IP Library Granted Patent US 11,299,497
Granted Patent B2
US 11,299,497 · App. 16/772,536 · Granted Apr 12, 2022

Substituted tetrahydropyran dihydrothienopyrimidines and their use as phosphodiesterase inhibitors

Inventors: Jens Larsen (Ballerup, DK); Simon Feldbaek Nielsen (Ballerup, DK); Peter Andersen (Ballerup, DK)
Assignee: UNION therapeutics A/S
C07D495/04
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 11,299,497
App. No.
16/772,536
Granted
Apr 12, 2022
Kind
B2
Abstract

The present invention relates to novel substituted tetrahydropyran dihydrothienopyrimidines with phosphodiesterase inhibitory activity, and to their use in therapy, and to pharmaceutical compositions comprising the compounds and to methods of treating diseases with the compounds (I).

Claims (43)

1. A compound of general formula (I)

wherein:

R 1 is (C 1 -C 4 )alkyl; and

R 2 is selected from the group consisting of (C 1 -C 4 )alkyl, (C 3 -C 6 )cycloalkyl, bridged (C 3 -C 6 )cycloalkyl, (4-8 membered) heterocycloalkyl, bridged (4-8 membered) heterocycloalkyl, and phenyl; wherein the (C 1 -C 4 )alkyl, (C 3 -C 6 )cycloalkyl, bridged (C 3 -C 6 )cycloalkyl, (4-8 membered) heterocycloalkyl, bridged (4-8 membered) heterocycloalkyl, or phenyl is optionally substituted with one or more substituents independently selected from R 3 ;

R 3 is selected from the group consisting of halogen, —CN, —OH, (C 1 -C 4 )alkyl, halo(C 1 -C 4 )alkyl, hydroxy(C 1 -C 4 )alkyl, (C 1 -C 6 )alkoxy, and halo(C 1 -C 4 )alkyloxy; and

S* is a chiral sulfur atom with (R) stereochemistry;

or a pharmaceutically acceptable salt, enantiomer, mixture of enantiomers, diastereomer, mixture of diastereomers, hydrate or solvate thereof.

2. A compound according to claim 1 , wherein R 1 is methyl.

3. A compound according to claim 1 , wherein R 2 is (C 1 -C 4 )alkyl.

4. A compound according to claim 1 , wherein R 2 is (C 3 -C 6 )cycloalkyl, optionally substituted with one or more substituents independently selected from R 3 .

5. A compound according to claim 1 wherein R 2 is a (4-6 membered) heterocycloalkyl.

6. A compound according to claim 1 selected from the group consisting of:

(i) (5R)—N2-methyl-5-oxido-N4-tetrahydropyran-4-yl-N2-(2-tetrahydropyran-4-ylethyl)-6,7-dihydrothieno[3,2-d]pyrimidin-5-ium-2,4-diamine;

(ii) (5R)—N2-ethyl-5-oxido-N4-tetrahydropyran-4-yl-N2-(2-tetrahydropyran-4-ylethyl)-6,7-dihydrothieno[3,2-d]pyrimidin-5-ium-2,4-diamine;

(iii) N4-tert-butyl-N2-methyl-5-oxido-N2-(2-tetrahydropyran-4-ylethyl)-6,7-dihydrothieno[3,2-d]pyrimidin-5-ium-2,4-diamine;

(iv) N2-methyl-5-oxido-N4-propyl-N2-(2-tetrahydropyran-4-ylethyl)-6,7-dihydrothieno[3,2-d]pyrimidin-5-ium-2,4-diamine;

(v) N4-isopropyl-N2-methyl-5-oxido-N2-(2-tetrahydropyran-4-ylethyl)-6,7-dihydrothieno[3,2-d]pyrimidin-5-ium-2,4-diamine;

(vi) N4-butyl-N2-methyl-5-oxido-N2-(2-tetrahydropyran-4-ylethyl)-6,7-dihydrothieno[3,2-d]pyrimidin-5-ium-2,4-diamine;

(vii) N4-isobutyl-N2-methyl-5-oxido-N2-(2-tetrahydropyran-4-ylethyl)-6,7-dihydrothieno[3,2-d]pyrimidin-5-ium-2,4-diamine;

(viii) N2-methyl-N4-(1-methylcyclobutyl)-5-oxido-N2-(2-tetrahydropyran-4-ylethyl)-6,7-dihydrothieno[3,2-d]pyrimidin-5-ium-2,4-diamine;

(ix) N4-cyclobutyl-N2-methyl-5-oxido-N2-(2-tetrahydropyran-4-ylethyl)-6,7-dihydrothieno[3,2-d]pyrimidin-5-ium-2,4-diamine;

(x) 1-[[2-[methyl(2-tetrahydropyran-4-ylethyl)amino]-5-oxido-6,7-dihydrothieno[3,2-d]pyrimidin-5-ium-4-yl]amino]cyclobutanecarbonitrile;

(xi) 1-[[2-[methyl(2-tetrahydropyran-4-ylethyl)amino]-5-oxido-6,7-dihydrothieno[3,2-d]pyrimidin-5-ium-4-yl]amino]cyclopropanecarbonitrile;

(xii) N2-methyl-N4-[(1S)-1-methylpropyl]-5-oxido-N2-(2-tetrahydropyran-4-ylethyl)-6,7-dihydrothieno[3,2-d]pyrimidin-5-ium-2,4-diamine;

(xiii) N2-methyl-N4-[(1R)-1-methylpropyl]-5-oxido-N2-(2-tetrahydropyran-4-ylethyl)-6,7-dihydrothieno[3,2-d]pyrimidin-5-ium-2,4-diamine;

(xiv) N2-methyl-N4-(1-methylcyclopropyl)-5-oxido-N2-(2-tetrahydropyran-4-ylethyl)-6,7-dihydrothieno[3,2-d]pyrimidin-5-ium-2,4-diamine;

(xv) N2-methyl-N4-(6-oxaspiro[3.3]heptan-2-yl)-5-oxido-N2-(2-tetrahydropyran-4-ylethyl)-6,7-dihydrothieno[3,2-d]pyrimidin-5-ium-2,4-diamine;

(xvi) N4-(3-methoxyphenyl)-N2-methyl-5-oxido-N2-(2-tetrahydropyran-4-ylethyl)-6,7-dihydrothieno[3,2-d]pyrimidin-5-ium-2,4-diamine;

(xvii) N4-cyclohexyl-N2-methyl-5-oxido-N2-(2-tetrahydropyran-4-ylethyl)-6,7-dihydrothieno[3,2-d]pyrimidin-5-ium-2,4-diamine;

(xviii) 2-methyl-2-[[2-[methyl(2-tetrahydropyran-4-ylethyl)amino]-5-oxido-6,7-dihydrothieno[3,2-d]pyrimidin-5-ium-4-yl]amino]propan-1-ol;

(xix) N4-ethyl-N2-methyl-5-oxido-N2-(2-tetrahydropyran-4-ylethyl)-6,7-dihydrothieno[3,2-d]pyrimidin-5-ium-2,4-diamine;

(xx) N4-cyclopentyl-N2-methyl-5-oxido-N2-(2-tetrahydropyran-4-ylethyl)-6,7-dihydrothieno[3,2-d]pyrimidin-5-ium-2,4-diamine;

(xxi) N2-methyl-N4-(oxetan-3-yl)-5-oxido-N2-(2-tetrahydropyran-4-ylethyl)-6,7-dihydrothieno[3,2-d]pyrimidin-5-ium-2,4-diamine;

(xxii) [1-[[2-[methyl(2-tetrahydropyran-4-ylethyl)amino]-5-oxido-6,7-dihydrothieno[3,2-d]pyrimidin-5-ium-4-yl]amino]cyclopentyl]methanol;

(xxiii) [1-[[2-[methyl(2-tetrahydropyran-4-ylethyl)amino]-5-oxido-6,7-dihydrothieno[3,2-d]pyrimidin-5-ium-4-yl]amino]cyclobutyl]methanol;

(xxiv) [1-[[2-[methyl(2-tetrahydropyran-4-ylethyl)amino]-5-oxido-6,7-dihydrothieno[3,2-d]pyrimidin-5-ium-4-yl]amino]cyclopropyl]methanol;

or a pharmaceutically acceptable salt, enantiomer, mixture of enantiomers, diastereomer, mixture of diastereomers, hydrate or solvate thereof.

7. A pharmaceutical composition comprising a compound according to claim 1 and one or more pharmaceutically acceptable vehicles, excipients, or carriers.

8. A method for treatment or alleviation of a disease or a disorder or a condition responsive to PDE4 inhibitory activity, comprising administering to a subject in need thereof a therapeutically effective amount of a compound according to claim 1 .

9. A method of treating or ameliorating one or more dermal diseases, disorders, or conditions, comprising administering to a subject in need thereof a therapeutically effective amount of a compound according to claim 1 .

10. The method according to claim 9 , wherein the dermal disease, disorder, or condition is selected from the group consisting of proliferative and inflammatory skin disorders, dermatitis, atopic dermatitis, seborrheic dermatitis, contact dermatitis, hand dermatitis, psoriasis, psoriasis vulgaris, inverse psoriasis, psoriatic arthritis, spondyloarthritis, epidermal inflammation, alopecia, alopecia areata, rosacea, skin atrophy, steroid induced skin atrophy, photo skin ageing, SAPHO syndrome, acne vulgaris, hidradenitis suppurativa, urticaria, pruritis, and eczema.

11. A method of treating or ameliorating one or more dermal diseases, disorders, or conditions, comprising administering to a subject in need thereof a therapeutically effective amount of a pharmaceutical composition according to claim 7 .

12. The method according to claim 11 , wherein the dermal disease, disorder, or condition is selected from the group consisting of proliferative and inflammatory skin disorders, dermatitis, atopic dermatitis, seborrheic dermatitis, contact dermatitis, hand dermatitis, psoriasis, psoriasis vulgaris, inverse psoriasis, psoriatic arthritis, spondyloarthritis, epidermal inflammation, alopecia, alopecia areata, rosacea, skin atrophy, steroid induced skin atrophy, photo skin ageing, SAPHO syndrome, acne vulgaris, hidradenitis suppurativa, urticaria, pruritis, and eczema.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 2, 2022
From: LEO PHARMA A/S
To: UNION THERAPEUTICS A/S
Reel/Frame 060701/0690 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 7, 2021
From: LEO PHARMA A/S
To: UNION THERAPEUTICS A/S
Reel/Frame 056769/0136 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 20, 2020
From: LARSEN, JENS; NIELSEN, SIMON FELDBAEK; ANDERSEN, PETER
To: LEO PHARMA A/S
Reel/Frame 053549/0957 →
Priority Claims (1)
EP 17207660 · Dec 15, 2017 · regional
Continuity (1)
Related Publication 20200385400A1 · Dec 10, 2020
Cited By (1)
US 12,409,172