;A61P27/14;A61P29/00;A61P37/08;C07D213/30;C07D213/32;C07D213/63;C07D213/65;C07D215/26;C07D295/18 主分类号 A61K31/18
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