Examples of 'membered heteroaryl' in a sentence
Meaning of "membered heteroaryl"
membered heteroaryl - a chemical term used to describe a specific type of heterocyclic compound with certain structural characteristics
How to use "membered heteroaryl" in a sentence
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membered heteroaryl
One further example of a five membered heteroaryl group includes thiadiazole.
More preferred heteroaryloxy radicals are " lower heteroaryloxy " radicals having five to six membered heteroaryl radicals.
Examples of 6 membered heteroaryl rings include pyridine, pyrimidine and pyrazine.
A preferred optional substituent for a five membered heteroaryl moiety is methyl.
HAR is a 5 membered heteroaryl ring system selected from.
More preferred heteroaryl radicals include five to six membered heteroaryl radicals.
Preferred 5 to 6 membered heteroaryl groups include pyrazolyl, imidazolyl, pyridinyl, pyrimidinyl or pyrazinyl.
More preferred heteroarylalkoxyalkyl radicals are " lower heteroarylalkoxyalkyl radicals having five to six membered heteroaryl radicals.
It shall be understood that a 5-10 membered heteroaryl includes both monocyclic and bicyclic rings.
More preferred heteroarylthio radicals are " lower heteroarylthio " radicals having five to six membered heteroaryl radicals.
In one embodiment, G may be a 5-6 membered heteroaryl optionally substituted by a halogen.
In one embodiment, the heteroaromatic ring is selected from 5-8 membered heteroaryl rings.
In certain embodiments, Rc is a 5 to 6 membered heteroaryl containing one or two nitrogen heteroatoms.
In another embodiment Ra is an optionally substituted 5-6 membered heteroaryl.
In one embodiment, the 6 membered heteroaryl R1 ring is a pyridinyl or a pyrimidinyl ring.
See also
Preferably, heterocyclyl rings are optionally fused with benzo or 4 to 6 membered heteroaryl or heterocyclyl ring.
R4a is phenyl or five or six membered heteroaryl optionally substituted with up to two R16 ;.
In one embodiment, R5 is an optionally substituted 5 membered heteroaryl.
In another preferred embodiment, R1 is a five membered heteroaryl group or comprises a five-membered heteroaryl group.
In some embodiments, ring A is an optionally substituted 6 membered heteroaryl.
Or A1 is a 5 membered heteroaryl group of the formula.
In some embodiments, ring A is 6 membered heteroaryl.
Ring A is a 6 membered heteroaryl ring having one to three nitrogen atoms ;.
Ring J is preferably a phenyl ring or a 5-6 membered heteroaryl ring.
Preferably A is a 5-6 membered heteroaryl or phenyl, each optionally substituted with one to three Ry.
In some embodiments, Q is a 6 membered heteroaryl.
Examples of 5-8 membered heteroaryl include but are not limited to.
In certain embodiments of compounds of Formula I, B is a fused 5-6 membered heteroaryl ring.
The term " 5 or 6 membered heteroaryl group " denotes, for example furanyl, thiophenyl, pyrrolyl, thiazolyl or pyridinyl.
The compound of Claim 1 wherein R2 is a six membered heteroaryl ring.
The 5 or 6 membered heteroaryl can be substituted with 1 RD.
In other embodiments, the heteroaryl group is between 5-10 membered heteroaryl.
In other embodiments, the 5 or 6 membered heteroaryl is substituted with 1 RD.
In certain embodiments, the heteroaryl group is an unsubstituted 5-14 membered heteroaryl.
In other instances, the 5 or 6 membered heteroaryl is substituted with 1 RD.
In certain embodiments, the heteroaryl group is a substituted 5-14 membered heteroaryl.
When A is a 5 to 6 membered heteroaryl ring, preferably the ring contains 1 or 2 nitrogen atoms.
In some embodiments, the heteroaryl group is between 5-20 membered heteroaryl.
In another embodiment, ring A is a 5-7 membered heteroaryl ring, such as pyridinyl, thienyl or pyrrolyl.
Especially preferable examples of " monocyclic aromatic heterocyclyl " include 5 - or 6 - membered heteroaryl.
Specifically, R ″ is independently an optionally substituted, 5-6 membered heteroaryl group, or an optionally substituted phenyl group.
In certain embodiments, Rf is a 5 or 6 membered heteroaryl.
In yet further embodiments, Y is an optionally substituted 5-6 membered heteroaryl or 5-8 membered heterocyclyl.
More preferably, it is non-fused or fused to a 5 - to 6 - membered heteroaryl or heterocyclyl ring.
In other examples, A is a monocyclic 5-6 membered heteroaryl or heterocyclyl group.
In further embodiments, Y is an optionally substituted 5-10 membered heteroaryl or heterocyclyl.
In one embodiment, R is 5 or 6 membered heteroaryl.
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Examples of using Membered
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Membered rings are strained moieties in organic chemistry
Five and six membered ring sugar
The group will continue as a five membered group
Examples of using Heteroaryl
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The heteroaryl group can be monocyclic or polycyclic
In one embodiment the heteroaryl group is unsubstituted
Heteroaryl includes fused or bridged ring systems
