IP Library Granted Patent US 9,993,476
Granted Patent B2
US 9,993,476 · App. 15/348,545 · Granted Jun 12, 2018

Substituted 5-flouro-1H-pyrazolopyridines and their use

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Quick Facts
Patent No.
US 9,993,476
App. No.
15/348,545
Granted
Jun 12, 2018
Kind
B2
Abstract

The present application relates to novel substituted 5-fluoro-1H-pyrazolopyridines, to processes for their preparation, to their use alone or in combinations for the treatment and/or prophylaxis of diseases, and to their use for producing medicaments for the treatment and/or prophylaxis of diseases, in particular for the treatment and/or prophylaxis of cardiovascular disorders.

Claims (30)

1. A method of treating or preventing one or more of coronary heart disease, systolic or diastolic heart failure, angina pectoris, ischaemias, peripheral and cardiac vascular disorders, kidney failure, renal insufficiency, and increased microalbuminurea, comprising administering a therapeutically effective amount of a compound of formula (I)

in which

R 1 represents hydrogen or (C 1 -C 4 )-alkyl,

where (C 1 -C 4 )-alkyl may be substituted by one or two substituents independently of one another selected from the group consisting of fluorine and trifluoromethyl,

or an N-oxide, salt or salt of an N-oxide thereof to a human or animal in need thereof.

2. The method of claim 1 , wherein in the compound of formula (I)

R 1 represents hydrogen or methyl,

where methyl may be substituted by a trifluoromethyl substituent.

3. The method of claim 1 , wherein the compound of formula (I) is selected from the group consisting of:

methyl {4,6-diamino-2-[5-fluoro-1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl]pyrimidin-5-yl}carbamate

methyl {4,6-diamino-2-[5-fluoro-1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl]pyrimidin-5-yl}methylcarbamate

methyl {4,6-diamino-2-[5-fluoro-1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl]pyrimidin-5-yl}(2,2,2-trifluoroethyl)carbamate

methyl {4,6-diamino-2-[5-fluoro-1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl]pyrimidin-5-yl}carbamate hydrochloride

methyl {4,6-diamino-2-[5-fluoro-1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl]pyrimidin-5-yl}carbamate sulphate

methyl {4,6-diamino-2-[5-fluoro-1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl]pyrimidin-5-yl}carbamate phosphate

methyl {4,6-diamino-2-[5-fluoro-1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl]pyrimidin-5-yl}carbamate mesylate

methyl {4,6-diamino-2-[5-fluoro-1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl]pyrimidin-5-yl}carbamate ethane-1,2-disulphonate

methyl {4,6-diamino-2-[5-fluoro-1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl]pyrimidin-5-yl}carbamate maleate and

methyl {4,6-diamino-2-[5-fluoro-1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl]pyrimidin-5-yl}carbamate nitrate.

4. The method of claim 1 , wherein the compound of formula (I) is:

or an N-oxide, salt, or salt of an N-oxide thereof.

5. The method of claim 1 , wherein the method is for treating angina pectoris.

6. The method of claim 1 , wherein the method is for treating vascular disorders.

7. The method of claim 1 , wherein the method is for treating kidney failure.

8. The method of claim 1 , wherein the method further comprises administering a further active compound that is a cGMP-PDE inhibitor selected from the group consisting of sildenafil, vardenafil and tadalafil.

9. The method of claim 1 , wherein the method further comprises administering a further active compound that is an agent having blood pressure lowering activity selected from the group consisting of losartan, candesartan, valsartan, telmisartan, embusartan, bosentan, darusentan, ambrisentan, sitaxsentan, and spironolactone and eplerenone.

10. The method of claim 1 , wherein the method is for treating coronary heart disease.

11. The method of claim 1 , wherein the method is for treating systolic or diastolic heart failure.

12. The method of claim 1 , wherein the method is for treating renal insufficiency.

13. The method of claim 1 , wherein the method is for treating increased microalbuminurea.

Assignments (5)
CHANGE OF PATENTEE ADDRESS Recorded Feb 8, 2021
From: ADVERIO PHARMA GMBH
To: ADVERIO PHARMA GMBH
Reel/Frame 056907/0570 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 4, 2021
From: FOLLMANN, MARKUS; STASCH, JOHANNES-PETER; REDLICH, GORDEN; ACKERSTAFF, JENS; GRIEBENOW, NILS; KROH, WALTER; KNORR, ANDREAS; BECKER, EVA-MARIA; WUNDER, FRANK; LI, VOLKHART MIN-JIAN; HARTMANN, ELKE; MITTENDORF, JOACHIM; SCHLEMMER, KARL-HEINZ; JAUTELAT, ROLF; BIERER, DONALD
To: BAYER SCHERING PHARMA AKTIENGESELLSCHAFT
Reel/Frame 055151/0491 →
NUNC PRO TUNC ASSIGNMENT Recorded Feb 4, 2021
From: BAYER PHARMA AKTIENGESELLSCHAFT
To: BAYER INTELLECTUAL PROPERTY GMBH
Reel/Frame 055152/0031 →
NUNC PRO TUNC ASSIGNMENT Recorded Feb 4, 2021
From: BAYER INTELLECTUAL PROPERTY GMBH
To: ADVERIO PHARMA GMBH
Reel/Frame 055152/0361 →
CHANGE OF NAME Recorded Feb 4, 2021
From: BAYER SCHERING PHARMA AKTIENGESELLSCHAFT
To: BAYER PHARMA AKTIENGESELLSCHAFT
Reel/Frame 055222/0814 →