Reaction of 2-hydrazino-3-methyl-3,4-dihydrothieno[2,3-d]pyrimidin-4-one de
rivatives 2a,b with aliphatic acids afforded the thienotriazolopyrimidinone
derivatives 3a-d, with nitrous acid yielded tetrazolothienopyrimidinone de
rivatives 4a,b and with carbon disulphide furnished 3-mercaptothienotriazol
opyrimidinone derivatives 5a,b. Also, 2a,b reacted with aldehydes to afford
the arylhydrazones 6a-f which cyclized into thienotriazolopyrimidinone der
ivatives 7a-f. Furthermore, 2a,b condensed with ethyl acetoacetate and ethy
l cyanoacetate to afford 2-(1-pyrazolyl) derivatives 9a,b and 10a,b, respec
tively. On the other hand, 2-hydrazino derivatives 2a,b condensed with a-ha
lo-ketones to yield thienpyrimidotriazinone derivatives 11a,b and with beta
-diketones, to form 2-(1-pyrazolyl) derivatives 12a-f.