Substituted pyrrolo[3,2-d]pyrimidin-2,4-diones as A
View Patent ↗Disclosed are novel compounds that are A 2B adenosine receptor antagonists having the following structure: wherein R 1 and R 2 are independently chosen from hydrogen, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted aryl, and optionally substituted heteroaryl, and R 4 is an optionally substituted heteroaryl moiety. The compounds of the invention are useful for treating various disease states, including asthma, chronic obstructive pulmonary disorder, pulmonary inflammation, emphysema, diabetic disorders, inflammatory gastrointestinal tract disorders, immunological/inflammatory disorders, cardiovascular diseases, neurological disorders, and diseases related to angiogenesis.
1. A compound having the structure of the formula (I):
wherein:
R 1 and R 2 are independently chosen from hydrogen, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted aryl, and optionally substituted heteroaryl;
R 3 is chosen from hydrogen, hydroxy, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted aryl, and optionally substituted heteroaryl; and
R 4 is an optionally substituted heteroaryl moiety,
with the proviso that R 4 cannot be an unsubstituted five-membered monocyclic heteroaryl ring containing a single S or O hetero atom.
2. The compound of claim 1 , wherein
R 1 and R 2 are independently hydrogen or optionally substituted lower alkyl;
R 3 is hydrogen or hydroxyl; and
R 4 is an optionally substituted five or six membered monocyclic heteroaryl moiety.
3. The compound of claim 2 , wherein R 4 is an optionally substituted five membered heteroaryl moiety.
4. The compound of claim 3 , wherein R 4 contains at least two heteroatoms selected from the group consisting of nitrogen, oxygen, and sulfur.
5. The compound of claim 4 , wherein R 4 contains at least two nitrogen heteroatoms.
6. The compound of claim 5 , wherein R 4 is an optionally substituted pyrazole moiety.
7. The compound of claim 6 , wherein R 4 is substituted with 1 to 3 substituents independently selected from the group consisting of optionally substituted alkyl, optionally substituted heteroaryl, and optionally substituted aryl moieties.
8. The compound of claim 3 , wherein R 4 is an optionally substituted five membered heteroaryl moiety containing only one heteroatom.
9. The compound of claim 8 , wherein R 4 contains a single N heteroatom and is optionally substituted with 1 to 3 substituents independently selected from the group consisting of optionally substituted alkyl, optionally substituted heteroaryl, and optionally substituted aryl moieties.
10. The compound of claim 2 , wherein R 4 is an optionally substituted six membered heteroaryl moiety.
11. The compound of claim 10 , wherein R 4 is a pyridine moiety optionally substituted with 1 to 3 substituents independently selected from the group consisting of optionally substituted alkyl, optionally substituted heteroaryl, and optionally substituted aryl moieties.
12. The compound of claim 1 , wherein the compound is selected from the group consisting of
8-(1-methyl-1H-pyrrol-2-yl)-1,3-dipropyl-1H-pyrrolo[3,2-d]pyrimidine-2,6-dione;
8-(1-(3-(trifluoromethyl)benzyl)-1H-pyrazol-4-yl)-1,3-dipropyl-1H-pyrrolo[3,2-d]pyrimidine-2,6-dione;
8-(1-benzyl-1H-pyrazol-4-yl)-1,3-dipropyl-1H-pyrrolo[3,2-d]pyrimidine-2,6-dione;
8-(1-benzyl-1H-pyrazol-4-yl)-7-hydroxy-1,3-dipropyl-1H-pyrrolo[3,2-d]pyrimidine-2,6-dione;
8-(1-(3-fluorobenzyl)-1H-pyrazol-4-yl)-1,3-dipropyl-1H-pyrrolo[3,2-d]pyrimidine-2,6-dione;
8-(pyridin-4-yl)-1,3-dipropyl-7-hydroxy-1H-pyrrolo[3,2-d]pyrimidine-2,6-dione;
8-(pyridin-2-yl)-1,3-dipropyl-7-hydroxy-1H-pyrrolo[3,2-d]pyrimidine-2,6-dione;
8-(5-(thiophen-2-yl)isoxazol-3-yl)-1,3-dipropyl-1H-pyrrolo[3,2-d]pyrimidine-2,6-dione;
8-(1-(3-(trifluoromethyl)benzyl)-1H-pyrazol-4-yl)-7-hydroxy-1,3-dipropyl-1H-pyrrolo[3,2-d]pyrimidine-2,6-dione; and
8-(N-hydroxypyridin-4-yl)-1,3-dipropyl-1H-pyrrolo[3,2-d]pyrimidine-2,6-dione.
13. A method of treating a pulmonary disorder selected from asthma and pulmonary fibrosis, comprising administering to a mammal in need thereof a therapeutically effective dose of a compound structure of the Formula (I):
wherein:
R 1 and R 2 are independently chosen from hydrogen, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted aryl, and optionally substituted heteroaryl;
R 3 is chosen from hydrogen, hydroxy, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted aryl, and optionally substituted heteroaryl; and
R 4 is an optionally substituted heteroaryl moiety,
with the proviso that R 4 cannot be an unsubstituted five-membered monocyclic heteroaryl ring containing a single S or O hetero atom.
14. The method of claim 13 , wherein the pulmonary disorder is asthma.
15. The method of claim 13 , wherein the pulmonary disorder is pulmonary fibrosis.
16. A pharmaceutical formulations, comprising a therapeutically effective amount of a therapeutically effective dose of a compound having the structure of the Formula (I):
wherein:
R 1 and R 2 are independently chosen from hydrogen, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted aryl, and optionally substituted heteroaryl;
R 3 is chosen from hydrogen, hydroxy, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted aryl, and optionally substituted heteroaryl; and
R 4 is an optionally substituted heteroaryl moiety,
with the proviso that R 4 cannot be a five-membered monocyclic heteroaryl ring containing a single S or O hetero atom;
and at least one pharmaceutically acceptable excipient.