SYNTHESIS OF NOVEL MONO-SUBSTITUTED TRIAZINE, CONTAINING A FARMACOPHORIC QUINAZOLINE RING F. A. Zulpanov, 1 B. J. Elmuradov, 1 D. M. Ruziboev, 1 B. A. Sobirov 2 , J. O‘. Muyassarov 3 1 ) S.Yu. Yunusov Institute of the Chemistry of Plant Substances Academy of sciences of the Republic of Uzbekistan st. Mirzo-Ulugbek, 77, 100170 Tashkent e-mail: zulpanovf@gmail.com
2) Mirzo Ulugbek National University of Uzbekistan, Faculty of Chemistry 3) Samarkand State University, University blv. 15, Samarkand 140104, Uzbekistan Triazine derivatives are widely used as weed control agents. Most of them are
selective herbicides. At present, preparations based on metamitron and metribuzin are
approved for use. For a long time, triazines (
atrazine ,
simazine ,
propazine ,
promethrin ,
ametrine , etc.) occupied a leading position in terms of production and use in world
agriculture and were very widely used in our country. Since 2007,
atrazine has not been
included in the list of herbicides recommended for use, but in world practice it is still
used in corn and sorghum crops.
Derivatives of
sim -triazines are characterized by systemic and contact action. The
selectivity of their action is associated with the transformation of chlorine-substituted
into the corresponding hydroxy-substituted compound, which is not toxic to cultivated
plants. The mechanism of herbicidal action of most 1,3,5-triazine derivatives is based
on inhibition of the Hill reaction and blocking of water photolysis.
In the course of our research, we synthesized 6-nitroquinazolin-4-one (
1 ) and
reduced the nitro group with tin(II)-chloride dihydrate (SnCl
2
·2H
2
O) to obtain the
corresponding 6-aminoquinazolin-4-one (