IP Library Granted Patent US 6,939,895
Granted Patent B2
US 6,939,895 · App. 10/326,713 · Granted Sep 6, 2005

Calcium receptor-active compounds

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Quick Facts
Patent No.
US 6,939,895
App. No.
10/326,713
Granted
Sep 6, 2005
Kind
B2
Abstract

A novel calcium receptor active compound having the formula is provided: Ar 1 —[CR 1 R 2 ] p —X—[CR 3 R 4 ] q —[CR 5 R 6 ]—NR 7 —[CR 8 R 9 ]—Ar 2 wherein: Ar 1 is selected from the group consisting of aryl, heteroaryl, bis(arylmethyl)amino, bis(heteroarylmethyl)amino and arylmethyl(heteroarylmethyl)amino; X is selected from the group consisting of oxygen, sulfur, sulfinyl, sulfonyl, carbonyl and amino; R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 and R 9 are, for example, hydrogen or alkyl; Ar 2 is selected from the group consisting of aryl and heteroaryl; p is an integer of from 0 to 6, inclusive; and, q is an integer of from 0 to 14, inclusive.

Claims (65)

1. A compound having the formula:

Ar 5 —[CHR 16 ] t —W—(CH 2 ) u —CHR 17 —NH—CH(R 18 )—Ar 6

wherein:

Ar 5 is naphthyl, phenyl, indole, carbazole, dibenzofuran, or fluorene, optionally substituted with one or more groups independently selected from the group consisting of unsubstituted lower alkyl, halogen, unsubstituted lower alkoxy, lower alkyl substituted with one or more halogens, lower alkoxy substituted with one or more halogens, nitro, dimethylamino, and unsubstituted phenyl;

Ar 6 is 3-methoxy phenyl or alpha-naphthyl;

t is 1;

u is an integer of from 1 to 11, inclusive;

W is selected from the group consisting of oxygen, sulfur, sulfinyl, sulfonyl, and amino;

R 16 and R 17 are H or unsubstituted lower alkyl;

R 18 is unsubstituted lower alkyl;

or a pharmaceutically acceptable salt or hydrate of said compound;

provided that:

when Ar 6 is 3-methoxy-phenyl, then Ar 5 is not 2-chloro-phenyl; and when t=1, R 16 is unsubstituted lower alkyl, W is amino, u=2, each of R 17 end R 18 is H, and Ar 6 is 3-methoxy-phenyl, then Ar 5 is not 3-methoxyphenyl.

2. The compound, salt or hydrate of claim 1 wherein:

Ar 5 is phenyl, napthyl, or carbazole, optionally substituted with one or more groups independently selected from the group consisting of halogen, lower alkyl, unsubstituted lower alkoxy, and lower alkyl substituted with one or more halogens;

Ar 6 is alpha-napthyl;

R 16 is lower alkyl;

R 17 is hydrogen;

W is amino.

3. A compound according to claim 2 selected from the group consisting of:

or a pharmaceutically acceptable salt or hydrate thereof.

4. A pharmaceutical composition comprising a compound claim 1 .

5. The compound, salt or hydrate of claim 1 wherein:

Ar 5 is phenyl, napthyl, or carbazole, optionally substituted with one or more groups independently selected from the group consisting of halogen, lower alkyl, unsubstituted lower alkoxy, and lower alkyl substituted with one or more halogens;

Ar 6 is alpha-napthyl;

t is 1;

R 16 is lower alkyl;

R 17 is hydrogen;

R 18 is lower alkyl; and

W is amino.

6. A pharmaceutical composition comprising a compound having the formula:

Ar 5 —[CHR 16 ] t —W—(CH 2 ) u —CHR 17 —NH—CH(R 18 )—Ar 6

wherein:

Ar 5 is phenyl, indole, carbazole, dibenzofuran, or fluorene, optionally substituted with one or more groups independently selected from the group consisting of unsubstituted lower alkyl, halogen, unsubstituted lower alkoxy, lower alkyl substituted with one or more halogens, lower alkoxy substituted with one or more halogens, nitro, dimethylamino, and unsubstituted phenyl;

Ar 6 is 3-methoxy phenyl or alpha-naphthyl;

t is 1;

u is an integer of from 1 to 11, inclusive;

W is selected from the group consisting of oxygen, sulfur, sulfinyl, sulfonyl, and amino;

R 16 and R 17 are H or unsubstituted lower alkyl;

R 18 is unsubstituted lower alkyl;

or a pharmaceutically acceptable salt or hydrate of said compound;

in a form suitable for administration to a mammal;

provided that:

when Ar 5 is 3-methoxy-phenyl, then Ar 5 is not 2-chloro-phenyl.

7. The compound, salt or hydrate of claim 1 wherein:

Ar 5 is phenyl, napthyl, or carbazole, optionally substituted with one or more groups independently selected from the group consisting of halogen, lower alkyl, unsubstituted lower alkoxy, and lower alkyl substituted with one or more halogens;

Ar 6 is 3-methoxyphenyl;

t is 1;

R 16 is lower alkyl;

R 17 is hydxogen;

R 18 is lower alkyl; and

W is amino.

8. The compound, salt or hydrate of claim 7 , wherein Ar 5 is phenyl optionally substituted with one or more groups independently selected from the group consisting of halogen, lower alkyl, unsubstituted lower alkoxy, and lower alkyl substituted with one or more halogens.

9. The compound, salt or hydrate of claim 8 , wherein Ar 5 is phenyl optionally substituted with one or more unsubstituted lower alkoxy groups.

10. The compound of claim 7 , having the structure:

11. The compound of claim 10 , in a form suitable for administration to a mammal.

12. A composition comprising a therapeutically effective amount of a compound of claim 1 in a pharmaceutically acceptable carrier.

13. A composition comprising a therapeutically effective amount of a compound of claim 2 in a pharmaceutically acceptable carrier.

14. A composition comprising a therapeutically effective amount of a compound of claim 7 in a pharmaceutically acceptable carrier.

15. A composition comprising a therapeutically effective amount of a compound of claim 3 in a pharmaceutically acceptable carrier.

16. A composition comprising a therapeutically effective amount of the compound of claim 10 in a pharmaceutically acceptable carrier.

17. A compound of claim 3 , in a form suitable for administration to a mammal.

18. A method of treating a patient with hyperparathyroidism, said method comprising administering to said patient an effective amount of a compound of claim 1 .

19. The method of claim 18 , wherein said hyperparathyroidism is primary hyperparathyroidism.

20. The method of claim 18 , wherein said hyperparathyroidism is secondary hyperparathyroidism.

Assignments (1)
CORRECTIVE ASSIGNMENT TO CORRECT THE NATURE OF CONVEYANCE AND ASSIGNOR'S NAME PREVIOUSLY RECORDED ON REEL 022390 FRAME 0234. ASSIGNOR(S) HEREBY CONFIRMS THE CHANGE OF NAME. Recorded May 26, 2021
From: KYOWA HAKKO KOGYO CO., LTD.
To: KYOWA HAKKO KIRIN CO., LTD.
Reel/Frame 056583/0647 →