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filingDate 1974-08-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1976-09-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-1449100-A
titleOfInvention Pyrimidine derivatives processes for their preparation and their use in pharmaceutical compositions
abstract 1449100 Pyrimidine derivatives DR KARL THOMAE GmbH 20 Aug 1974 [20 Aug 1973 26 June 1974] 36606/74 Heading C2C The invention comprises compounds of the general formula (wherein R 1 represents an alkoxy group containing 1 to 3 carbon atoms; a morpholino, thiomorpholino, 1-oxidothiomorpholino or 1,1- dioxidothiomorpholino group; or a piperazino group optionally substituted in the 4-position by an alkanoyl or alkenoyl group containing 1 to 4 carbon atoms (which itself is optionally substituted by a methoxy, carboxyl or acetyl group), by an aminocarboxyl group (which is itself optionally substituted by one or two alkyl groups containing from 1 to 4 carbon atoms or by a methoxymethyl group); by a pyridinoyl, salicyloyl or furanoyl group or by an alkylsulphonyl group containing from 1 to 3 carbon atoms; R 2 represents a morpholino, thiomorpholino, 1-oxidothiomorpholino or 1,1-dioxidothiomorpholino group; or a piperazino group optionally substituted in the 4-position by an alkanoyl group containing 1 to 3 carbon atoms which is itself optionally substituted by an acetyl group; R 3 represents a hydrogen, chlorine or bromine atom; or a nitro, cyano, formyl or acetyl group; and R 4 represents a hydrogen, chlorine or bromine atom; a cyano group; an amino group substituted by a cyclohexyl group, by a phenyl group optionally substituted by a chlorine atom or a carboxyl or carbomethoxy group, or by a pyridyl group; a carbalkoxy group containing 2 to 4 carbon atoms; an alkyl group containing 1 to 6 carbon atoms optionally substituted by one or two carbalkoxy groups containing 2 to 4 carbon atoms; a hydroxyl or mercapto group optionally substituted by an allyl group or by an alkyl group containing 1 to 6 carbon atoms; or a 1- oxidothiomorpholino group) and acid addition salts thereof. They may be prepared by reacting a compound of the formula where one or two of the groups X, Y and Z is a leaving group and the other(s) are as defined above for R 1 , R 2 and R 3 , with a compound of formula where A is as defined above for the appropriate group R 1 , R 2 or R 3 . The compounds of the invention may be used as active ingredients in pharmaceutical compositions.
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