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1, 2, 4-triazole derivatives and their anti mycobacterial activity

机译:1,2,4-三唑衍生物及其抗分枝杆菌活性

摘要

Invention provides antitubercular compounds selected from propargylated 1,2,3 triazoles of Formula I, wherein, X is sulfur(S) or a sulphone (A), n, m represent independently an integer O or 1, with the provision that when ‘n’ is 1, ‘m’ is 1; R1 is hydrogen; C1-C6 linear or branched alkyl group optionally substituted with aryl group; halogen; or aryl group optionally substituted with —OCH3, halogen, and nitro; R2 and R3 are selected from the group consisting of hydrogen, C1-C6 alkyl optionally substituted with heterocyclic ring of 5 to 6 ring atoms containing one to three hetero atoms selected from oxygen, sulfur, nitrogen, which may be substituted with alkyl, arylalkyl, linear or branched alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, or allyl or propargyl groups consisting of 1 to 6 carbon atoms; Z is C1-C6 alkyl optionally substituted with heterocyclic ring of 1 to 6 ring atoms, containing one to three hetero atoms selected from oxygen, sulfur, nitrogen, which may be substituted with arylalkyl, linear or branched alkenyl, substituted alkenyl, alkynyl, substituted alkynyl allyl or propargyl groups consisting of 1 to 6 carbon atoms; with the provision that when ‘m’ is 1, and ‘n’ is zero; R1 is selected from the group consisting of hydrogen, halogen; C1-C6 linear or branched alkyl group optionally substituted with aryl group or aryl group optionally substituted with —OCH3, halogen, and nitro, R2 and R3 are selected from the group consisting of hydrogen, C1-C6 alkyl optionally substituted with heterocyclic ring of 5 to 6 ring atoms containing one to three hetero atoms selected from oxygen, sulfur, nitrogen, which may be substituted with alkyl, arylalkyl, linear or branched alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, or allyl or propargyl groups consisting of 1 to 6 carbon atoms; Z is selected from the group consisting of halogen, C1-C6 linear or branched alkyl group optionally substituted with heterocyclic ring of 1 to 6 ring atoms, containing one to three hetero atoms selected from oxygen, sulfur, nitrogen, wherein the heterocyclic ring may further be substituted with halogen, alkyl, arylalkyl.
机译:本发明提供了选自式I的炔丙基化的1,2,3三唑的抗结核化合物,其中,X是硫(S)或砜(A),n,m独立地表示整数O或1,条件是当'n '是1,'m'是1; R1是氢;任选地被芳基取代的C1-C6直链或支链烷基;卤素;或任选地被-OCH 3,卤素和硝基取代的芳基; R 2和R 3选自氢,C 1 -C 6烷基,其任选地被5至6个环原子的杂环取代,该杂环原子包含选自氧,硫,氮的1至3个杂原子,其可以被烷基,芳基烷基取代,由1至6个碳原子组成的直链或支链烯基,取代的烯基,炔基,取代的炔基或烯丙基或炔丙基。 Z是任选被1至6个环原子的杂环取代的C 1 -C 6烷基,其含有1-3个选自氧,硫,氮的杂原子,其可以被芳基烷基,直链或支链的烯基,取代的烯基,炔基取代由1至6个碳原子组成的炔基烯丙基或炔丙基;规定当“ m”为1且“ n”为零时; R1选自氢,卤素;任选地被芳基取代的C 1 -C 6直链或支链烷基或任选地被-OCH 3,卤素和硝基取代的芳基,R 2和R 3选自氢,任选地被5个杂环取代的C 1 -C 6烷基。到1-6个含有1-3个选自氧,硫,氮的杂原子的环原子,可以被烷基,芳基烷基,直链或支链的烯基,取代的烯基,炔基,取代的炔基或由1-6组成的烯丙基或炔丙基取代碳原子Z选自卤素,C 1 -C 6直链或支链烷基,其任选地被1至6个环原子的杂环取代,包含1至3个选自氧,硫,氮的杂原子,其中杂环可以进一步被卤素,烷基,芳基烷基取代。

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