摘要 |
The present invention provides a thienopyrimidine compound, represented by the formula [wherein, R<SUP>1 </SUP>is C<SUB>1-4 </SUB>alkyl, R<SUP>2 </SUP>is (1) phenyl optionally having a substituent such as amino, mono C<SUB>1-4 </SUB>alkylamino and di C<SUB>1-4 </SUB>alkylamino, or (2) a heterocyclic group optionally having a substituent such as amino, mono C<SUB>1-4 </SUB>alkylamino and di C<SUB>1-4 </SUB>alkylamino and the like, R<SUP>3 </SUP>is a hydrogen atom or C<SUB>1-4 </SUB>alkyl, R<SUP>4 </SUP>is C<SUB>1-4 </SUB>alkyl optionally having a substituent such as C<SUB>1-4 </SUB>alkoxy-carbonyl, carboxyl, mono C<SUB>1-4 </SUB>alkylamino and N-C<SUB>1-4 </SUB>alkyl-N-C<SUB>7-10 </SUB>aralkylamino and the like] or a salt thereof, which has antagonistic action for gonadotropin-releasing hormone.
|