IP Library Granted Patent US 9,422,299
Granted Patent B2
US 9,422,299 · App. 14/694,228 · Granted Aug 23, 2016

Substituted [1,2,4]triazolo[4,3-a]pyrazines as selective NK-3 receptor antagonists

Inventors: Hamid Hoveyda (Brussels, BE); Guillaume Dutheuil (Vedrin, BE); Graeme Fraser (Bousval, BE)
Assignee: EUROSCREEN SA
C07D487/04
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Quick Facts
Patent No.
US 9,422,299
App. No.
14/694,228
Granted
Aug 23, 2016
Kind
B2
Abstract

Novel compounds of Formula I and their use in therapeutic treatments.

Claims (212)

1. A compound of Formula I:

wherein:

R 1 is H, F or methyl;

R 1′ is H;

R 2 is H, F, Cl or methoxy;

R 2′ is H or F;

R 3 is H, F, Cl, methyl, trifluoromethyl or cyano;

R 4 is methyl, ethyl, n-propyl, hydroxyethyl, methoxyethyl, trifluoromethyl, difluoromethyl or fluoromethyl;

R 5 is methyl, ethyl, methoxymethyl, trifluoromethyl, difluoromethyl, or fluoromethyl;

X 1 is N and X 2 is S or O; or X 1 is S and X 2 is N;

represents a single or a double bond depending on X 1 and X 2 ; and

stands for the (R)-enantiomer or for the racemate of the compound of Formula I.

2. The compound according to claim 1 , having Formula I′:

3. The compound according to claim 1 , having Formula Ia:

wherein:

R 1 is H, F or methyl;

R 1′ is H;

R 2 is H, F, Cl or methoxy;

R 2′ is H or F;

R 3 is H, F, Cl, methyl, trifluoromethyl or cyano;

R 4 is methyl, ethyl, n-propyl, hydroxyethyl, methoxyethyl, trifluoromethyl, difluoromethyl or fluoromethyl;

R 5 is methyl, ethyl, methoxymethyl, trifluoromethyl, difluoromethyl or fluoromethyl; and

stands for the (R)-enantiomer or for the racemate of the compound of Formula Ia.

4. The compound according to claim 1 , having Formula Ia′ or Formula Ia″:

wherein

R 1 is H, F or methyl;

R 1′ is H;

R 2 is H, F, Cl or methoxy;

R 2′ is H or F;

R 3 is H, F, Cl, methyl, trifluoromethyl or cyano;

R 4 is methyl, ethyl, n-propyl, hydroxyethyl, methoxyethyl, trifluoromethyl, difluoromethyl or fluoromethyl;

R 5 is methyl, ethyl, methoxymethyl, trifluoromethyl, difluoromethyl or fluoromethyl.

5. The compound according to claim 1 , having Formula Ia-1:

wherein:

R 3 is H, F, Cl, methyl, trifluoromethyl or cyano;

R 4 is methyl, ethyl, n-propyl, hydroxyethyl, methoxyethyl, trifluoromethyl, difluoromethyl or fluoromethyl;

R 5 is methyl, ethyl, methoxymethyl, trifluoromethyl, difluoromethyl or fluoromethyl; and

stands for the (R)-enantiomer or for the racemate of the compound of Formula Ia-1.

6. The compound according to claim 1 , having Formula Ia-2:

wherein:

R 1 is H, F or methyl;

R 1′ is H;

R 2 is H, F, Cl or methoxy;

R 2′ is H or F;

R 3 is H, F, Cl, methyl, trifluoromethyl or cyano;

R 5 is methyl, ethyl, methoxymethyl, trifluoromethyl, difluoromethyl or fluoromethyl; and

stands for the (R)-enantiomer or for the racemate of the compound of Formula Ia-2.

7. The compound according to claim 1 , having Formula Ia-3:

wherein:

R 1 is H, F or methyl;

R 1′ is H;

R 2 is H, F, Cl or methoxy;

R 2′ is H or F;

R 3 is H, F, Cl, methyl, trifluoromethyl or cyano;

R 4 is methyl, ethyl, n-propyl, hydroxyethyl, methoxyethyl, trifluoromethyl, difluoromethyl or fluoromethyl; and

stands for the (R)-enantiomer or for the racemate of the compound of Formula Ia-3.

8. The compound according to claim 1 , having Formula Ib:

wherein:

R 3 is F;

R 5 is methyl, ethyl, trifluoromethyl, difluoromethyl, or fluoromethyl; and

stands for the (R)-enantiomer or for the racemate of the compound of Formula Ib.

9. The compound according to claim 1 , having Formula Ib′:

wherein

R 3 is F; and

R 5 is methyl, ethyl, trifluoromethyl, difluoromethyl, or fluoromethyl.

10. The compound according to claim 1 , having Formula Ic:

wherein:

R 1 is H, F or methyl;

R 1′ is H;

R 2 is H, F, Cl or methoxy;

R 2′ is H or F;

R 3 is H, F, Cl, methyl, trifluoromethyl or cyano;

R 4 is methyl, ethyl, n-propyl or hydroxyethyl;

R 5 is methyl, ethyl or trifluoromethyl; and

stands for the (R)-enantiomer or for the racemate of the compound of Formula Ic.

11. The compound according to claim 1 , having Formula Ic′:

wherein:

R 1 is H, F or methyl;

R 1′ is H;

R 2 is H, F, Cl or methoxy;

R 2′ is H or F;

R 3 is H, F, Cl, methyl, trifluoromethyl or cyano;

R 4 is methyl, ethyl, n-propyl or hydroxyethyl; and

R 5 is methyl, ethyl or trifluoromethyl.

12. The compound according to claim 1 , selected from the group consisting of:

(R)-(3,4-dichlorophenyl) (8-methyl-3-(3-methyl-1,2,4-thiadiazol-5-yl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)methanone;

(R)-(3-(3-ethyl-1,2,4-thiadiazol-5-yl)-8-methyl-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl) (4-fluorophenyl)methanone;

(R)-(4-chlorophenyl) (8-methyl-3-(3-methyl-1,2,4-thiadiazol-5-yl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)methanone;

(R)-(4-chloro-3-fluorophenyl) (8-methyl-3-(3-methyl-1,2,4-thiadiazol-5-yl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)methanone;

(R)-(4-fluorophenyl) (8-methyl-3-(3-methyl-1,2,4-thiadiazol-5-yl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)methanone;

(R)-(3-chloro-4-fluorophenyl) (8-methyl-3-(3-methyl-1,2,4-thiadiazol-5-yl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)methanone;

(R)-(8-methyl-3-(3-methyl-1,2,4-thiadiazol-5-yl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl) (3,4,5-trifluorophenyl)methanone;

(R)-(8-methyl-3-(3-methyl-1,2,4-thiadiazol-5-yl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl) (2,3,4-trifluorophenyl)methanone;

(R)-(3,4-difluorophenyl) (8-methyl-3-(3-methyl-1,2,4-thiadiazol-5-yl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)methanone;

(R)-(8-methyl-3-(3-methyl-1,2,4-thiadiazol-5-yl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl) (2,3,4,5-tetrafluorophenyl)methanone;

(R)-(4-fluorophenyl) (8-(2-hydroxyethyl)-3-(3-methyl-1,2,4-thiadiazol-5-yl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)methanone;

(4-fluorophenyl) (8-(2-hydroxyethyl)-3-(3-methyl-1,2,4-thiadiazol-5-yl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)methanone;

(R)-(3-(3-ethyl-1,2,4-oxadiazol-5-yl)-8-methyl-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl) (4-fluorophenyl)methanone;

(4-fluorophenyl) (8-methyl-3-(3-methyl-1,2,4-thiadiazol-5-yl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)methanone;

(R)-(3-fluorophenyl) (8-methyl-3-(3-methyl-1,2,4-thiadiazol-5-yl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)methanone;

(R)-(3-chlorophenyl) (8-methyl-3-(3-methyl-1,2,4-thiadiazol-5-yl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)methanone;

(R)-(3,5-difluorophenyl) (8-methyl-3-(3-methyl-1,2,4-thiadiazol-5-yl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)methanone;

(R)-(2,4-difluorophenyl) (8-methyl-3-(3-methyl-1,2,4-thiadiazol-5-yl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)methanone;

(R)-(8-methyl-3-(3-methyl-1,2,4-thiadiazol-5-yl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl) (p-tolyl)methanone;

(R)-(8-methyl-3-(3-methyl-1,2,4-thiadiazol-5-yl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl) (phenyl)methanone;

(R)-(8-methyl-3-(3-methyl-1,2,4-thiadiazol-5-yl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl) (4-(trifluoromethyl)phenyl)methanone;

(R)-(8-ethyl-3-(3-methyl-1,2,4-thiadiazol-5-yl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl) (4-fluorophenyl)methanone;

(8-ethyl-3-(3-methyl-1,2,4-thiadiazol-5-yl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl) (4-fluorophenyl)methanone;

(R)-(4-fluorophenyl) (3-(3-methyl-1,2,4-thiadiazol-5-yl)-8-propyl-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)methanone;

(R)-(4-fluoro-3-methoxyphenyl) (8-methyl-3-(3-methyl-1,2,4-thiadiazol-5-yl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)methanone;

(R)-(8-methyl-3-(3-methyl-1,2,4-thiadiazol-5-yl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl) (o-tolyl)methanone;

(R)-(3-methoxyphenyl) (8-methyl-3-(3-methyl-1,2,4-thiadiazol-5-yl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)methanone;

(R)-(4-fluorophenyl) (8-methyl-3-(3-methyl-1,2,4-oxadiazol-5-yl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)methanone;

(R)-4-(8-methyl-3-(3-methyl-1,2,4-thiadiazol-5-yl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazine-7-carbonyl)benzonitrile;

(8-methyl-3-(3-methyl-1,2,4-thiadiazol-5-yl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl) (2,3,4,5-tetrafluorophenyl)methanone;

(3,4-difluorophenyl) (8-methyl-3-(3-methyl-1,2,4-thiadiazol-5-yl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)methanone;

(8-methyl-3-(3-methyl-1,2,4-thiadiazol-5-yl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl) (2,3,4-trifluorophenyl) methanone;

(8-methyl-3-(3-methyl-1,2,4-thiadiazol-5-yl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl) (3,4,5-trifluorophenyl) methanone;

(3-chloro-4-fluorophenyl) (8-methyl-3-(3-methyl-1,2,4-thiadiazol-5-yl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)methanone;

(4-chloro-3-fluorophenyl) (8-methyl-3-(3-methyl-1,2,4-thiadiazol-5-yl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)methanone;

(4-chlorophenyl) (8-methyl-3-(3-methyl-1,2,4-thiadiazol-5-yl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)methanone;

(3,4-dichlorophenyl) (8-methyl-3-(3-methyl-1,2,4-thiadiazol-5-yl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)methanone;

(3-(3-ethyl-1,2,4-thiadiazol-5-yl)-8-methyl-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl) (4-fluorophenyl)methanone;

(3-(3-ethyl-1,2,4-oxadiazol-5-yl)-8-methyl-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl) (4-fluorophenyl)methanone;

(R)-(4-fluorophenyl) (8-methyl-3-(3-(trifluoromethyl)-1,2,4-thiadiazol-5-yl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)methanone; and

(R)-(3-(3-(difluoromethyl)-1,2,4-thiadiazol-5-yl)-8-methyl-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl) (4-fluorophenyl)methanone.

13. The compound according to claim 12 , selected from the group consisting of:

(R)-(3-(3-ethyl-1,2,4-thiadiazol-5-yl)-8-methyl-5,6-dihydro- [1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl) (4-fluorophenyl)methanone;

(R)-(4-chlorophenyl) (8-methyl-3-(3-methyl-1,2,4-thiadiazol-5-yl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)methanone;

(R)-(4-fluorophenyl) (8-methyl-3-(3-methyl-1,2,4-thiadiazol-5-yl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)methanone;

(4-fluorophenyl) (8-methyl-3-(3-methyl-1,2,4-thiadiazol-5-yl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)methanone; and

(R)-(4-fluorophenyl) (8-methyl-3-(3-methyl-1,2,4-oxadiazol-5-yl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)methanone.

14. The compound according to claim 12 , wherein the compound is (R)-(4-fluorophenyl) (8-methyl-3-(3-methyl-1,2,4-thiadiazol-5-yl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)methanone.

15. A compound of Formula I:

wherein:

R 1 is H, F or methyl;

R 1′ is H;

R 2 is H, F, Cl or methoxy;

R 2′ is H or F;

R 3 is H, F, Cl, methyl, trifluoromethyl or cyano;

R 4 is methyl, ethyl, n-propyl, hydroxyethyl, methoxyethyl, trifluoromethyl, difluoromethyl or fluoromethyl;

R 5 is 1-fluoroethyl, 1,1-difluoroethyl or 2,2,2-trifluoroethyl;

X 1 is N and X 2 is S or O; or X 1 is S and X 2 is N;

represents a single or a double bond depending on X 1 and X 2 ; and

stands for the (R)-enantiomer or for the racemate of the compound of Formula I.

16. The compound according to claim 15 , having Formula Ib:

wherein:

R 3 is F;

R 5 is 1-fluoroethyl, 1,1-difluoroethyl or 2,2,2-trifluoroethyl; and

stands for the (R)-enantiomer or for the racemate of the compound of Formula Ib.

17. The compound according to claim 15 , selected from the group consisting of:

(R)-(3-(3-(1,1-difluoroethyl)-1,2,4-oxadiazol-5-yl)-8-methyl-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl) (4-fluorophenyl)methanone;

(R)-(4-fluorophenyl) (8-methyl-3-(3-(2,2,2-trifluoroethyl)-1,2,4-oxadiazol-5-yl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)methanone; and

((8R)-3-(3-(1-fluoroethyl)-1,2,4-oxadiazol-5-yl)-8-methyl-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl) (4-fluorophenyl)methanone.

18. A pharmaceutical composition comprising a compound of Formula I:

wherein:

R 1 is H, F or methyl;

R 1′ is H;

R 2 is H, F, Cl or methoxy;

R 2′ is H or F;

R 3 is H, F, Cl, methyl, trifluoromethyl or cyano;

R 4 is methyl, ethyl, n-propyl, hydroxyethyl, methoxyethyl, trifluoromethyl, difluoromethyl or fluoromethyl;

R 5 is methyl, ethyl, methoxymethyl, trifluoromethyl, difluoromethyl, or fluoromethyl;

X 1 is N and X 2 is S or O; or X 1 is S and X 2 is N;

represents a single or a double bond depending on X 1 and X 2 ; and

stands for the (R)-enantiomer or for the racemate of the compound of Formula I;

and at least one pharmaceutically acceptable carrier, diluent, excipient and/or adjuvant.

19. A medicament comprising a compound of Formula I:

wherein:

R 1 is H, F or methyl;

R 1′ is H;

R 2 is H, F, Cl or methoxy;

R 2′ is H or F;

R 3 is H, F, Cl, methyl, trifluoromethyl or cyano;

R 4 is methyl, ethyl, n-propyl, hydroxyethyl, methoxyethyl, trifluoromethyl, difluoromethyl or fluoromethyl;

R 5 is 1-fluoroethyl, 1,1-difluoroethyl or 2,2,2-trifluoroethyl;

X 1 is N and X 2 is S or O; or X 1 is S and X 2 is N;

represents a single or a double bond depending on X 1 and X 2 ; and

stands for the (R)-enantiomer or for the racemate of the compound of Formula I.

20. A method for inhibiting neurokinin-3 receptor activity in a patient, comprising the administration to said patient of a pharmaceutically effective amount of a compound of Formula I:

wherein:

R 1 is H, F or methyl;

R 1′ is H;

R 2 is H, F, Cl or methoxy;

R 2′ is H or F;

R 3 is H, F, Cl, methyl, trifluoromethyl or cyano;

R 4 is methyl, ethyl, n-propyl, hydroxyethyl, methoxyethyl, trifluoromethyl, difluoromethyl or fluoromethyl;

R 5 is methyl, ethyl, methoxymethyl, trifluoromethyl, difluoromethyl or fluoromethyl;

X 1 is N and X 2 is S or O; or X 1 is S and X 2 is N;

represents a single or a double bond depending on X 1 and X 2 ; and

stands for the (R)-enantiomer or for the racemate of the compound of Formula I.

21. The method according to claim 20 , wherein the patient suffers from a condition selected from the group consisting of depression, anxiety, psychosis, schizophrenia, psychotic disorders, bipolar disorders, cognitive disorders, Parkinson's disease, Alzheimer's disease, attention deficit hyperactivity disorder, pain, convulsion, obesity, inflammatory diseases, emesis, pre-eclampsia, airway related diseases, urinary incontinence, reproduction disorders, contraception and sex hormone-dependent diseases.

22. The method according to claim 21 , wherein the sex hormone-dependent disease is benign prostatic hyperplasia, prostatic hyperplasia, metastatic prostatic carcinoma, testicular cancer, breast cancer, ovarian cancer, androgen dependent acne, male pattern baldness, endometriosis, abnormal puberty, uterine fibrosis, uterine fibroid tumor, uterine leiomyoma, hormone-dependent cancers, hyperandrogenism, hirsutism, virilization, polycystic ovary syndrome, premenstrual dysphoric disease, HAIR-AN syndrome, ovarian hyperthecosis, other manifestations of high intraovarian androgen concentrations, androgen-producing tumor, menorrhagia or adenomyosis.

23. The method according to claim 22 , wherein the other manifestation of high intraovarian androgen concentration is follicular maturation arrest, atresia, anovulation, dysmenorrhea, dysfunctional uterine bleeding or infertility.

24. The method according to claim 22 , wherein the androgen-producing tumor is virilizing ovarian tumor or virilizing adrenal tumor.

25. The method according to claim 21 , wherein the airway related disease is chronic obstructive pulmonary disease, asthma, airway hyperresponsiveness, bronchoconstriction or cough.

26. The method according to claim 21 , wherein the inflammatory disease is irritable bowel syndrome or an inflammatory bowel disorder.

27. The method according to claim 21 , wherein the compound is (R)-(4-fluorophenyl) (8-methyl-3-(3-methyl-1,2,4-thiadiazol-5-yl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)methanone.

28. The method according to claim 20 , wherein the patient suffers from hot flashes.

29. The method according to claim 28 , wherein the compound is (R)-(4-fluorophenyl) (8-methyl-3-(3-methyl-1,2,4-thiadiazol-5-yl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)methanone.

30. A method for inhibiting neurokinin-3 receptor activity in a patient, comprising the administration to said patient of a pharmaceutically effective amount of a compound of Formula I:

wherein:

R 1 is H, F or methyl;

R 1′ is H;

R 2 is H, F, Cl or methoxy;

R 2′ is H or F;

R 3 is H, F, Cl, methyl, trifluoromethyl or cyano;

R 4 is methyl, ethyl, n-propyl, hydroxyethyl, methoxyethyl, trifluoromethyl, difluoromethyl or fluoromethyl;

R 5 is 1-fluoroethyl, 1,1-difluoroethyl or 2,2,2-trifluoroethyl;

X 1 is N and X 2 is S or O; or X 1 is S and X 2 is N;

represents a single or a double bond depending on X 1 and X 2 ; and

stands for the (R)-enantiomer or for the racemate of the compound of Formula I.

Assignments (6)
CHANGE OF NAME Recorded Jul 7, 2026
From: OGEDA SA
To: OGEDA NV
Reel/Frame 075187/0533 →
CHANGE OF NAME Recorded Jul 7, 2026
From: OGEDA NV
To: OGEDA BV
Reel/Frame 075187/0614 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 7, 2026
From: OGEDA BV
To: ASTELLAS PHARMA INC.
Reel/Frame 075187/0656 →
CHANGE OF NAME Recorded Jul 10, 2017
From: EUROSCREEN SA
To: OGEDA SA
Reel/Frame 043476/0178 →
CHANGE OF NAME Recorded May 12, 2017
From: EUROSCREEN SA
To: OGEDA SA
Reel/Frame 042457/0934 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 30, 2015
From: HOVEYDA, HAMID; DUTHEUIL, GUILLAUME; FRASER, GRAEME
To: EUROSCREEN SA
Reel/Frame 036213/0791 →
Priority Claims (3)
EP 13161863 · Mar 29, 2013 · regional
EP 13193025 · Nov 15, 2013 · regional
EP 14154303 · Feb 7, 2014 · regional
Continuity (2)
Continuation In Part PCTEP2014056367 · Mar 28, 2014
Related Publication 20150232471A1 · Aug 20, 2015