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Fused pyrimidine derivatives R 0515 Synthesis, Analgesic, Antiinflammatory, Ulcerogenic Index and Antibacterial Activities of Novel 2-Methylthio-3-substituted-5,6,7,8-tetrahydrobenzo(b)thieno[2,3-d]pyrimidin-4(3H)-ones. -A variety of novel title compounds (IX) (15 examples) is synthesized via an innovative route. Some of them, e.g. (IXb) and (IXc), show more potent analgesic and antiinflammatory activity than the reference standard diclofenac sodium. -(ALAGARSAMY*, V.; MEENA, S.; RAMSESHU, K. V.; SOLOMON, V. R.; THIRUMURUGAN, K.; DHANABAL, K.; MURUGAN, M.; Eur.

A variety of 3-(4-methyl phenyl)-2-substituted amino-3H-quinazolin-4-ones were synthesized by reacting the amino group of 2-hydrazino-3-(4-methyl phenyl)-3H-quinazolin-4-one with a variety of aldehydes and ketones. The starting material 2-hydrazino-3-(4-methyl phenyl)-3H-quinazolin-4-one was synthesized from 4-methyl aniline. The title compounds were investigated for analgesic, anti-inflammatory, and ulcerogenic index activities. While the test compounds exhibited significant activity, compounds Al, A2, and A3 showed more potent analgesic activity and the compound A3 showed more potent anti-inflammatory activity when compared to the reference standard diclofenac sodium. Interestingly, the test compounds showed only mild ulcerogenic potential when compared to aspirin.