发明名称 Pyrimidine compounds.
摘要 <p>Compounds of the formula (I) :- &lt;CHEM&gt; (I) and their salts are histamine H2-antagonists, wherein: R&lt;o&gt; is 2-guanidinothiazol-4-yl or a group R&lt;1&gt;R&lt;2&gt;N(CHn-Z- wherein R&lt;1&gt; and R&lt;2&gt; are independently hydrogen, C1-6alkyl, phenyl(C1-6)alkyl, furanyl(C1-6)alkyl, thienyl(C1-6)alkyl, C3-10 cycloalkyl, hydroxy(C2-6)alkyl, or halo(C2-6)alkyl (wherein said hydroxy and halo groups are not substituted on the carbon atom adjacent to the nitrogen atom); or R&lt;1&gt; and R&lt;2&gt; together represent - (CH2)r - wherein r is 4 to 7, to form together with the nitrogen atom to which they are attached a 5-8 membered saturated ring; n is an integer from 1 to 6; Z is 2,5-furanyl, 2,5-thienyl, 2,4-pyridyl wherein the R&lt;1&gt;R&lt;2&gt;N(CH2)n group is in the 4-position, 2,4-thiazolyl wherein the R&lt;1&gt;R&lt;2&gt;N(CH2)n group is in the 2-position, or 1,3- or 1,4-phenylene; m is one; or if Z is pyridyl or phenylene m may also be zero; Y is oxygen, sulphur or methylene; or if Z is furanyl, thienyl or thiazolyl Y may also be a bond; p is two, three or four; q is zero or one; R&lt;3&gt; is hydrogen or C1-6alkyl; and R&lt;4&gt; is hydrogen, optionally substituted C1-6alkyl, C3-10- cycloalkyl, C3-10cycloalkyl(C1-6)alkyl, C2-6alkenyl or C2-6alkynyl,and when q is zero R&lt;4&gt; may also be -(CH2)sB wherein s is 1 to 6 and B is optionally substituted aryl or heteroaryl. &lt;??&gt;Pharmaceutical compositions containing them are described as are processes for their preparation. </p>
申请公布号 EP0180298(A2) 申请公布日期 1986.05.07
申请号 EP19850305902 申请日期 1985.08.20
申请人 SMITH KLINE & FRENCH LABORATORIES LIMITED 发明人 BROWN, THOMAS HENRY;DURANT, GRAHAM JOHN
分类号 C07D239/47;A61K31/505;A61P43/00;C07D239/52;C07D239/54;C07D239/545;C07D401/12;C07D405/12;C07D409/12;C07D417/12;(IPC1-7):C07D239/52 主分类号 C07D239/47
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