Examples of 'pyridyl group' in a sentence
Meaning of "pyridyl group"
pyridyl group: A pyridyl group is a chemical functional group consisting of a six-membered ring with five carbon atoms and one nitrogen atom, commonly found in various organic compounds
How to use "pyridyl group" in a sentence
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pyridyl group
Particularly preferred is a phenyl group or a pyridyl group.
A pyridyl group or a pyridazinyl group is preferred.
Examples thereof are a pyridyl group and a pyrimidyl group.
A pyridyl group and a benzimidazolyl group are particularly preferred.
The compounds are all substituted with a pyridyl group.
For example a pyridyl group substituted by oxo is a pyridone.
Thioamides carrying a pyridyl group.
Ar is a pyridyl group or a phenyl group.
Represents a phenyl or a pyridyl group.
The pyridyl group may have one or more substituents B.
The substituent of phenyl or pyridyl group can be one or more.
Particularly preferred example includes the compounds in which R is a phenyl or a pyridyl group.
Amine resins including those having a pyridyl group are often preferred.
It is particularly preferable that the heterocyclic group of D be a pyridyl group.
Q represents a pyridyl group or a quinolyl group ;.
See also
Groups in the brackets in Z stand for substituent groups for a pyridyl group.
Represents a phenyl group, a pyridyl group or an indolyl group.
In other embodiments, it is an optionally substituted pyridyl group.
As the aromatic group, a phenyl or pyridyl group is particularly preferred.
Of these, pyridyl group and furyl group can be mentioned as preferable groups.
This publication does not disclose or suggest that the pyridyl group may carry any substituents.
A compound having a pyridyl group includes, for example, isonicotinic acid and the like.
An example of a particular value for a heteroaryl group represented by hetAr1 is a pyridyl group.
Examples of the benzene-condensed ring of pyridyl group are quinolyl and isoquinolyl.
Examples of such heterocyclic groups include a furyl, thienyl, thiazolyl or pyridyl group.
Represents a pyridyl group optionally substituted as defined in the general formula ( I ).
In a more preferred aspect of the invention, the heteroaryl group is a pyridyl group.
Or X is a pyridyl group which may have one substituent a mentioned below ;.
The compounds of the present invention are unsubstituted at the 6-position of the pyridyl group.
Or X is a pyridyl group which may have one substituent a defined below ;.
Their position of substitution is the 3-position of the mother cyclic group being a pyridyl group.
In another preferable embodiment, Ring c is a pyridyl group substituted by a halogen atom.
In certain exemplary embodiments, R ' is an optionally substituted phenyl or pyridyl group.
Is a pyridyl group which may have a substituent ( s ).
Further, Arm is preferably a pyridyl group.
Represents a pyridyl group which may have a substituent ( s ).
In another embodiment of the invention, R2 substitutent is an optionally substituted pyridyl group.
Of them, a furyl, thienyl, or pyridyl group is particularly preferable.
Advantageously, the preferred heteroaryl group in the definitions of Y is the pyridyl group.
A compound having a pyridyl group includes, for example, isonicotinic acid.
A sulfonyl hydrazide derivative according to claim 6, wherein L is a substituted or unsubstituted pyridyl group.
R ¹ represents a pyridyl group.
A thiazolone of claim 2 wherein R ₂ is an optionally substituted phenyl or optionally substituted pyridyl group.
Preferably, G is a phenyl group, a pyridyl group or a pyrazyl group.
A compound in accordance with Claim 1 where Het 1 represents a substituted pyridyl group.
The R ² pyridyl group is attached to the pyrrol nitrogen at its 4 or 3 carbon.
Here, the heterocyclic group represented by D is particularly preferably a pyridyl group or a pyrrole group.
R8 represents a triazolyl group, a pyridyl group or a halogen atom, and A3 represents a halogen atom.
M is thus a benzyl group, L is an amide bond and X is a pyridyl group.
Is a pyridyl group and R 2 is a phenyl group, or.
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