Examples of 'triazolyl' in a sentence
Meaning of "triazolyl"
Triazolyl is a noun used in chemistry to refer to a group or compound containing a triazole ring
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- Any radical derived from a triazole
How to use "triazolyl" in a sentence
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triazolyl
Triazolyl ethanol derivatives as plant growth regulators.
An oxadiazolyl group or a triazolyl group is preferred.
Triazolyl groups are particularly preferred.
Aryl includes but is not limited to pyrazolyl and triazolyl.
Novel triazolyl hydrazide derivatives and process for their preparation.
Y may be an optionally substituted triazolyl.
More preferably Het is triazolyl or triazolyl substituted by oxo.
These rings also include thiazolyl and triazolyl groups.
Among these groups, triazolyl and furanyl groups are preferable.
Suitable examples of the aromatic heterocyclic group in the above substituents include triazolyl and tetrazolyl.
Thereafter adding a triazolyl moiety to the compound 8 to yield and.
In particular, this invention relates to triazolyl alkanols.
Triazolyl alpha - mercaptoacetanilides as inhibitors of HIV reverse transcriptase.
E represents an imidazolyl group or a triazolyl group ;.
Triazolyl alpha - mercaptoacetanildes as inhibitors of HIV reverse transcriptase.
See also
Examples include pyrazolyl, imidazolyl and triazolyl groups.
Triazolyl tropane derivatives as CCR5 modulators.
Is independently selected from the group consisting of, triazolyl and tetrazolyl.
R8 represents a triazolyl group, a pyridyl group or a halogen atom, and A3 represents a halogen atom.
Preferred heteroaryl radicals that may be mentioned include quinolyl, pyridyl, benzothiazolyl and triazolyl radicals.
The pyridinyl, pyrrolyl, thienyl, furanyl, pyrimidinyl or triazolyl groups are more particularly concerned ;.
In one aspect of the invention A is pyrrolyl, pyrazolyl, imidazolyl or triazolyl.
Representative heteroaryls include, for example, imidazolyl, pyridyl, thiazolyl, triazolyl benzimidazolyl, benzothiazolyl, and benzoxazolyl.
In one embodiment X is selected from pyridinyl, imidazolyl, pyrazolyl and triazolyl.
Is independently a 5-membered heterocycle selected from, triazolyl and tetrazolyl in Formula ( IIIa ) ;.
It may be notably a pyrrolidinyl, piperidinyl, piperazinyl, morpholinyl, dihydrofuranyl, tetrahydrofuranyl, imidazolyl or triazolyl group.
EP 032200 discloses certain triazolyl secondary alcohol derivatives useful as plant growth regulators.
More particularly Het is an optionally substituted imidazolyl, oxazolyl, triazolyl or thienyl.
EP 223327 discloses certain triazolyl tertiary alcohol derivatives useful as plant growth regulators.
In certain embodiments of formula I, Rg is triazolyl.
According to the invention, W3 is preferably chosen from the pyrazolyl, imidazolyl, triazolyl and pyrrolyl radicals.
Preferably Ar2 represents optionally substituted phenyl, pyridinyl, thiazolyl, pyrazolyl, pyridazinyl, thienyl, benzofuranyl, naphthyl or triazolyl.
When R9 represents an optionally substituted heteroaryl, typical values include triazolyl and ( methyl ) triazolyl.
Use according to claim 3, wherein the heterocyclic group is pyridyl, oxazolyl, thiazolyl or triazolyl.
Is independently a 5-membered heterocycle selected from, triazolyl and tetrazolyl ;.
Preferred rings include morpholinyl, pyrimidinyl, phenyl, imidazolyl, piperidinyl, tetrahydropyranyl and triazolyl.
Examples of cyclic aromatic radicals include aryl, indolyl, thienyl, furyl, pyrrolyl, triazolyl and tetrazolyl.
In certain particular embodiments, Ring B is an optionally substituted phenyl, imidazolyl, or triazolyl.
In another embodiment, R2 is independently selected from the group consisting of, triazolyl and tetrazolyl.
The present invention features a compound of Formula ( I ) wherein R11 is benzimidazolyl or triazolyl.
More preferably, R3 represents a morpholino or triazolyl moiety.
In one embodiment, Cyc1 preferably represents imidazolyl or triazolyl.
The urea 40 is converted to the compounds of Formula IN vía the triazolyl intermediate 41.
Typically, in these preferred compounds of the invention, R3 represents a morpholino or triazolyl moiety.
Is a 5-membered heteroaryl ring selected from pyrazolyl, triazolyl and pyrrolyl ;.
Alternatively Ar2 represents optionally substituted phenyl, pyridyl, thiazolyl, pyrazolyl, benzofuryl, naphthyl or triazolyl.
Compound ( I ) is preferably a compound wherein A is a triazolyl group ;.
Preferred 5-membered groups are thienyl, thiazolyl, oxadiazolyl, triazolyl.
For example, the heteroaryl group may be furyl, thienyl, thiazolyl, pyrazolyl, triazolyl or tetrazolyl.
Thus, particular preferred Het groups include imidazolyl, methylimidazolyl, phenylimidazolyl, phenyloxazolyl, triazolyl and thienyl.
