Anti-inflammatory imidazole compounds

OBJECTS OF THE INVENTION
It is an object of the invention to provide the novel compounds of formula I and their non-toxic, pharmaceutically acceptable acid addition salts and their preparation.
It is another object of the invention to provide novel anti-inflammatory compositions and a novel method of treating inflammation in warm-blooded animals.
These and other objects and advantages of the invention will become obvious from the following detailed description.
THE INVENTION
The novel compounds of the invention are selected from the group consisting of a compound of the formula ##STR3## wherein R.sub.1 is selected from the group consisting of ##STR4## R is selected from the group consisting of hydrogen and alkyl of 1 to 5 carbon atoms, R' is selected from the group consisting of hydrogen, alkyl and hydroxyalkyl of 1 to 5 carbon atoms, and aryl of 6 to 10 carbon atoms optionally substituted with at least one member of the group consisting of halogen, --OH, --COOH, CF.sub.3 and alkyl and alkoxy of 1 to 5 carbon atoms, (a) A is alkyl of 1 to 5 carbon atoms, B and G together with the carbon atom to which they are attached are carbonyl or thiocarbonyl and D is selected from the group consisting of alkyl of 1 to 5 carbon atoms and phenyl optionally substituted with at least one member of the group consisting of halogen, --OH, --COOH, --CF.sub.3 and alkyl and alkoxy of 1 to 5 carbon atoms or (b) A and B together form a bond, G is selected from the group consisting of alkyl, alkoxy and alkylthio of 1 to 5 carbon atoms and alkylsulfinyl and alkylsulfonyl of 1 to 5 carbon atoms and D is selected from the group consisting of alkyl of 1 to 5 carbon atoms and phenyl optionally substituted with at least one member of the group consisting of halogen, --OH, --COOH, --CF.sub.3 and alkyl and alkoxy of 1 to 5 carbon atoms or (c) A and B together form a bond, G and D together form a member of the group consisting of ##STR5## wherein X is alkoxy or alkylthio of 1 to 5 carbon atoms, Y and Y' are individually hydrogen or alkyl of 1 to 5 carbon atoms and E is hydrogen or halogen with the proviso when A and B are a bond and G and D together are ##STR6## and R.sub.1 is ##STR7## E is other than hydrogen and its non-toxic, pharmaceutically acceptable acid addition salts.
When A and B together form a bond and G and D together form ##STR8## the compounds of formula I may have the formula ##STR9## respectively.
Examples of alkyl and alkoxy of 1 to 5 carbon atoms are methyl, ethyl, isopropyl, n-propyl and linear and branched butyl and pentyl, methoxy, ethoxy, isopropoxy, n-propoxy and linear and branched butoxy and pentyloxy. Examples of hydroxyalkyl of 1 to 5 carbon atoms are hydroxymethyl, hydroxyethyl, hydroxy-n-propyl, hydroxyisopropyl and linear or branched hydroxybutyl and hydroxypentyl.
Examples of aryl 6 to 10 carbon atoms are phenyl and naphthyl optionally substituted as discussed above. Examples of alkylthio of 1 to 5 alkyl carbon atoms are methylthio, ethylthio, n-propylthio, isopropylthio and linear and branched butylthio and pentylthio. Examples of alkylsulfinyl and alkylsulfonyl of 1 to 5 alkyl carbon atoms are methylsulfinyl, ethylsulfinyl, n-propylsulfinyl, isopropylsulfinyl, linear and branched butylsulfinyl and pentylsulfinyl, methylsulfonyl, ethylsulfonyl, isopropylsulfonyl, n-propylsulfonyl and linear and branched butylsulfonyl and pentylsulfonyl.
Examples of suitable acids for the formation of the non-toxic, pharmaceutically acceptable acid addition salts are inorganic acids such as hydrochloric acid, hydrobromic acid hydriodic acid, nitric acid, sulfuric acid and phosphoric acid and organic acids such as propionic acid, formic acid, benzoic acid, maleic acid, fumaric acid, succinic acid, tartaric acid, citric acid, oxalic acid, glyoxylyic acid, aspartic acid, alkanesulfonic acids such as methanesulfonic acid, and arylsulfonic acid such as benzenesulfonic acids.
Examples of preferred compounds of formula I are those wherein R.sub.1 is ##STR10## and E is halogen, those wherein R.sup.1 is --C.tbd.C--R' and E is halogen, those wherein A and B together are a bond, G and D together are ##STR11## E is halogen, X.sub.a is methoxy or methylthio and Y.sub.a and Y.sub.a ' are individually hydrogen, methyl or ethyl and E is halogen and those wherein A and B together are a bond, G is alkylthio of 1 to 5 carbon atoms and D is optionally substituted phenyl and their non-toxic, pharmaceutically acceptable acid addition salts.
Among the preferred compounds of formula I are
1-(3-bromo-6-ethyl-5-methyl-7-methylthioimidazo[1,2-a]-pyrimidin-2-yl)-2-methyl-2-propen-1-one;
1-[5-bromo-1-(4-ethylphenyl)-2-methylthioimidazol-4-yl]-2-methyl-2-propen-1-one;
1-[5-bromo-1-(4-methoxyphenyl)-2-methylthioimidazol-4-yl]-2-propen-1-one;
1-(3-bromo-6-ethyl-7-methoxy-5-methylimidazo[1,2-a]-pyrimidin-2-yl)-2-propen-1-one;
1-(3-bromo-6-ethyl-7-methoxy-5-methylimidazol[1,2-a]-pyrimidin-2-yl)-3-phenyl-2-propyn-1-one and their non-toxic, pharmaceutically acceptable acid addition salts.
The novel process of the invention for the preparation of compounds of formula I wherein E is hydrogen comprises oxidizing a compound of the formula ##STR12## wherein B,G,D,A and R.sub.1 are defined as above with an oxidizing agent such as manganese dioxide and optionally salifying the corresponding compound of formula I. The oxidation is preferably effected in an organic solvent such as chloroform at reflux.
The compounds of formula IV may be prepared by reacting a compound of the formula ##STR13## wherein A,B,G and D have the above definitions with a source of R.sub.1.sup.- carbonions such as Grignard reagent of the formula R.sub.1 MgBr III or an alkyllithium of the formula R.sub.1 -Li III.sub.A wherein R.sub.1 has the above definition preferably in an inert organic solvent such as tetrahydrofuran.
A process for the preparation of compounds of formula I.sub.B wherein E is halogen ##STR14## wherein Hal represents a halogen atom, R.sub.1 ' is ##STR15## wherein R and R' have the above definitions and (a) A' is alkyl of 1 to 5 carbon atoms, B' and G' together with the carbon atom to which they are attached are carbonyl or thiocarbonyl and D' is alkyl of 1 to 5 carbon atoms or phenyl optionally substituted with at least one member of the group consisting of halogen, --OH, --COOH, --CF.sub.3 and alkyl and alkoxy of 1 to 5 carbon atoms or (b) A' and B' together form a bond, G' is alkyl or alkylthio of 1 to 5 carbon atoms and D' is alkyl of 1 to 5 carbon atoms or phenyl optionally substituted with at least one member of the group consisting of halogen, --OH, --COOH, CF.sub.3 and alkyl and alkoxy of 1 to 5 carbon atoms or (c) A' and B' are a bond, G' and D' together are ##STR16## wherein X, Y and Y' are as defined above comprises reacting a compound of the formula ##STR17## wherein A', B', G', D' and R'.sub.1 are defined as above with a N-halosuccinimide optionally followed by salification of the compound of formula I.sub.B. The reaction is preferably effected in an organic solvent such as chloroform or carbon tetrachloride.
A process for the preparation of a compound of the formula ##STR18## wherein R.sub.1, D and E are defined as above, Alk is alkyl of 1 to 5 carbon atoms and n is 1 or 2 comprises oxidizing a compound of the formula ##STR19## wherein D,E,R.sub.1 and Alk have the above definition and n' is 0 or 1 with an oxidizing agent such as sodium metaperiodate to obtain the compound of formula I.sub.D which may be optionally salified. The reaction is preferably effected in a suitable organic solvent such as aqueous alkanol such as methanol and at a suitable temperature such as about 50.degree. C.
To prepare the alkylsulfinyl derivatives, the compounds of formula I.sub.C wherein n' is 0 are reacted with one equivalent of oxidizing agent. The alkylsulfonyl compounds of formula I.sub.D wherein n is 2 may be prepared by oxidizing the compound of formula I.sub.C wherein n' is 0 with at least two equivalents of oxidizing agent or oxidize the compound of formula I.sub.C wherein n' is 1 with at least one equivalent of oxidizing agent.
A process for the preparation of the compounds of formula I wherein at least one of R.sub.1 and D contains a hydroxy group comprises removing a protective group from a compound of the formula ##STR20## wherein A, B, G and E have the above definitions, D" is D or a precursor of a group D with a protected hydroxy and R".sub.1 is R.sub.1 or a precursor of a group R.sub.1 with a protected hydroxy, with the proviso that at least one of D" and R".sub.1 is a precursor of a group containing a protected hydroxy. The compounds of formula V may be prepared by one of the previous processes using starting materials wherein R.sub.1 and/or D contains protected hydroxy groups.
As will be appreciated from the above, certain of the compounds of the invention possess free hydroxy groups, and it may thus be necessary or desirable to protect any free hydroxy groups during the preparation of the said compounds. In such situations, the protecting group will remain in place throughout the duration of the process sequence, and will itself be removed by traditional methods (e.g. by hydrolysis) as the final step thereof.
For example, if R' is hydroxyalkyl of 1 to 5 carbon atoms, the protecting group used will conveniently be of the type customarily employed for the protection of aliphatic hydroxy groups such as tetrahydropyranyl, although other suitable protecting groups will be apparent to those skilled in the art. Thus, a compound of formula III or III.sub.A wherein R' of R.sub.1 is a suitably protected hydroxyalkyl of 1 to 5 carbon atoms will be taken and reacted with the appropriate compound of formula II. The protected derivative of formula IV thereby obtained may then be elaborated as appropriate according to one or more of processes (A) to (C) above, the protecting group on the hydroxy substituent being retained for the remaining steps of the synthetic sequence, its removal consituting the final step thereof. Such a process is described in Examples 22 and 23.
Similarly, in those cases wherein R' is hydroxy-substituted aryl of 6 to 10 carbon atoms and/or D is a hydroxy-substituted phenyl, the protecting group used will conveniently be of the type customarily employed for the protection of aromatic hydroxys, a typical example being benzyl although as before other suitable protecting groups will be apparent to those skilled in the art. Again, the protected derivative of formula IV involved as an intermediate in the synthetic sequence may be elaborated as appropriate according to one or more of processes (A) to (C) above. As before, the protecting group on the hydroxy will be retained for the remaining steps of the synthetic sequence and its removal will constitute the final step thereof and such a process is described in Example 14.
The compounds are basic in character and their acid addition salts may be obtained by reacting approximately stoichiometric amounts of the compound of formula I and the appropriate acid in a suitable solvent with or without isolation of the compound of formula I
The novel anti-inflammatory compositions of the invention are comprised of an anti-inflammatory effective amount of at least one compound of formula I and their non-toxic, pharmaceutically acceptable acid addition salts and an inert pharmaceutical carrier or excipient. The compositions may be in the form of tablets, dragees, capsules, powders, suppositories, aerosols and injectable solutions or suspensions.
Examples of suitable excipients are talc, gum arabic, lactose, starch, magnesium stearate, cocoa butter, aqueous or nonaqueous vehicles, animal or vegetable fats, paraffin derivatives, glycols, various wetting, dispersing or emulsfying agents and/or preservatives.
The compositions of the invention possess very interesting pharmacological properties; particularly they have been found to possess an anti-inflammatory effect, notably in their ability to moderate inflammatory/immune cell function by restricting arachiodonic acid release and consequential eicosanoid biosynthesis. They are useful for the treatment of inflammatory and immunological disorders such as rheumatoid arthritis, osteoarthritis and psoriasis. The preferred active ingredients are as indicated above.
The novel method of the invention for treating inflammation in warm-blooded animals, including humans, comprises administering to warm-blooded animals an anti-inflammatorily effective amount of at least one compound of formula I and their non-toxic, pharmaceutically acceptable acid addition salts. The compounds may be administered orally, rectally or parenterally and the usual daily dose in 0.001 to 2.5 mg/kd depending on the conditions treated, the specific compound and method of administration.
Imidazole-4-carboxaldehydes of formula II may be prepared by a modification of the procedures described in Helv. Chim. Acta. 1960, Vol. 43, p. 1787 and Tetrahedron, 1963, Vol. 19, p. 1883. An example of such a preparation is given below as Preparation A.
Imadazo[1,2-a]pyrimidine-2-carboxaldehydes of formula II may be prepared as in British patent application No. 2,128,989 or by methods analogous thereto, as also may compounds of formula I.sub.A wherein A' and B' together are a bond, G' and D' together are ##STR21## wherein X, Y, and Y' are as defined above and ##STR22## in which R is as defined above which, while not themselves being compounds of the invention, are nevertheless useful intermediates for the compounds of formula I.sub.B. An example of such a preparation is described in Preparation H below.
Imidazol[1,2-a]pyridine-2-carboxaldehydes of formula II may conveniently be prepared using a variant of the process described in British patent application No. 2,128,989 from the corresponding imidazo[1,2-a]pyridine-2-carboxylate esters which, in turn, may themselves be obtained by the method detailed in J. Org. Chem., 1965, Vol. 30, p. 2403.

In the following examples there are described several preferred embodiments to illustrate the invention. However, it is to be understood that the invention is not intended to be limited to the specific embodiments.
Preparation A
1-(4-methoxyphenyl)-2-methylthioimidazole-4-carboxaldehyde ##STR23##
Step (a):
A mixture of 18 g of glucose, 12.3 of p-methoxyaniline, 36 ml of water and 1 ml of acetic acid was heated on a steam-bath for 15 minutes after which time a clear solution was formed. 7.6 g of ammonium isothiocyanate and 6 g of acetic acid were added and the solution was heated on a steam-bath for 2 hours after which time solidification occurred. The solid was digested with hot water, filtered, stirred in methanol for 1 hour, filtered, washed with ether and dried to obtain 10.5 g (32%) of intermediate (1) melting at 215.degree.-6.degree. C. (Tetrahedron, 1963, Vol. 19, page 1883, m.p. 215.degree.-6.degree. C.)
Step (b):
A mixture of 10.5 g of intermediate (1) 5.0 g of iodomethane and 5.0 g of potassium carbonate was stirred in 50 ml of dimethylformamide for 1 hour and then was diluted with water to crystallize 7.6 g (69%) of intermediate (2) as a brown solid which was used directly in the next step.
Step (c):
A mixture of 7.6 g of intermediate (2) and 16.0 g of sodium metaperiodate was stirred in 100 ml of aqueous methanol of 10% for 1 hour. The solution was concentrated under reduced pressure and diluted with water to crystallize 2.7 g of aldehyde (3) (49% yield) as colorless crystals after crystallization from ethanol melting at 118.degree.-20.degree. C.
Compounds B to E were prepared analogously. Compound F was prepared as described in published British patent application No. 2,128,989, and compound G was prepared by an analogous method. Compounds J and K were prepared as indicated in Example 1 Step A. The Yield, melting point and analytical data of starting compounds of formula II are given in Tables A and B. Yield, melting point and analytical data of intermediates of formula I.sub.A are given in Table C.
EXAMPLE 1
1-(3-bromo-6-ethyl-5-methyl-7-methylthio-imidazo[1,2-a]pyrimidin-2-yl)-2-methyl-2-propen-1-one
STEP A
1-(6-ethyl-5-methyl-7-methylthioimidazo[1,2-a]pyrimidin-2-yl)-2-methyl-2-propen-1-one
(Method A)
1.2 g (4.78 mmol) of 6-ethyl-5-methyl-7-methylthioimidazo[1,2-a]pyrimidine-2-carboxaldehyde were added to a solution of 7.17 mmol of 2-propenyl magnesium bromide in 50 ml of dry tetrahydrofuran under nitrogen and the mixture was stirred at room temperature for 3 hours. The reaction mixture was quenched with aqueous ammonium chloride and was extracted with chloroform (3.times.50 ml). The organic layer was dried over MgSO.sub.4 and the solvent was removed under reduced pressure. The residual oil was purified by flash chromatography over 25 mg of silica, (dichloromethane:ethyl acetate 1:0 gradually changing to 0.1) to obtain 1.17 g (84%) of the 2-methyl-2-propen-1-ol as colorless crystals melting at 116.degree.-8.degree. C. .nu..sub.Max (KBr) 3160, 2960, 2920, 2870 and 1610 cm.sup.-1.
A solution of 1.4 g (4.78 mmol) of 2-methyl-2-propen-1-ol in 200 ml of chloroform was heated under reflux with 5 g of manganese dioxide for 2 hours and then was filtered hot through celite. The solvent was removed under reduced pressure to obtain 1.25 g (90%) of 1-(6-ethyl-5-methyl-7-methylthioimidazol[1,2-a]pyrimidin-2-yl)-2-methyl-2-propen-1-one as yellow crystals melting at 136.degree.-7.degree. C. (from ethyl acetate).
STEP B
1-(3-bromo-6-ethyl-5-methyl-7-methylthioimidazo[1,2-a]pyrimidin-2-yl)-2-methyl-2-propen-1-one
Method B
A solution of 1.0 g (3.63 mmol) of 1-(6-ethyl-5-methyl-7-methylthioimidazo[1,2-a]pyrimidin-2-yl)-2-methyl-2-propen-1-one in 50 ml of chloroform was treated with 0.71 g (4.0 mmol) of N-bromosuccinimide. After 20 minutes at room temperature, the solvent was removed under reduced pressure and the residue was purified by flash chromatography (silica, 25 g: dichloromethane) to obtain 1.1 g (87%) of 1-(3-bromo-6-ethyl-5-methyl-7-methylthioimidazo[1,2-a]pyrimidin-2-yl)-2-methyl-2-propen-1-one in the form of pale yellow crystals melting at 87.degree.-9.degree. C.
EXAMPLES 2 TO 13
Using the procedure of Step A and/or Step B of Example 1, the compounds of Examples 2 to 13 were prepared.
EXAMPLE 2
(3-bromo 6-ethyl 7-methoxy 5-methylimidazo[1,2-a]pyrimidin-2-yl)isopropenyl methanone
EXAMPLE 3
(3-chloro 6-ethyl 7methoxy 5-methylimidazo[1,2-a]pyrimidin-2-yl)isopropenyl methanone
EXAMPLE 4
(7-methoxy 5-methylimidazo[1,2-a]pyrimidin-2-yl)ethenyl methanone
EXAMPLE 5
(3-bromo 6-ethyl 7-methoxy 5-methylimidazo[1,2-a]pyrimidin-2-yl)ethenyl methanone
EXAMPLE 6
[1-(4-ethylphenyl) 2-imidazol-4-yl]isopropenyl methanone
EXAMPLE 7
[1-(4-ethylphenyl) 5-bromo 2-thiomethylimidazol-4-yl]isopropenyl methanone
EXAMPLE 8
[1-(4-methoxyphenyl) 5-bromo 2-thiomethylimidazol-4-yl]isopropenyl methanone
EXAMPLE 9
[1-(4-methoxyphenyl) 5-chloro 2-thiomethylimidazol-4-yl]isopropenyl methanone
EXAMPLE 10
[1-(4-methylphenyl) 5-bromo 2-thiomethylimidazol-4-yl]isoproprnyl methanone
EXAMPLE 11
[ 1-(4-methylphenyl) 5-bromo 2-thioisopropylimidazol-4-yl]isopropenyl methanone
EXAMPLE 12
[1-(4-fluorophenyl) 5-bromo 2-thiomethylimidazol-4-yl]isopropenyl methanone
EXAMPLE 13
[1-(4-methoxyphenyl) 5-bromo 2-thiomethylimidazol-4-yl]ethenyl methanone
EXAMPLE 14
[5-bromo-1-(4-hydroxyphenyl)-2-methylthioimidazol-4-yl]-2-methyl-2-propen-1-one
STEP A
1-(4-benzyloxyphenyl)-2-methylthioimidazole-4-carboxaldehyde
p-benzyloxyaniline was reacted according to method of preparation A to obtain 1-(4-benzyloxyphenyl)-2-methylthioimidazole-4-carboxaldehyde
STEP B
[1-(4-benzyloxyphenyl)-2-methylthioimidazol-4-yl]2-methyl-2-propen-1-one
The compound of Step A was reacted by the method of Step A of Example 1 to obtain [1-(4-benzyloxyphenyl)-2-methylthioimidazol-4-yl]-2-methyl-2-propen-1-one
STEP C
[1-(4-benzyloxyphenyl)-5-bromo-2-methylthioimidazol-4-yl]-2-methyl-2-propen-1-one
The product of Step B was reacted by the method of Step B of Example 1 to obtain [1-(4-benzyloxyphenyl)-5-bromo-2-methylthioimidazol-4-yl]-2-methyll-2-propen-1-one.
STEP D
[5-bromo-1-(4-hydroxyphenyl)-2-methylthioimidazol-4-yl]2-methyl-2-propen-1-one
2.7 g (6.1 mmol) of [1-(4-benzyloxyphenyl)-5-bromo-2-methylthioimidazol-4-yl]-2-methyl-2-propen-1-one were heated for 24 hours at 30.degree. C. in 25 ml of trifluoroacetatic acid. Removal of trifluoroacetic acid was effected at 30.degree. C. under reduced pressure followed by addition of iced water to obtain an oil which was extracted with ether and purified by flash chromatography on silica (5% ethyl acetate in petroleum ether) to obtain 1.9 g (88%) of [5-bromo-1-(4-hydroxyphenyl)-2-methylthioimidazol-4-yl]2-methyl-2-propen-1-one in the form of pale yellow crystals melting at 159.degree.-161.degree. C.
EXAMPLE 15
(1-ethyl 5-bromo 2-thioisopropyl imidazol-4-yl)isopropenyl methanone
Using the method of Example 1, the corresponding compound of formula I.sub.A was reacted to obtain the compound of Example 15.
EXAMPLE 16
[5-chloro-1-(4-ethylphenyl)-2-(prop-2-ylsulfinyl)-imidazol-4-yl]-2-methyl-2-propen-1-one
A mixture of 3.0 g (8.6 mmol) of [5-chloro-1-(4-ethylphenyl)-2-(prop-2-ylthio)-imidazol-4-yl]-2-methyl-2-propen-1-one and 2.3 g (11 mmol) of sodium metaperiodate was heated at 50.degree. C. for 3 hours in 30 ml of 90% aqueous methanol. The mixture was cooled and poured into water. Extraction with dichloromethane yielded an oil which was purified by flash chromatography on silica (20% ethyl acetate in petroleum ether) to obtain 1.3 g (41%) of [5-chloro-1-(4-ethylphenyl)-2-(prop-2-ylsulfinyl)-imidazol-4-yl]-2-methyl-2-propen-1-one as cream-colored crystals melting at 83.degree.-4.degree. C.
EXAMPLE 17
[1-(4-ethylphenyl)5-chloro 2-ethylsulfininylimidazol-4-yl]isopropenyl methanone
Using the method of Example 16, the corresponding compound of formula I.sub.C was reacted to obtain the compound of Example 17.
EXAMPLES 18 TO 21
Using the methods of Step A or B of Example 1, the corresponding compounds of formulae II or I.sub.A respectively were reacted to obtain the compounds of Examples 18 to 21.
EXAMPLE 18
(6-ethyl 7-methoxy 5-methylimidazo [1,2-a]pyrimidin-2-yl)phenylethynyl methanone
EXAMPLE 19
1-(6-ethyl 7-methoxy 5-methylimidazo[1,2-a]pyrimidin-2-yl) (3,3-dimethylbut-1-ynyl)methanone
EXAMPLE 20
(3-bromo 6-ethyl 7-methoxy 5-methylimidazo[1,2-a]pyrimidin-2-yl) (3,3-dimethylbut-1-ynyl)methanone
EXAMPLE 21
(3-bromo 6-ethyl 7-methoxy 5-methylimidazo[1,2-a]pyrimidin-2-yl) (2-phenylethy-1-yl)methanone
EXAMPLE 22
1-(3-bromo-6-ethyl-7-methoxy-5-methyl-imidazo[1,2-a]pyrimidin-2-yl)-4-hydroxy-2-butyn-1-one
STEP A
1-(6-ethyl-7-methoxy-5-methylimidazo[1,2-a]pyrimidin-2-yl)-4-(tetrahydropyran-2-yloxy)-2-butyn-1-one
6-ethyl-7-methoxy-5-methylimidazo[1,2-a]pyrimidin-2-carboxaldehyde and 3-(tetrahydropyran-2-yloxy)-1-propynyl-magnesium bromide [J. Chem. Soc., 1950, 3646] were reacted by the method of Step A of Example 1 to obtain 1-(6-ethyl-7-methoxy-5-methylimidazol[1,2-a]pyrimidin-2-yl)-4-(tetrahydropyran-2-yloxy)-2-butyn-1-one.
STEP B
1-(3-bromo-6-ethyl-7-methoxy-5-methylimidazo[1,2-a]pyrimidin-2-yl)-4-(tetrahydropyran-2-yloxy)-2-butyn-1-one
The compound of Step A was reacted by the procedure of Step B of Example 1 to obtain 1-3-(bromo-6-ethyl-7-methoxy-5-methylimidazo[1,2-a]pyrimidin-2-yl)-4-(tetrahydropyran-2-yloxy)-2-butyn-1-one.
STEP C
1-(3-bromo-6-ethyl-7-methoxy-5-methylimidazo[1,2-a]pyrimidin-2-yl)-4-hydroxy-2-butyn-1-one
A solution of 5.0 g (11.5 mmol) of 1-(3-bromo-6-ethyl-7-methoxy-5-methylimidazo[1,2-a]pyrimidin-2-yl)-4-(tetrahydropyran-2-yloxy)-2-butyn-1-one in a mixture of 100 ml of methanol and 35 ml of 2N hydrochloric acid stood at room temperature for 30 minutes and then was neutralized with aqueous sodium bicarbonate. Extraction with chloroform gave an oil which was chromatographed over silica (chloroform:ether:methanol 100:0:0 gradually changing to 0:95:5) to obtain 1.3 g (32%) of 1-(3-bromo-6-ethyl-7-methoxy-5-methylimidazo[1,2-a]pyrimidin-2-yl)-4-hydroxy-2-butyn-1-one as off-white crystals melting at 212.degree.-3.degree. C. (decomp.).
EXAMPLE 23
1-(6-ethyl-7-methoxy-5-methylimidazo[1,2-a]pyrimidin-2-yl)-4-hydroxy-2-butyn-1-one
STEP A
1-(6-ethyl-7-methoxy-5-methylimidazo[1,2-a]pyrimidin-2-yl)-4-(tetrahydropyran-2-yloxy)-2-butyn-1-one
Using the procedure of Step A of Example 22, 1-(6-ethyl-7-methoxy-5-methylimidazo[1,2-a]pyrimidin-2-yl)-4-(tetrahydropyran-2-yloxy)-2-butyn-1-one was prepared.
STEP B
1-(6-ethyl-7-methoxy-5-methylimidazo[1,2-a]pyrimidin-2-yl)-4-hydroxy-2-butyn-1-one
Using the method of Step C of Example 22, the compound of Step A was reacted to obtain a 1-(6-ethyl-7-methoxy-5-methylimidazol[1,2-a]pyrimidin-2-yl)-4-hydroxy-2-butyn-1-one.
EXAMPLES 24 TO 28
Using the methods of Step A or B of Example 1, the corresponding compounds of formula II or I.sub.A respectively were reacted to obtain the compounds of Examples 24 to 28. The yield, melting point and analytical data of compounds of formula I are given in Tables 1 to 4.
EXAMPLE 24
(3-bromo 6-ethyl 7-methoxy 5-methylimidazo[1,2-a]pyrimidin-2-yl) (propyn-1-ynyl)methanone
EXAMPLE 25
(3-bromoimidazo[1,2-a]pyridin-2-yl)isopropenyl methanone (chlorohydrate)
EXAMPLE 26
(imidazo[1,2-a]pyridin-2-yl)isopropenyl methanone
EXAMPLE 27
(imidazo [1,2-a]pyridin-2-yl) (2-phenylethyn-1-yl)methanone
EXAMPLE 28
3-bromoimidazo[1,2-a]pyridin-2-yl (2-phenylethyn-1-yl)methanone
TABLE A__________________________________________________________________________ ##STR24## Yield IR (KBr disc) M.p. Theory/Found (%)PREP G D (%) (cm.sup.-1) (.degree.C.) Formula M.W. C H N__________________________________________________________________________A MeS ##STR25## 49 3130,1690,1670 118-20 C.sub.12 H.sub.12 N.sub.2 O.sub.2 248.3 58.05 57.65 4.87 4.88 11.28 11.09B MeS ##STR26## 80 3130,1668,1650 88-90 C.sub.13 H.sub.14 N.sub.2 OS 246.3 63.39 63.44 5.73 5.73 11.37 11.41C MeS ##STR27## 83 1680 111-3 C.sub.12 H.sub.12 N.sub.2 OS 232.3D iPrS ##STR28## 75 1670 63-4 C.sub.14 H.sub.16 N.sub.2 OS 260.3E MeS ##STR29## 90 1690,1675 130-1 C.sub.11 H.sub.9 FN.sub.2 OS 236.3__________________________________________________________________________
TABLE B__________________________________________________________________________ ##STR30## Theory/Found (%)PREP X Y Y' Yield (%) IR (KBr disc) (cm.sup.-1) M.p. (.degree.C.) Formula M.W. C H N S__________________________________________________________________________F MeO Et Me 72 3120, 3000, 2980, 185-6 C.sub.11 H.sub.13 N.sub.3 O.sub.2 219.2 60.26 5.98 19.17 2950, 1690, 1640 59.97 5.97 19.05G MeS Et Me 85 3098, 2960, 2915, 203-4 C.sub.11 H.sub.13 N.sub.3 OS 235.3 56.15 5.58 17.85 13.63 2860, 1675, 1610 56.35 5.58 17.95 13.34__________________________________________________________________________
TABLE C__________________________________________________________________________ ##STR31## Theory/Found (%)PREP X Y Y' R Yield (%) IR (KBr disc) (cm.sup.-1) M.p. (.degree.C.) Formula M.W. C H N S__________________________________________________________________________H MeS Et Me Me 76 2970, 1630, 1615 136-7 C.sub.14 H.sub.17 N.sub.3 OS 275.4 61.06 6.24 15.25 11.64 60.91 6.22 15.17 11.54J MeO Et Me Me 35 3130, 1640 148-50 C.sub.14 H.sub.17 N.sub.3 O.sub.2 259.3 64.85 6.61 16.20 64.67 6.57 16.12K MeO H Me Me 56 3150, 2980, 2950, 151 C.sub.12 H.sub.13 N.sub.3 O.sub.2 231.25 62.32 5.68 18.16 1625 62.20 5.70 18.14__________________________________________________________________________
TABLE 1__________________________________________________________________________ ##STR32## IR Yield (KBr disc) M.p. Theory/Found (%)Ex X Y Y' E R Method (%) (cm.sup.-1) (.degree.C.) Formula M.W. C H N Hal S__________________________________________________________________________1 MeS Et Me Br Me B 87 2960, 2920, 87-9 C.sub.14 H.sub.16 BrN.sub.3 OS 354.3 47.46 4.56 11.86 22.55(Br) 9.05 1640, 1600 47.32 4.56 11.82 22.54 9.022 MeO Et Me Br Me B 87 2960, 1635, 101-2 C.sub.14 H.sub.16 BrN.sub.3 O.sub.2 338.2 49.71 4.78 12.42 23.63(Br) 1625 49.73 4.72 12.31 23.673 MeO Et Me Cl Me B 62 2965, 1625 111-2 C.sub.14 H.sub.16 ClN.sub.3 O.sub.2 293.8 57.24 5.50 14.30 12.07(Cl) 57.03 5.49 14.25 12.174 MeO H Me Br Me B 98 3070, 2950, 145-6 C.sub.12 H.sub.12 BrN.sub.3 O.sub.2 310.15 1630 decomp5 MeO Et Me Br H B 47 2970, 2940, 120-3 C.sub.13 H.sub.14 BrN.sub.3 O.sub.2 324.2 48.16 4.36 12.96 24.65(Br) 2875, 1670, decomp 48.05 4.32 12.73 24.45 1625__________________________________________________________________________
TABLE 2__________________________________________________________________________ ##STR33##Ex-am- Meth- Yield M.p. Theory/Found (%)ple G D E R od (%) (.degree.C.) Formula M.W. C H N S Other__________________________________________________________________________ IR (KBr disc) (cm.sup.-1) 6 MeS ##STR34## H Me A 43 3120,1636, 1626,1611 46-7 C.sub.16 H.sub.18 N.sub.2 OS 286.4 67.10 67.18 6.33 6.24 9.78 9.77 11.19 11.23 7 MeS ##STR35## Br Me B 77 1636,1620 94-6 C.sub.16 H.sub.17 BrN.sub.2 OS 365.3 52.61 52.62 4.69 4.69 7.67 7.67 IR (cm.sup.-1) 8 MeS ##STR36## Br CH.sub.3 B 84 1630,1620, 1605 128-9 C.sub.15 H.sub.15 BrN.sub.2 O.sub.2 367.3 49.05 48.86 4.12 4.10 7.63 7.55 21.76 (Br) 21.74 9 MeS ##STR37## Cl CH.sub.3 B 93 1630,1620, 1600 110-1 C.sub.15 H.sub.15 ClN.sub.2 O.sub.2 322.8 55.81 55.12 4.68 4.74 8.68 8.53 10.98 (Cl) 11.3910 MeS ##STR38## Br CH.sub.3 B 52 1630,1610 89-90 C.sub.15 H.sub.15 BrN.sub.2 OS 351.3 51.29 51.09 4.30 4.29 7.98 7.89 22.75 (Br) 22.8311 iPrS ##STR39## Br CH.sub.3 B 66 1635,1615, 1605 135-6 C.sub.17 H.sub.19 BrN.sub.2 OS 379.3 53.83 53.76 5.05 5.07 7.39 7.33 8.45 (S) 8.4312 MeS ##STR40## Br CH.sub.3 B 75 1635,1595 99-101 C.sub.14 H.sub.12 BrFN.sub.2 OS 355.2 47.33 47.37 3.41 3.48 7.81 7.81 9.02 (S) 9.0513 MeS ##STR41## Br H B 68 1655,1600 117-9 C.sub.14 H.sub.13 BrN.sub.2 O.sub.2 353.2 47.60 47.36 3.71 3.75 7.93 7.79 22.62 (Br) 22.7214 MeS ##STR42## Br CH.sub.3 B 86 3220,1610, 1590 159-61 C.sub.14 H.sub.13 BrN.sub.2 O.sub.2 353.2 47.60 47.63 3.71 3.72 7.93 7.8215 iPrS Et Br CH.sub.3 B 53 2960,1635, 1590 oil C.sub.12 H.sub.17 BrNO.sub.2 S 317.2 45.43 44.98 5.40 5.37 8.83 8.6916 iPrSO ##STR43## Cl CH.sub.3 C 41 1640,1610, 1595 83-4 C.sub.18 H.sub.21 ClN.sub.2 O.sub.2 364.817 EtSO ##STR44## Cl CH.sub.3 C 33 1640,1610, 1600 76-8 C.sub.17 H.sub.19 ClN.sub.2 O.sub.2 350.8__________________________________________________________________________
TABLE 3__________________________________________________________________________ ##STR45## Meth- Yield M.p. Theory/Found (%)Ex X Y Y' E R' od (%) IR (cm.sup.-1) (.degree.C.) Formula M.W. C H N Hal__________________________________________________________________________18 MeO Et Me H Ph A 86 2197,1630 194-6 C.sub.19 H.sub.17 N.sub.3 O.sub.2 319.4 71.46 5.37 13.16 71.33 5.42 13.1119 MeO Et Me H .sub.-t-Bu A 71 2965,2215, 133-5 C.sub.17 H.sub.21 N.sub.3 O.sub.2 299.3 68.21 7.07 14.04 68.19 7.09 14.06 163520 MeO Et Me Br .sub.-t-Bu B 86 2970,2930, 186-7 C.sub.17 H.sub.20 BrN.sub.3 O.sub.2 378.3 53.97 5.34 11.10 21.12(Br) 2870,2200, 53.72 5.33 10.97 20.89 1640,162021 MeO Et Me Br Ph B 79 3050,2960, 187- C.sub.19 H.sub.16 BrN.sub.3 O.sub.2 398.3 57.30 4.06 10.55 20.06(Br) 2920,2200, 190 57.24 4.09 10.45 20.11 163022 MeO Et Me H CH.sub.2 OH A 41 3400,3125, 176- C.sub.14 H.sub.15 N.sub.3 O.sub.3 273.3 61.53 5.53 15.38 2210,1635 186 (decomp)23 MeO Et Me Br CH.sub.2 OH B 28 3250,2980, 212-3 C.sub.14 H.sub.14 BrN.sub.3 O.sub.3 352.2 47.74 4.01 11.93 22.69(Br) 2880,2220, (decomp) 47.63 4.08 11.78 22.36 163024 MeO Et Me Br CH.sub.3 B 93 2960,2230, 170-2 C.sub.14 H.sub.14 BrN.sub.3 O 320.2 52.51 4.42 13.12 24.96(Br) 2205,1630 (decomp)__________________________________________________________________________
TABLE 4__________________________________________________________________________ ##STR46## Yield M.p. Theory/Found (%)Ex X Y Y' E R.sub.1 Method (%) IR (cm.sup.-1) (.degree.C.) Formula M.W. C H N Hal__________________________________________________________________________25 H H H Br CMeCH.sub.2 B 79 3070, 2540, 140-2 C.sub.11 H.sub.9 BrN.sub.2 O 301.6 43.81 3.35 9.28 1650 (HCl 43.57 3.41 9.11 salt)26 H H H H CMeCH.sub.2 A 77 3145, 3100, 93-4 C.sub.11 H.sub.10 N.sub.2 O 186.2 70.95 5.42 15.04 3080, 3040, 71.08 5.40 15.03 163527 H H H H CCPh A 80 3140, 3100, 168 C.sub.16 H.sub.10 N.sub.2 O 246.3 78.03 4.10 11.37 3080, 3050, 77.96 4.23 11.31 2190, 163028 H H H Br CCPh B 74 3080, 3050, 133-4 C.sub.16 H.sub.9 BrN.sub.2 O 325.15 59.10 2.80 8.61 24.57(Br) 2200, 1630 59.01 2.92 8.60 24.66__________________________________________________________________________
EXAMPLE 29
Tablets containing 20 mg of the compound of Example 1 or 7 and sufficient excipient of lactose, starch, talc and magnesium stearate for a final tablet weight of 100 mg were prepared.
BIOCHEMICAL ACTIVITY
The inhibition of ionophore-stimulated release of free arachidonic acid from [.sup.14 C]-arachidonic acid pre-labelled rat peritoneal neutrophils was studied using modifications of the method of Ahnfelt-Ronne and Arrigoni-Martelli [Biochemical Pharmacol., (1982) Vol. 31, p. 2619]. The results below show the micromolar concentrations of test compound required to inhibit, by 50% compared to controls, the release of radiolabelled products into supernatant liquid (IC.sub.50 -.mu.M).
______________________________________ Example IC.sub.50 - .mu.M______________________________________ 1 6.8 2 17 3 21 4 7.4 5 1.7 6 3.8 7 2.5 8 7.2 9 9.1 10 10 11 3.7 12 15 13 2.3 14 >10 15 17 16 4.4 17 -- 18 12 19 16 20 4.2 21 1.5 22 59 23 46 24 7.2 25 28 26 >100 27 41 28 5.2______________________________________
Various modifications of the compounds and methods of the invention may be made without departing from the spirit or scope thereof and it is to be understood that the invention is intended to be limited only as defined in the appended claims.

Anti-inflammatory imidazole compounds

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