FIELD: organic chemistry, chemical technology.
SUBSTANCE: invention describes a method for preparing substituted pyrido[1,2-a][1,3]-benzimidazoles of the general formula:
wherein (1): R is NO2; R1 is hydrogen atom (H); (2): R is CF3; R1 is hydrogen atom (H); (3): R is CN; R1 is hydrogen atom (H); (4): R = R1 is CN that can be used as intermediate compounds in synthesis of fluorescent and biologically active substances. Method involves interaction of 2-nitro-4-R-5R1-halogenbenzene with pyridine and reducing the prepared salt of N-(2-nitro-4-R-5-R1-phenyl)pyridinium wherein interaction of 2-nitro-4-R-5-R1-halogenbenzens with pyridine is carried out at temperature 200C and in the mole ratio 2-nitro-4-R-5-R1-halogenbenzene : pyridine = 1:7 and salt alcoholic solution is subjected for reduction with SnCl2 x 2 HO solution in 3% HCl in the mole ratio N-(2-nitro-4-R-5-R1-phenyl)-pyridinium salt : SnCl2 x 2 H2O = 1:3 at temperature 200C for 0.12 h. Method provides preparing the end product with high yield and purity from available raw at room temperature and for short time interval.
EFFECT: improved preparing method.
2 cl, 2 tbl, 8 ex
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Authors
Dates
2004-12-10—Published
2003-04-24—Filed