IP Library Granted Patent US 10,202,386
Granted Patent B2
US 10,202,386 · App. 15/119,772 · Granted Feb 12, 2019

Pyrrolo[3,2-D]pyrimidine derivatives as inducers of human interferon

Inventors: Keith Biggadike (Stevenage, GB); Aurelie Cecile Champigny (Stevenage, GB); Diane Mary Coe (Stevenage, GB); Daniel Terence Tape (Stevenage, GB); Stephen Allan Smith (Stevenage, GB)
Assignee: GlaxoSmithKline Intellectual Property (No. 2) Limited
C07D487/04A61K31/519A61K39/39A61K2039/55511
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Quick Facts
Patent No.
US 10,202,386
App. No.
15/119,772
Granted
Feb 12, 2019
Kind
B2
Abstract

Compounds of formula (I) and salts thereof: wherein R 1 is hydrogen, methyl or —(CH 2 ) 2 OR 3 , R 2 is methyl or —(CH 2 ) 2 OR 4 , or R 1 and R 2 , together with the nitrogen atom to which they are attached, are linked to form a 5- or 6-membered heterocyclyl wherein the 6-membered heterocyclyl is optionally substituted by two hydroxy substituents; R 3 and R 4 are each independently hydrogen or methyl; and n is an integer having a value of 5 or 6, are inducers of human interferon. Compounds which induce human interferon may be useful in the treatment or prevention of various disorders, for example the treatment or prevention of allergic diseases and other inflammatory conditions, for example allergic rhinitis and asthma, infectious diseases and cancer, and may also be useful as vaccine adjuvants.

Claims (34)

1. A compound of formula (I), or a salt thereof:

wherein:

R 1 is hydrogen, methyl or —(CH 2 ) 2 OR 3 ,

R 2 is methyl or —(CH 2 ) 2 OR 4 ,or

R 1 and R 2 , together with the nitrogen atom to which they are attached, are linked to form a 5- or 6-membered heterocyclyl wherein the 6-membered heterocyclyl is optionally substituted by two hydroxy substituents;

R 3 and R 4 are each independently hydrogen or methyl; and

n is an integer having a value of 5 or 6.

2. A compound according to claim 1 , or a salt thereof, wherein R 2 is hydrogen, methyl or —(CH 2 ) 2 OR 3 , and R 2 is methyl or —(CH 2 ) 2 OR 4 .

3. A compound according to claim 1 wherein R 1 and R 2 , together with the nitrogen atom to which they are attached, are linked to form a 5- or 6-membered heterocyclyl wherein the 6-membered heterocyclyl is optionally substituted by two hydroxy substituents.

4. A compound according to claim 1 wherein n is 5.

5. A compound according to claim 1 wherein n is 6.

6. A compound, or a salt thereof, selected from:

2,6-dimethyl-7-(6-(piperidin- 1-yl)hexyl)-5H-pyrrolo[3,2-d]pyrimidin-4-amine;

2,6-dimethyl-7-(5-(pyrrolidin-1-yl)pentyl)-5H-pyrrolo[3,2-d]pyrimidin-4-amine;

2,2′-((5-(4-amino-2,6-dimethyl-5H-pyrrolo[3,2-d]pyrimidin-7-yl)pentyl)azanediyl)diethanol;

2,2′-((6-(4-amino-2,6-dimethyl-5H-pyrrolo[3,2-d]pyrimidin-7-yl)hexyl)azanediyl)diethanol;

2-((6-(4-amino-2,6-dimethyl-5H-pyrrolo[3,2-d]pyrimidin-7-yl)hexyl)(2-methoxyethyl)amino)ethanol;

7-(6-(bis(2-methoxyethyl)amino)hexyl)-2,6-dimethyl-5H-pyrrolo[3,2-d]pyrimidin-4-amine;

2-((6-(4-amino-2,6-dimethyl-5H-pyrrolo[3,2-d]pyrimidin-7-yl)hexyl)amino)ethanol;

(3R,5S)-1-(6-(4-amino-2,6-dimethyl-5H-pyrrolo[3,2-d]pyrimidin-7-yl)hexyl)piperidine-3,5-diol;

(3R,5R)-1-(6-(4-amino-2,6-dimethyl-5H-pyrrolo[3,2-d]pyrimidin-7-yl)hexyl)piperidine-3,5-diol; and

7-(6-(dimethylamino)hexyl)2,6-dimethyl-5H-pyrrolo[3,2-d]pyrimidin-4-amine.

7. A compound according to claim 1 , which is in the form of a pharmaceutically acceptable salt.

8. A compound according to claim 1 , which is in the form of a free base.

9. A pharmaceutical composition comprising a compound as defined in claim 1 , or a pharmaceutically acceptable salt thereof, and one or more pharmaceutically acceptable excipients.

10. A vaccine composition comprising a compound as defined in claim 1 , or a pharmaceutically acceptable salt thereof, and an antigen or antigen composition.

11. A method of treatment of allergic rhinitis, which method comprises administering to a human subject in need thereof, a therapeutically effective amount of a compound as defined in claim 1 , or a pharmaceutically acceptable salt thereof.

12. A method of treatment of asthma, which method comprises administering to a human subject in need thereof, a therapeutically effective amount of a compound as defined in claim 1 , or a pharmaceutically acceptable salt thereof.

13. A compound according to claim 6 , which is in the form of a pharmaceutically acceptable salt.

14. A compound according to claim 6 , which is in the form of a free base.

15. A pharmaceutical composition comprising a compound as defined in claim 6 , or a pharmaceutically acceptable salt thereof, and one or more pharmaceutically acceptable excipients.

16. A vaccine composition comprising a compound as defined in claim 6 , or a pharmaceutically acceptable salt thereof, and an antigen or antigen composition.

17. A method of treatment of allergic rhinitis, which method comprises administering to a human subject in need thereof, a therapeutically effective amount of a compound as defined in claim 6 , or a pharmaceutically acceptable salt thereof.

18. A method of treatment of asthma, which method comprises administering to a human subject in need thereof, a therapeutically effective amount of a compound as defined in claim 6 , or a pharmaceutically acceptable salt thereof.

Assignments (1)
CHANGE OF ADDRESS Recorded Apr 16, 2025
From: GLAXOSMITHKLINE INTELLECTUAL PROPERTY (NO.2) LIMITED
To: GLAXOSMITHKLINE INTELLECTUAL PROPERTY (NO.2) LIMITED
Reel/Frame 070854/0469 →
Continuity (2)
Provisional Application 61942272 · Feb 20, 2014
Related Publication 20170057963A1 · Mar 2, 2017
Cited By (2)
US 12,226,429 US 12,551,499