US 4,404,382 AGrant
Piperazinyl-Substituted Imidazoles
Issue Date:1983-09-13
•15 Claims
Abstract
The present invention provides certain piperazinyl-substituted imidazoles which are useful for the treatment of sensitized humans for allergies and anaphylactic reactions.
Metadata
Assignee
- The Upjohn Company
Inventor
- Martin Gall
Application Information
Application Number:US 3624471
Filing Date:1982-03-26
Priority Date:1980-09-17
Art Unit:122
Classifications
IPC:
C07D40100C07D40300A61K 3141
Field of Search:
544360;370
Patent Drawings
This patent does not have any drawings.
Description
Description
1. Background of the Invention
The present invention relates to novel substituted imidazoles. Most particularly, the present invention relates to certain piperazinyl substituted imidazoles. The pharmaceutical use and preparation of these compounds is described in U.S. Pat. No. 4,338,453, which is expressly incorporated herein by reference above.
2. Prior Art
Various imidazoles are known. These compounds have been described as useful for a wide range of uses. Such known imidazole compounds include 1,2,4,5-tetra-substituted imidazoles useful as antitumor, antiviral, antiinflammatory agent agents, and as protective agents against cerebral anoxia or hypoxia such as are described in British Pat. No. 2,016,011 (abstracted in Derwent Farmdoc CPI No. 68606B/38), French Pat. No. 2,132,632 (abstracted in Derwent Farmdoc CPI No. 10105U-B), U.S. Pat. No. 3,651,080, and Belgian Pat. No. 810,117 (abstracted in Farmdoc CPI No. 41717V/23); 1-substituted imidazoles for use in treating inflammation, hypertension, thrombosis and asthma such as described in Japanese Patent Application 109974 (abstracted in Derwent Farmdoc CPI No. 72897B/40); 1,2-di-substituted-4-haloimidazoles-5-acetic acid derivatives for use as diuretics and hypotensives, as described in U.S. Pat. No. 4,207,324; and 1,4,5-trisubstituted imidazoles useful as antiallergic and hypotensive agents such as described in British Pat. No. 1,134,580. U.S. Pat. No. 3,505,350 discloses certain mercapto imidazole derivatives which are useful as antiinflammatory agents.
Summary of the Invention
The present invention particularly provides a compound according to Formula I ##STR1## or a pharmacologically acceptable salt thereof, wherein X.sub.1 is
(a) .dbd.CH--; or
(b) .dbd.C(CH.sub.3)--;
wherein m is zero, one, 2 or 3;
wherein n is zero, one or 2,
wherein R.sub.4 is:
(a) hydrogen;
(b) alkyl of one to three carbon atoms, inclusive;
(c) R.sub.54 OCH.sub.2 --, wherein R.sub.54 is defined below;
(d) --CH(R.sub.35)(OH); or
(e) --R.sub.35 ;
wherein R.sub.5, R.sub.15, R.sub.25 and R.sub.35 are the same or different and are
(i) 2,3, or 4 pyridinyl, or
(ii) phenyl substituted by zero to 2 chloro, fluoro, bromo, alkyl of from one to 3 carbon atoms, or alkoxy of from one to 3 carbon atoms, or
(iii) phenyl substituted by one trifluoromethyl and zero to one of the previous phenyl substituents,
wherein R.sub.6 is:
(a) hydrogen;
(b) --OR.sub.54 ;
(c) alkanoyloxy of from one to 3 carbon atoms; or
(d) alkyl of from one to 3 carbon atoms; with the proviso that when m is zero, R.sub.6 does not contain oxygen;
wherein R.sub.7 is
(i) hydrogen,
(ii) methyl,
(iii) phenylmethyl, or
(iv) phenylethyl,
wherein R.sub.8 is
(i) --R.sub.15 ;
(ii) --CH.sub.2 R.sub.15, or
(iii) --CHR.sub.15 R.sub.25 ;
wherein R.sub.17 is methyl, phenyl, benzyl, or 2-phenylethyl; and wherein R.sub.54 is hydrogen or alkyl of one to 3 carbon atoms; or an enantiomer (when R.sub.4 is --CH(R.sub.35)OH or when R.sub.6 is not hydrogen) or diastereomer (when R.sub.4 is --CH(R.sub.35)OH and R.sub.6 is not hydrogen) of such compound.
Description of the Preferred Embodiments
The present invention particularly provides:
1-[2-(5-Methyl-1-phenyl-1H-imidazol-2-yl)ethyl]-4-phenylpiperazine;
1-(4-Chlorophenyl)-4-[2-(5-methyl-1-phenyl-1H-imidazol-2-yl)ethyl]piperazin e;
1-(4-Fluorophenyl)-4-[2-[1-(4-fluorophenyl)-5-methyl-1H-imidazol-2-yl]ethyl ]piperazine;
1-(4-Chlorophenyl)-4-[2-[1-(4-fluorophenyl)-5-methyl-1H-imidazol-2-yl]ethyl ]piperazine; and
1-[2-[1-(4-Fluorophenyl)-5-methyl-1H-imidazol-2-kyl]ethyl]-4-phenylpiperazi ne.
Claims
I claim:
1. A compound according to formula I ##STR2## or a pharmacologically acceptable salt thereof, wherein X.sub.1 is (a) .dbd.CH--; or (b) .dbd.C(CH.sub.3)--; wherein m is zero, one, 2 or 3; wherein n is zero, one or 2, wherein R.sub.4 is: (a) hydrogen; (b) alkyl of one to three carbon atoms, inclusive; (c) R.sub.54 OCH.sub.2 --, wherein R.sub.54 is defined below; (d) --CH(R.sub.35)(OH); or (e) --R.sub.35 ; wherein R.sub.5, R.sub.15, R.sub.25 and R.sub.35 are the same or different and are (i) 2,3, or 4 pyridinyl, or (ii) phenyl substituted by zero to 2 chloro, fluoro, bromo, alkyl of from one to 3 carbon atoms, or alkoxy of from one to 3 carbon atoms, or (iii) phenyl substituted by one trifluoromethyl and zero to one of the previous phenyl substituents, wherein R.sub.6 is: (a) hydrogen; (b) --OR.sub.54 ; (c) alkanoyloxy of from one to 3 carbon atoms; or (d) alkyl of from one to 3 carbon atoms; with the proviso that when m is zero, R.sub.6 does not contain oxygen; wherein R.sub.7 is (i) hydrogen, (ii) methyl, (iii) phenylmethyl, or (iv) phenylethyl, wherein R.sub.8 is (i) --R.sub.15 ; (ii) --CH.sub.2 R.sub.15, or (iii) --CHR.sub.15 R.sub.25 ; wherein R.sub.17 is methyl, phenyl, benzyl, or 2-phenylethyl; and wherein R.sub.54 is hydrogen or alkyl of one to 3 carbon atoms; or an enantiomer (when R.sub.4 is --CH(R.sub.35)OH or when R.sub.6 is not hydrogen) or diastereomer (when R.sub.4 is --CH(R.sub.35)OH and R.sub.6 is not hydrogen) of such compound.
2. A compound of claim 1, wherein n is zero and R.sub.6 and R.sub.7 are hydrogen.
3. A compound of claim 2, wherein m is 2.
4. A compound of claim 2, wherein m is one or 2, and R.sub.4 is hydrogen, methyl, hydroxymethyl, or --CH(R.sub.35)(OH), wherein R.sub.5 and R.sub.35 are phenyl substituted by zero to 2 chloro, fluoro or bromo.
5. 1-[2-(5-Methyl-1-phenyl-1H-imidazole-2-yl)-ethyl]-4-phenylpiperazine, a compound of claim 4.
6. 1-(4-Chlorophenyl) -4-[2-(5-methyl-1-phenyl-1H-imidazole-2-yl)-ethyl]piperazine, a compound of claim 4.
7. A compound of claim 4, wherein R.sub.4 is methyl.
8. 1-(4-Fluorophenyl)-4-[2-[1-(4-fluorophenyl)-5-met hyl-1H-imidazole-2-yl]ethyl]piperazine, a compound of claim 7.
9. 1-(4-Chlorophenyl)-4-[2-[1-(4-fluorophenyl)-5-methyl-1H-imi dazol-2-yl]ethyl]piperazine, a compound of claim 7.
10. 1-[2-[1-(4-Fluorophenyl)-5-methyl-1H-imidazol-2 -yl]ethyl]-4-phenylpiperazine, a compound of claim 7.
11. A compound of claim 4, wherein R.sub.6 is hydrogen.
12. A compound of claim 1, wherein X.sub.1 is .dbd.CH--.
13. A compound of claim 1, wherein X.sub.1 is .dbd.C(CH.sub.3)--.
14. A compound of claim 1, wherein R.sub.4 is hydrogen.
15. A compound of claim 1, wherein R.sub.4 is methyl or thiomethyl.
Patent Citations (4)
| Patent | Date | Inventor | Cited By |
|---|---|---|---|
| US3362956 | 1968-01-01 | Archer | |
| US3423413 | 1969-01-01 | Priewe et al. | |
| US3491098 | 1970-01-01 | Archer | |
| US3927011 | 1975-12-01 | Nakanishi et al. |