FIELD: chemistry.
SUBSTANCE: invention relates to a novel improved method for synthesis of N-(6-methyl-2,4-dioxo-1,2,3,4-tetrahydro-5-pyrimidine-sulphone)-N'-isonictinoyl hydrazide, which can be used as a substance of medicinal agents for treating and preventing secondary immunodeficiencies, mycobacterial and viral infections, by reacting 6- methyluracil-5-sulphochloride with isonicotinic acid hydraside, characterised by that reaction of 6- methyluracil-5-sulphochloride with isonicotinic acid hydrazide in equimolar ratio takes place in a γ- butyrolacton medium at 90-100°C for 2 hours, followed by purification of the desired product in aqueous ammonium solution at 75-80°C and extraction from the solution at pH 4.5.
EFFECT: method shortens duration the process and increases output of the desired product.
1 cl, 2 ex
Title | Year | Author | Number |
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MEDICINAL AGENT | 2002 |
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IMMUNOTROPIC N, N '-(SULPHONYLDI-1,4-PHENYLENE)BIS[(N",N'"-DIMETHYL)METHYLIMINOMETHANE]1,2,3,4-TETRAHYDRO-6-METHYL-2,4-DIOXO-5-PYRIMIDINESULPHONATE | 2007 |
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RU2357960C1 |
N,N'-(SULFONYLDI-1,4-PHENYLENE)-BIS-(N'',N''-DIMETHYLFORM- -AMIDINE)-1,2,3,4-TETRAHYDRO-6-METHYL-2,4-DIOXO-5-PYRIMIDINE SULFONATE STIMULATING CELLULAR METABOLISM AND SHOWING IMMUNOTROPIC AND ANTIBACTERIAL ACTIVITY | 1997 |
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Authors
Dates
2010-11-27—Published
2009-06-02—Filed