IP Library Granted Patent US 8,809,304
Granted Patent B2
US 8,809,304 · App. 12/086,419 · Granted Aug 19, 2014

Amine compound and use thereof for medical purposes

Inventors: Masatoshi Kiuchi (Osaka, JP); Kaoru Marukawa (Osaka, JP); Nobutaka Kobayashi (Osaka, JP); Kunio Sugahara (Osaka, JP)
Assignee: Mitsubishi Tanabe Pharma Corporation
C07C255/54C07D319/06C07F9/091C07F9/4056C07F9/6527C07F9/09C07C323/32C07F9/653C07C323/43C07C217/64
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Quick Facts
Patent No.
US 8,809,304
App. No.
12/086,419
Granted
Aug 19, 2014
Kind
B2
Abstract

A novel amine compound represented by the following formula (I), which is superior in immunosuppressive action, rejection suppressive action and the like, and shows reduced side effects such as bradycardia and the like, or a pharmaceutically acceptable acid addition salt thereof, or hydrates thereof, or solvate, as well as a pharmaceutical composition containing this compound and a pharmaceutically acceptable carrier. wherein R is a hydrogen atom or P(═O)(OH) 2 , X is an oxygen atom or a sulfur atom, Y is CH 2 CH 2 or CH═CH, R 1 is cyano or alkyl having a carbon number of 1 to 4 and substituted by a halogen atom(s), R 2 is alkyl having a carbon number of 1 to 4 and optionally substituted by a hydroxyl group(s) or a halogen atom(s), R 3 and R 4 may be the same or different and each is a hydrogen atom or alkyl having a carbon number of 1 to 4, and n is 5-8.

Claims (42)

1. A compound represented by the following formula (I)

or a pharmaceutically acceptable acid addition salt thereof, wherein

R is a hydrogen atom or P(═O)(OH) 2 ,

X is an oxygen atom or a sulfur atom,

Y is CH 2 CH 2 or CH═CH, and wherein

R 1 is cyano,

R 2 is alkyl having a carbon number of 1 to 4 and optionally substituted by a hydroxyl group(s) or a halogen atom(s),

R 3 and R 4 may be the same or different and each is a hydrogen atom or alkyl having a carbon number of 1 to 4, and

n is 5-8, or wherein

R 1 is difluoromethyl or trifluoromethyl,

R 2 is methyl optionally substituted by a hydroxyl group(s) or ethyl optionally substituted by a hydroxyl group(s),

R 3 and R 4 each is a hydrogen atom

and n is 6 or 7.

2. The compound of claim 1 , wherein R 3 and R 4 are each a hydrogen atom, or a pharmaceutically acceptable acid addition salt thereof.

3. The compound of claim 1 , having the following formula (Ia) or (Ib)

or a pharmaceutically acceptable acid addition salt thereof, wherein

R is a hydrogen atom or P(═O)(OH) 2 ,

X is an oxygen atom or a sulfur atom, and wherein

R 1 is cyano, and

R 2 is alkyl having a carbon number of 1 to 4 and optionally substituted by a hydroxyl group(s) or a halogen atom(s), or wherein

R 1 is difluoromethyl or trifluoromethyl, and

R 2 is methyl optionally substituted by a hydroxyl group(s) or ethyl optionally substituted by a hydroxyl group(s).

4. The compound of claim 1 , wherein X is an oxygen atom, or a pharmaceutically acceptable acid addition salt thereof.

5. The compound of claim 1 , wherein Y is CH 2 CH 2 , or a pharmaceutically acceptable acid addition salt thereof.

6. The compound of claim 1 , wherein R 1 is trifluoromethyl, or a pharmaceutically acceptable acid addition salt thereof.

7. The compound of claim 1 , wherein R 2 is methyl optionally substituted by a hydroxyl group(s), or a pharmaceutically acceptable acid addition salt thereof.

8. The compound of claim 1 , wherein R 2 is hydroxymethyl, or a pharmaceutically acceptable acid addition salt thereof.

9. The compound of claim 1 , wherein R is a hydrogen atom, or a pharmaceutically acceptable acid addition salt thereof.

10. The compound of claim 1 , wherein the compound of the formula (I) is any of the following a-e, or a pharmaceutically acceptable acid addition salt thereof

a. 2-amino-2-[2-(4-heptyloxy-3-trifluoromethylphenyl)ethyl]propane-1,3-diol, or a pharmaceutically acceptable acid addition salt thereof

b. (E)-2-amino-2-[2-(4-heptyloxy-3-trifluoromethylphenyl)vinyl]propane-1,3-diol, or a pharmaceutically acceptable acid addition salt thereof

c. 2-amino-4-(4-heptyloxy-3-trifluoromethylphenyl)-2-methylbutanol, or a pharmaceutically acceptable acid addition salt thereof

d. (R)-2-amino-4-(4-heptyloxy-3-trifluoromethylphenyl)-2-methylbutanol, or a pharmaceutically acceptable acid addition salt thereof

e. 2-amino-2-[2-(3-cyano-4-heptyloxyphenyl)ethyl]propane-1,3-diol, or a pharmaceutically acceptable acid addition salt thereof.

11. The compound of claim 1 , wherein the compound of the formula (I) is any of the following f-j, or a pharmaceutically acceptable acid addition salt thereof

f. 2-amino-4-(4-heptyloxy-3 -trifluoromethylphenyl)-2-(phosphoryloxymethyl)butanol, or a pharmaceutically acceptable acid addition salt thereof

g. (E)-2-amino-4-(4-heptyloxy-3-trifluoromethylphenyl)-2-(phosphoryloxymethyl)-3-buten- 1 -ol, or a pharmaceutically acceptable acid addition salt thereof

h. phosphoric acid mono[2-amino-4-(4-heptyloxy-3-trifluoromethylphenyl)-2-methylbutyl] ester, or a pharmaceutically acceptable acid addition salt thereof

i. (R)-phosphoric acid mono[2-amino-4-(4-heptyloxy-3-trifluoromethylphenyl)-2-methylbutyl] ester, or a pharmaceutically acceptable acid addition salt thereof

j. 2-amino-4-(3-cyano-4-heptyloxyphenyl)-2-(phosphoryloxymethyl)butanol, or a pharmaceutically acceptable acid addition salt thereof.

12. 2-Amino-2-[2-(4-heptyloxy-3-trifluoromethylphenyl)ethyl]propane-1,3-diol, or a hydrochloride thereof.

13. A phaiinaceutical composition comprising the compound of claim 1 or 12 and a pharmaceutically acceptable carrier.

Assignments (2)
CHANGE OF NAME Recorded Mar 5, 2026
From: MITSUBISHI TANABE PHARMA CORPORATION
To: TANABE PHARMA CORPORATION
Reel/Frame 073977/0840 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 31, 2008
From: KIUCHI, MASATOSHI; MARUKAWA, KAORU; KOBAYASHI, NOBUTAKA; SUGAHARA, KUNIO
To: MITSUBISHI TANABE PHARMA CORPORATION
Reel/Frame 021324/0965 →
Priority Claims (1)
JP 2005-361363 · Dec 15, 2005 · national
Continuity (1)
Related Publication 20090137530A1 · May 28, 2009