Patent Application
20060004202
The present invention relates to a novel process for the preparation of Imiquimod and novel hydroxylamine and hydrazine derivatives useful as intermediates for its preparation.
Imiquimod, 4-amino-1-isobutyl-1H-imidazo[4,5-c]quinoline (A), is an antiviral and immunomodulating medicament, disclosed in U.S. Pat. No. 4,689,338.
A number of synthetic methods for the preparation of Imiquimod are known, some of which make use of the corresponding 4-chloro-1H-imidazo[4,5-c]quinoline (I) as an intermediate. One of these methods is disclosed in U.S. Pat. No. 4,689,338 which comprises as the last step the following reaction:
The chlorine atom at the 4-position in the intermediate (I) is replaced by an amino group by treatment with ammonia for 18 hours at 155° C. in a steel autoclave. Said reaction is carried out under conditions involving temperatures and pressures which require the use of specific industrial equipment. There is therefore the need for alternative methods for the preparation of Imiquimod, which are more industrially suitable.
It has now surprisingly been found that the intermediate (I), described above, can be conveniently transformed into Imiquimod by reaction with hydrazine, hydroxylamine or a derivative thereof. The novel process for the preparation of Imiquimod does not involve the use of potentially dangerous or problematic reaction conditions. The advantages of this process will be appreciated by the following description.
An object of the invention is a process for the preparation of Imiquimod, 4-amino-1-isobutyl-1H-imidazo[4,5-c]quinoline, comprising the reaction of 4-chloro-1-isobutyl-1H-imidazo[4,5-c]quinoline, of formula (I)
with a compound of formula (II)
NH2—X (II)
wherein X is an —OR or —NR1R2 group in which R is hydrogen, a C1-C6 alkyl, aryl-C1-C4 alkyl, aryl or —SO3H (sulfonic) group; and each of R1 and R2 is independently hydrogen, a C1-C6 alkyl, aryl-C1-C4 alkyl, aryl or —SO2R3 group, wherein R3 is an aryl group; and, if necessary, the reaction with a reducing agent.
A R, R1 or R2 C1-C6 alkyl group, which may be straight or branched, is preferably a C1-C4 alkyl group, such as methyl, ethyl, propyl or isopropyl, in particular methyl or ethyl.
An R, R1 or R2 aryl-C1-C4 alkyl group, wherein the alkyl moiety can be straight or branched, is for example phenyl-C1-C4 alkyl, preferably benzyl or phenylethyl, wherein the phenyl ring can be optionally substituted with one to three substituents independently selected from hydroxy, C1-C4 alkoxy, for example methoxy, ethoxy or propoxy; thio, C1-C4 alkyl-thio, for example methylthio or ethylthio; nitro, cyano, halogen, for example chlorine, bromine or iodine.
An R, R1, R2 or R3 aryl group is for example a phenyl or naphthyl group, in particular optionally substituted phenyl with one to three substituents independently selected from hydroxy, alkoxy-C1-C4, for example methoxy, ethoxy or propoxy; thio, C1-C4 alkyl-thio, for example methylthio or ethylthio; nitro, cyano and halogen, for example chlorine, bromine or iodine.
In a compound of formula (II), when X is —OR, R is preferably hydrogen, a C1-C4 alkyl or —SO3H group, and when X is —NR1R2 then R1 and R2 are preferably hydrogen.
“Compound of formula (II)” means both the compound of formula (II) as such and a salt or hydrated form thereof.
A salt of a compound of formula (II) is for example an addition salt with a mineral or organic acid, such as hydrochloric, hydrobromic, sulfuric, phosphoric, acetic, oxalic, fumaric, methanesulfonic or ethanesulfonic acid, preferably hydrochloric or sulphuric acid, in particular hydrochloric acid. A compound (II) can be used also in a hydrated form, for example hydrazine hydrate.
The stoichiometric ratio of the compound (II) to a compound (I), as defined above, ranges from 0.5 to 10, preferably from 1 to 5.
The reaction between a compound (I) and a compound (II), as defined above, can be optionally carried out in the presence of solvent. Said solvent is preferably an organic solvent or mixtures thereof with water. Typically, an aromatic hydrocarbon, such as toluene or xylene; a chlorinated solvent, such as dichloromethane, dichloroethane, tetrachloroethylene, chlorobenzene or dichlorobenzene; an ester solvent, such as ethyl acetate, isopropyl acetate or butyl acetate; an ether solvent, such as tetrahydrofuran, dioxane, ethyl ether or butyl ether; an alcoholic solvent such as methanol, ethanol, isopropanol; a dipolar aprotic solvent such as acetonitrile, dimethylformamide, dimethylacetamide, dimethylsulfoxide or N-methylpyrrolidone; or a mixture of said organic solvents and/or water. Particularly preferred are methanol, ethanol or a mixture of ethanol and water.
The reaction can be carried out at a temperature ranging from about 0° C. to the reflux temperature of the reaction mixture, preferably from about 30° C. to the reflux temperature.
Furthermore, the reaction can be optionally carried out in the presence of a basic agent, for example an organic or inorganic base. Said basic agent serves to neutralize the acidity formed during the substitution reaction with chlorine of the compound (I) and moreover, if necessary, to deprotect the compound of formula (II) if present in the salified form. Examples of organic or inorganic bases are trisubstituted amines, in particular triethylamine or diisopropylethylamine, sodium acetate or potassium carbonate.
If necessary, the reaction with a reducing agent can be carried out using an agent selected from, for example, tin(II) chloride, zinc in hydrochloric acid, sodium thiosulfate, potassium iodide, thiourea and Pd on carbon together with a hydrogen donor, such as sodium formate, ammonium formate, potassium formate, formic acid, cyclohexene or limonene; or a derivative of formula (IIa) NH2—X′, or a salt or hydrated form thereof, wherein X′ is NH2 or OR′, in which R′ is hydrogen, C1-C4 alkyl or SO3H, preferably hydrogen.
A salt of a compound of formula (IIa) or a hydrated form thereof are the same as reported above in connection with a compound of formula (II).
The reaction between a compound (I) and a compound (II), in fact, can optionally be carried out stepwise, namely comprising the formation of a compound (III) or (IlIa),
wherein X has the meanings defined above; and Y is —O— or —NH—; and following reduction.
The reaction between a compound (I) and a compound (II) to afford a compound (III) or (IIIa) can be carried out analogously to what reported above.
The reduction of a compound (III) or (IIIa), which can optionally be isolated, to give Imiquimod, can be carried out using a reducing agent as defined above, such as zinc in hydrochloric acid, sodium thiosulfate or Pd/C in the presence of sodium formate as a hydrogen donor.
When in a compound (II) X is different from —OH, then its reaction with a compound (I) is preferably carried out stepswise and the resulting compound (III), in which X is different from —OH, is reduced by means of a reducing agent as defined above, preferably selected from tin(II) chloride, zinc in hydrochloric acid, sodium thiosulfate, potassium iodide, thiourea or Pd/C together with sodium formate as hydrogen donor.
More preferably, when in a compound of formula (III) X is —OR, and R is different from hydrogen, the reducing agent is selected from zinc in hydrochloric acid, sodium thiosulfate, potassium iodide, thiourea; whereas when X is —NH2, the reducing agent is Pd/C together with sodium formate.
The reduction reaction can be carried out adding the reducing agent to the reaction mixture containing the derivative (III) or (IIIa), or preferably directly reacting the compound (I) with a compound (II) in the presence of the reducing agent.
The compounds (III) and (IIIa), as defined above, are novel and are a further object of the invention.
Preferred examples of compounds (III) and (IIIa) are:
The following examples illustrate the invention.
A round-bottom three-necked flask equipped with condenser, magnetic stirrer, thermometer, is loaded with 4-chloro-1-isobutyl-1H-imidazo[4,5-c]quinoline (5.0 g, 0.019 mol), O-methyl hydroxylamine hydrochloride (3.2 g, 0.038 mol), sodium acetate (3.1 g, 0.038 mol), and an ethanol/water 2:1 v/v mixture (60 ml). The resulting mixture is then refluxed. After 14 hours, a 30% NaOH aqueous solution is added to pH 9 and the mixture is extracted with methylene chloride (3×50 ml). The combined organic phases are dried over sodium sulfate and evaporated to a residue. The resulting white solid is dried under vacuum at 50° C. Weight=4.35 g; Yield=75%.
1HNMR (300 M Hz, DMSO-d6): δ (ppm) 8.16 (s, 1H), 7.82 (d, 1H, J=8.2 Hz), 7.80 (d, 1H, J=8.2 Hz), 7.40 (t, 1H, J=8.2 Hz), 7.22 (t, 1H, J=8.2 Hz), 4.35 (d, 2H, J=7 Hz), 3.85 (s, 3H), 2.05 (m, 1H), 0.88 (d, 6H, J=7 Hz).
A round-bottom three-necked flask equipped with condenser, magnetic stirrer, thermometer, is loaded with O-hydroxylamino sulfonic acid (4.8 g, 0.042 mol), methanol (30 ml), sodium acetate (3.1 g, 0.038 mol) and finally 4-chloro-1-isobutyl-1H-imidazo[4,5-c]quinoline (10.0 g, 0.038 mol). The mixture is heated to 40° C. and left under stirring at this temperature for 24 hours. After completion of the reaction, the precipitate is filtered with suction and washed with water, then dried under vacuum at 50° C. to obtain a white solid weighing 9.5 g (yield=74%).
1HNMR (300 M Hz, DMSO-d6): δ (ppm) 8.7 (s, 1H), 8.16 (d, 1H, J=8.2 Hz), 8.07 (d, 1H, J=8.2 Hz), 7.62 (t, 1H, J=8.2 Hz), 7.48 (t, 1 H, J=8.2 Hz), 4.9 (bs, 1H), 4.45 (d, 2H, J=8 Hz), 3.15 (s, 1H), 2.13 (m, 1H), 0.89 (d, 6H, J=8 Hz).
A round-bottom three-necked flask equipped with condenser, magnetic stirrer, thermometer, is loaded with N-(1-isobutyl-1H-imidazo[4,5-c]quinolin-4-yl)-O-methyl-hydroxylamine (0.2 g, 0.74 mmol) and ethanol (15 ml). 37% HCl (1 ml) and zinc powder (48 mg, 0.74 mmol) are added under stirring. After stirring for one hour at room temperature the reaction is completed. The mixture is concentrated to half the volume, alkalinised with 50% w/w NaOH to pH 9-10 and left under stirring for 30 minutes. The resulting solid is filtered and dried under vacuum in a static dryer at 50° C. (0.12 g, yield 70%).
1HNMR (300 M Hz, DMSO-d6): δ (ppm): 8.16 (s, 1H), 8.0 (d, 1H, J=8.2 Hz), 7.61 (d, 1H, J=8.2 Hz), 7.42 (t, 1H, J=8.2 Hz), 7.26 (t, 1H, J=8.2 Hz), 6.54 (bs, 2H), 4.39 (d, 2H, J=7.5 Hz), 2.18 (m, 1H), 0.91 (d, 6H, J=7.5 Hz).
A round-bottom three-necked flask equipped with condenser, magnetic stirrer, thermometer, is loaded with 4-chloro-1-isobutyl-1H-imidazo[4,5-c]quinoline (5.0 g, 0.019 mol), hydroxylamine hydrochloride (2.6 g, 0.038 mol), sodium acetate (3.1 g, 0.038 mol), an ethanol/water 2:1 v/v mixture (60 ml). The reaction mixture is refluxed for 12 hours then left to cool at room temperature. The precipitated solid (3 g, 0.010 mol) is filtered with suction and dried under vacuum at 50° C. to constant weight. The resulting solid is then dissolved in water (6 ml) and added with sodium acetate (1 g, 0.012 mol). The precipitated product is filtered and dried under vacuum in a static dryer at 50° C. Weight=2.4 g, Yield 52%.
A round-bottom three-necked flask equipped with condenser, magnetic stirrer, thermometer, is loaded with 4-chloro-1-isobutyl-1H-imidazo[4,5-c]quinoline (5.0 g, 0.019 mol), hydrazine hydrate (3.8 g, 0.076 mol), ethanol (20 ml). The mixture is refluxed for 3 hours then left to cool at room temperature, diluted with 10 ml of a 15% ammonia aqueous solution. The precipitated solid is filtered with suction and dried under vacuum at 50° C., thereby obtaining 4.5 g of N-(1-isobutyl-1H-imidazo[4,5-c]quinolin-4-yl)-hydrazine in 92% molar yield.
1HNMR (300 M Hz, DMSO-d6): δ (ppm): 8.19 (s, 1H), 7.98 (d, 1H, J=8.1 Hz), 7.70 (d, 1H, J=8.1 Hz), 7.44 (t, 1H, J=8.1 Hz), 7.27 (t, 1H, J=8.1 Hz), 4.37 (d, 2H, J=7.5 Hz), 2.15 (m, 1H), 0.88 (d, 6H, J=6.6 Hz).
Following the same procedure, using 0.009 mol of hydrazine hydrate, N,N′-Bis-(1-isobutyl-1H-imidazo[4,5-c]quinolin-4-yl)-hydrazine is obtained.
A round-bottom three-necked flask equipped with condenser, magnetic stirrer, thermometer, is loaded with N-(1-isobutyl-1H-imidazo[4,5-c]quinolin-4-yl)-hydrazine (4.5 g, 0.018 mol), water (40 ml) 37% hydrochloric acid (1.8 g, 0.018 mol), 10% Pd-C (humid, 50% of water) (3.8 g, 0.0018 mol) and sodium formate (4.9 g 0.072 mol). The mixture is refluxed for 84 hours then left to cool at room temperature, diluted with 10 ml of a 5% HCl solution to pH<2; filtered through Celite and alkalinised with an ammonia aqueous solution to pH>8. The precipitated solid is filtered with suction and dried under vacuum in a static dryer at 50° C., thereby obtaining 4.3 g in 98% molar yield.
| Number | Date | Country | Kind |
|---|---|---|---|
| MI2004A001282 | Jun 2004 | IT | national |
