FIELD: chemistry.
SUBSTANCE: invention relates to organic and medical chemistry, namely to compounds of substituted 3-aryl-5-phenyl-3H-1,2,3,4-dithiadiazole-2-oxides of the general formula I, where R=Ph (Ia); R=2-CH3C6H4 (Ib); R=Bn (Ic); R=4-FC6H4 (Id); R=4-NO2C6H4 (If); R=3,5-di-FC6H4 (Ig). Substituted oxides represented by formula (I) are prepared by reacting a substituted N'-arylthiobenzhydrazide with thionyl chloride, followed by isolation of the desired product. To isolate the desired product, the excess thionyl chloride is distilled off under vacuum at 45 °C and the residue was recrystallized from cyclohexane. .
EFFECT: technical result is the preparation of substituted 3-aryl-5-phenyl-3H-1,2,3,4-dithiadiazole-2-oxides, which can be used in medicine as antimicrobial agents, in high yield.
3 cl, 1 dwg, 8 ex, 9 tbl
Title | Year | Author | Number |
---|---|---|---|
METHOD OF PRODUCING SUBSTITUTED CHLORIDES OF 2-[(1Z)-1-(3,5-DIARYL-1,3,4-THIADIAZOL-2(3H)-YLIDENE)METHYL]-3,5-DIARYL-1,3,4-TIADIAZOL-3-IYA | 2017 |
|
RU2637926C1 |
SUBSTITUTED 2-[(1Z)-1-(3,5-DIARYL-1,3,4-THIADIAZOL-2(3H)-YLIDEN)METHYL]-3,5-DIARYL-1,3,4-THIADIAZOL-3-IUM CHLORIDES AND METHOD OF OBTAINING THEREOF | 2014 |
|
RU2571102C1 |
METHOD OF PRODUCING HYDRAZONES OF NITRO-TETRAZOLE-5-CARBALDEHYDE | 2012 |
|
RU2522437C2 |
METHOD FOR PRODUCTION OF 4-ARYL-2,7,9-TRIAZASPIRO[4,5]DECANE-6,8,10-TRIONS | 2016 |
|
RU2635105C1 |
METHOD OF PRODUCING 3-ARYL-1H-BENZO[f]CHROMENE DERIVATIVES | 2014 |
|
RU2597363C2 |
HYDRAZONES OF NITRO TETRAZOLE-5-CARBALDEHYDE WITH ANTIMICROBIAL ACTIVITY | 2015 |
|
RU2594983C1 |
METHOD FOR OBTAINING 1'-ARYLHEXAGYRO-1N-SPIRO[PYRIMIDINE-5,2'-PYRROLYSINE]-2,4,6(1H, 3H, 5H)-TRIONES | 2016 |
|
RU2647240C1 |
METHOD FOR SYNTHESIS OF SULPHONE DERIVATIVES OF 2-NITRO-2-(3-ARYL-1,2,4-OXADIAZOL-5-YL)ETHANE | 2009 |
|
RU2404170C1 |
2-SUBSTITUTED 5-HYDROXYPYRANO[2,3-D][1,3]OXAZINE-4,7-DIONES AND A METHOD FOR PRODUCTION THEREOF | 2019 |
|
RU2705183C1 |
SULPHONIC 2-NITRO-2-(3-ARYL-1,2,4-OXADIAZOLE-5-YL)ETHANE DERIVATIVES EXHIBITING ANTILEPROTIC AND ANTITUBERCULOUS ACTIVITY | 2009 |
|
RU2415845C1 |
Authors
Dates
2018-07-04—Published
2016-12-27—Filed