发明名称 Deoxyhydantoins, processes for their preparation and pharmaceutical compositions containing them.
摘要 <p>Compounds of the formula (1): &lt;Chemistry id="chema01" num="0001"&gt;&lt;Image id="ia01" he="30" wi="82" file="IMGA0001.TIF" imgContent="chem" imgFormat="TIFF" inline="no" /&gt;&lt;/Chemistry&gt;wherein: &lt;UnorderedLists id="ula01" listStyle="none"&gt;&lt;ListItem&gt;Y is -CH&lt;Sub&gt;2&lt;/Sub&gt;CH&lt;Sub&gt;2&lt;/Sub&gt;-, -CH=CH- or -C=C.&lt;/ListItem&gt;&lt;ListItem&gt;n is 1 to 5;&lt;/ListItem&gt;&lt;ListItem&gt;R, is hydrogen, or CO&lt;Sub&gt;2&lt;/Sub&gt; R, represents an ester group in which the R, moiety contains from 1 to 12 carbon atoms;&lt;/ListItem&gt;&lt;ListItem&gt;R&lt;Sub&gt;2&lt;/Sub&gt; is hydrogen, C&lt;Sub&gt;1-4&lt;/Sub&gt; alkyl, trifluoromethyl, or phenyl;&lt;/ListItem&gt;&lt;ListItem&gt;R&lt;Sub&gt;3&lt;/Sub&gt; is hydroxy or protected hydroxy;&lt;/ListItem&gt;&lt;ListItem&gt;R&lt;Sub&gt;5&lt;/Sub&gt; is hydrogen, C&lt;Sub&gt;1-6&lt;/Sub&gt; alkyl, phenyl or phenyl C&lt;Sub&gt;1-6&lt;/Sub&gt; alkyl, any of which phenyl moieties may be substituted by one or more halogen, trifluoromethyl, C&lt;Sub&gt;1-5&lt;/Sub&gt; alkyl, C&lt;Sub&gt;1-6&lt;/Sub&gt; alkoxy or nitro groups; and&lt;/ListItem&gt;&lt;ListItem&gt;X is CH&lt;Sub&gt;2&lt;/Sub&gt; and&lt;/ListItem&gt;&lt;ListItem&gt;R&lt;Sub&gt;4&lt;/Sub&gt; is C,.&lt;Sub&gt;s&lt;/Sub&gt; alkyl, C&lt;Sub&gt;3-8&lt;/Sub&gt; cycloalkyl-C&lt;Sub&gt;1-6&lt;/Sub&gt; alkyl, phenyl-C&lt;Sub&gt;1-6&lt;/Sub&gt; alkyl or naphthyl-C&lt;Sub&gt;1-6&lt;/Sub&gt; alkyl, any of which groups may have one acyclic carbon-carbon bond interrupted by an oxygen atom; hydrogen, C&lt;Sub&gt;3-8&lt;/Sub&gt; cycloalkyl, phenyl or naphthyl, any of which phenyl of naphthyl moieties in R&lt;Sub&gt;4&lt;/Sub&gt; may be substituted by one or more halogen, trifluoromethyl, C&lt;Sub&gt;1-6&lt;/Sub&gt; alkyl, hydroxy, C&lt;Sub&gt;1-6&lt;/Sub&gt; alkoxy or nitro groups; or R&lt;Sub&gt;2&lt;/Sub&gt; and R&lt;Sub&gt;4&lt;/Sub&gt; taken with the carbon atom to which they are joined represent a C&lt;Sub&gt;5-8&lt;/Sub&gt; cycloalkyl group; or&lt;/ListItem&gt;&lt;ListItem&gt;X is CS and&lt;/ListItem&gt;&lt;ListItem&gt;R&lt;Sub&gt;4&lt;/Sub&gt; is C&lt;Sub&gt;1-9&lt;/Sub&gt; alkyl, C&lt;Sub&gt;3-8&lt;/Sub&gt; cycloalkyl-C&lt;Sub&gt;1-6&lt;/Sub&gt; alkyl, phenyl-C&lt;Sub&gt;1-6&lt;/Sub&gt; alkyl or naphthyl-C&lt;Sub&gt;1-6&lt;/Sub&gt; alkyl, having one acyclic carbon-carbon bond interrupted by an oxygen atom, and in which any phenyl or naphthyl moieties may be substituted by one or more halogen, trifluoromethyl, C&lt;Sub&gt;1-6&lt;/Sub&gt; alkyl, hydroxy, C&lt;Sub&gt;1-6&lt;/Sub&gt; alkoxy or nitro groups; and salts thereof; having similar pharmacological activity to natural prostaglandins, processes for their preparation, intermediates useful in those processes and pharmaceutical compositions containing compounds of the formula (I).&lt;/ListItem&gt;&lt;/UnorderedLists&gt;</p>
申请公布号 EP0004723(A1) 申请公布日期 1979.10.17
申请号 EP19790300442 申请日期 1979.03.21
申请人 BEECHAM GROUP PLC 发明人 WOOTTON, GORDON
分类号 A61K31/415;A61K31/4166;A61P43/00;C07D233/32;C07D233/86;(IPC1-7):07D233/32;61K31/415;07D233/86 主分类号 A61K31/415
代理机构 代理人
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