JP2006265207A - Method for producing heterocyclic compound - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a method for producing an anilino group-substituted heterocyclic compound in a high yield in high purity and at a low cost. <P>SOLUTION: This method for producing the anilino group-substituted heterocyclic compound is characterized by reacting a heterocyclic compound having at least one releasing group in the molecule with an aniline derivative in the presence of a Lewis acid. <P>COPYRIGHT: (C)2007,JPO&INPIT

Description

  The present invention relates to a method for producing a heterocyclic compound.

  The heterocyclic compound represented by the following general formula (3) is a useful compound as an intermediate for the synthesis of functional compounds such as photographic additives, sensitizing dyes, dyes, electronic materials, and medical and agricultural chemicals.

(In the formula, Het represents a heterocyclic ring, n represents an integer of 1, 2 or 3, and R ₁ to R ₆ each independently represents a hydrogen atom or a substituent.)

As a general synthesis method of the heterocyclic compound represented by the general formula (3) (hereinafter referred to as a heterocyclic compound substituted with an anilino group), (A) a heterocyclic compound substituted with an amino group and halogen And nucleophilic substitution reaction of a heterocyclic compound having a leaving group and an aniline derivative. These typical nucleophilic substitution reactions are described in Non-Patent Document 1 and Non-Patent Document 2. Among these, addition of a copper catalyst (Ullmann reaction) and addition of a palladium catalyst have long been known as versatile synthesis methods.
The nucleophilic substitution reaction of the type (B) is highly reactive when an electron withdrawing group is substituted on the heterocyclic compound or when an electron donating group is substituted on the aniline derivative. However, even in an electronically advantageous situation, if a sterically bulky group is substituted in the vicinity of the reaction point, there is a problem that the reactivity is extremely lowered.
Hiroshi Yamanaka et al., “Chemistry of Heterocyclic Compounds”, Kodansha, Inc., April 1, 1988 Hitomi Suzuki “Organic Chemistry Course 2, Organic Reaction II, Aromatic Compounds”, Maruzen Co., Ltd., June 15, 1984

  Thus, regarding the nucleophilic substitution reaction between the heterocyclic compound having a leaving group and the aniline derivative, particularly when the ortho position of the aniline derivative is substituted with a sterically bulky group, the reactivity is greatly reduced. I understood that. Accordingly, an object of the present invention is to provide a method for producing a heterocyclic compound substituted with an anilino group represented by the general formula (3) at high yield, high purity and low cost.

As a result of investigations to overcome these conventional problems, the present inventors have found that a nucleophilic substitution reaction between a heterocyclic compound having a leaving group and an aniline derivative is accelerated in the presence of a Lewis acid, The target heterocyclic compound substituted with an anilino group can be obtained in high yield, high purity and low cost.
The present invention is as follows.

  1) A heterocyclic compound represented by the following general formula (1) having at least one leaving group in the molecule and an aniline derivative represented by the following general formula (2) in the presence of a Lewis acid A process for producing a heterocyclic compound represented by the following general formula (3), wherein

(In the formula, Het represents a heterocyclic ring, X ₁ represents a leaving group, n represents an integer of 1, 2 or 3, and R ₁ to R ₆ each independently represent a hydrogen atom or a substituent. R ₁ and R ₆ , R ₁ and R ₂ , R ₂ and R ₃ , R ₃ and R ₄ , and R ₄ and R ₅ may be bonded to each other to form a cyclic structure.)

  2) The method according to 1) above, wherein the Het is a nitrogen-containing heterocycle.

3) The method according to 2) above, wherein the Het is a pyridine ring.
4) The production method according to 1) above, wherein the heterocyclic compound represented by the general formula (1) is a heterocyclic compound represented by the general formula (4).

(Wherein X ₂ represents a leaving group, R ₈ represents a hydrogen atom, a substituted or unsubstituted alkyl group or a substituted or unsubstituted aryl group, and R ₇ and R ₉ independently represent a hydrogen atom or an electron Represents an attractive group.)

  5) The production method according to 4) above, wherein the heterocyclic compound represented by the general formula (1) is a heterocyclic compound represented by the following compound (5).

6) The production method according to any one of 1) to 5) above, wherein R ₁ and R ₅ in the general formula (2) are substituted or unsubstituted alkyl groups having 2 or more carbon atoms.
7) The aniline derivative represented by the general formula (2) is 2,6-diethylaniline or 2,6-diethyl-4-methylaniline. The manufacturing method as described.

  8) The production method according to any one of 1) to 7) above, wherein the Lewis acid is iron (III) chloride or zinc (II) chloride.

  9) The production method according to any one of 1) to 8) above, wherein a catalytic amount of a Lewis acid is used.

  According to the method for producing a heterocyclic compound substituted with an anilino group of the present invention, a heterocyclic compound having one or more anilino groups represented by the general formula (3), particularly a steric compound at the ortho position of the anilino group. A pyridine ring derivative having an anilino group substituted with a bulky group can be obtained in high yield, high purity and low cost.

Hereinafter, the manufacturing method of the heterocyclic compound substituted by the anilino group of this invention is demonstrated.
First, the heterocyclic compound substituted with an anilino group produced by the production method of the present invention will be described in detail.
The heterocyclic compound substituted by the anilino group obtained by the production method of the present invention is a compound represented by the general formula (3).

In general formula (2) and general formula (3), R < ₁ > -R < ₆ > represents a hydrogen atom or a substituent, and the following groups are mentioned as a substituent.
For example, halogen atom, alkyl group (including cycloalkyl group and bicycloalkyl group), alkenyl group (including cycloalkenyl group and bicycloalkenyl group), alkynyl group, aryl group, heterocyclic group, cyano group, hydroxyl group, nitro Group, carboxyl group, alkoxy group, aryloxy group, silyloxy group, heterocyclic oxy group, acyloxy group, carbamoyloxy group, alkoxycarbonyloxy group, aryloxycarbonyloxy group, amino group, acylamino group, aminocarbonylamino group, alkoxy Carbonylamino group, aryloxycarbonylamino group, sulfamoylamino group, alkyl or arylsulfonylamino group, mercapto group, alkylthio group, arylthio group, heterocyclic thio group, sulfamoyl group, sulfo group Alkyl or arylsulfinyl group, alkyl or arylsulfonyl group, acyl group, aryloxycarbonyl group, alkoxycarbonyl group, carbamoyl group, aryl or heterocyclic azo group, imide group, phosphino group, phosphinyl group, phosphinyloxy group, phosphine group Examples include a finylamino group and a silyl group.

  More specifically, examples of the halogen atom include a fluorine atom, a chlorine atom, a bromine atom, and an iodine atom.

  Examples of the alkyl group include linear, branched, and cyclic substituted or unsubstituted alkyl groups, and also include cycloalkyl groups, bicycloalkyl groups, and tricyclo structures having many ring structures. An alkyl group (for example, an alkyl group of an alkylthio group) in the substituents described below also represents such an alkyl group. Specifically, the alkyl group is preferably an alkyl group having 1 to 30 carbon atoms, such as a methyl group, ethyl group, n-propyl group, isopropyl group, t-butyl group, n-octyl group, eicosyl group, A 2-chloroethyl group, a 2-cyanoethyl group, a 2-ethylhexyl group, and the like. The cycloalkyl group is preferably a substituted or unsubstituted cycloalkyl group having 3 to 30 carbon atoms, such as a cyclohexyl group or a cyclopentyl group. 4-n-dodecylcyclohexyl group and the like, and the bicycloalkyl group is preferably a substituted or unsubstituted bicycloalkyl group having 5 to 30 carbon atoms, that is, a bicyclic alkane having 5 to 30 carbon atoms to a hydrogen atom. A monovalent group such as a bicyclo [1,2,2] heptan-2-yl group, B [2,2,2] octan-3-yl group.

Examples of the alkenyl group include linear, branched, and cyclic substituted or unsubstituted alkenyl groups, and include cycloalkenyl groups and bicycloalkenyl groups. Specifically, the alkenyl group is preferably a substituted or unsubstituted alkenyl group having 2 to 30 carbon atoms, such as a vinyl group, an allyl group, a prenyl group, a geranyl group, an oleyl group, and the like. Is preferably a substituted or unsubstituted cycloalkenyl group having 3 to 30 carbon atoms, that is, a monovalent group obtained by removing one hydrogen atom of a cycloalkene having 3 to 30 carbon atoms, such as 2-cyclopentene-1 -Yl group, 2-cyclohexen-1-yl group and the like. As the bicycloalkenyl group, a substituted or unsubstituted bicycloalkenyl group, preferably a substituted or unsubstituted bicycloalkenyl group having 5 to 30 carbon atoms, That is, a monovalent group obtained by removing one hydrogen atom of a bicycloalkene having one double bond, for example, bicyclo [ , 2,1] hept-2-en-1-yl group, a bicyclo [2,2,2] oct-2-en-4-yl group and the like.
The alkynyl group is preferably a substituted or unsubstituted alkynyl group having 2 to 30 carbon atoms, such as an ethynyl group, a propargyl group, or a trimethylsilylethynyl group.

The aryl group is preferably a substituted or unsubstituted aryl group having 6 to 30 carbon atoms, such as a phenyl group, a p-tolyl group, a naphthyl group, an m-chlorophenyl group, an o-hexadecanoylaminophenyl group, and the like. Can be mentioned.
The heterocyclic group is preferably a monovalent group obtained by removing one hydrogen atom from a 5- or 6-membered substituted or unsubstituted aromatic or non-aromatic heterocyclic compound, and more preferably a carbon number. Examples thereof include 3 to 30 5- or 6-membered aromatic heterocyclic groups such as a 2-furyl group, a 2-thienyl group, a 2-pyrimidinyl group, and a 2-benzothiazolyl group.
The alkoxy group is preferably a substituted or unsubstituted alkoxy group having 1 to 30 carbon atoms, such as a methoxy group, an ethoxy group, an isopropoxy group, a t-butoxy group, an n-octyloxy group, or a 2-methoxyethoxy group. Etc.
In the present specification, “alkoxy” has the same meaning as “alkyloxy”, and alkyl in alkyloxy has the same meaning as described above.

The aryloxy group is preferably a substituted or unsubstituted aryloxy group having 6 to 30 carbon atoms, such as a phenoxy group, 2-methylphenoxy group, 4-t-butylphenoxy group, 3-nitrophenoxy group, 2 -Tetradecanoylaminophenoxy group etc. are mentioned.
Preferred examples of the heterocyclic oxy group include substituted or unsubstituted heterocyclic oxy groups having 2 to 30 carbon atoms, such as a 1-phenyltetrazole-5-oxy group and a 2-tetrahydropyranyloxy group.
The acyloxy group is preferably a formyloxy group, a substituted or unsubstituted alkylcarbonyloxy group having 2 to 30 carbon atoms, a substituted or unsubstituted arylcarbonyloxy group having 6 to 30 carbon atoms, such as an acetyloxy group, Examples include a pivaloyloxy group, a stearoyloxy group, a benzoyloxy group, and a p-methoxyphenylcarbonyloxy group.
The carbamoyloxy group is preferably a substituted or unsubstituted carbamoyloxy group having 1 to 30 carbon atoms, such as N, N-dimethylcarbamoyloxy group, N, N-diethylcarbamoyloxy group, morpholinocarbonyloxy group, N , N-di-n-octylaminocarbonyloxy group, Nn-octylcarbamoyloxy group and the like.

The alkoxycarbonyloxy group is preferably a substituted or unsubstituted alkoxycarbonyloxy group having 2 to 30 carbon atoms, such as a methoxycarbonyloxy group, an ethoxycarbonyloxy group, a t-butoxycarbonyloxy group, or an n-octylcarbonyloxy group. Etc.
The aryloxycarbonyloxy group is preferably a substituted or unsubstituted aryloxycarbonyloxy group having 7 to 30 carbon atoms, such as phenoxycarbonyloxy group, p-methoxyphenoxycarbonyloxy group, pn-hexadecyloxy. Examples include phenoxycarbonyloxy group.
The amino group includes an alkylamino group, an arylamino group, and a heterocyclic amino group, preferably an amino group, a substituted or unsubstituted alkylamino group having 1 to 30 carbon atoms, a substituted or unsubstituted group having 6 to 30 carbon atoms. Examples of the substituted anilino group include a methylamino group, a dimethylamino group, an anilino group, an N-methyl-anilino group, and a diphenylamino group.
The acylamino group is preferably a formylamino group, a substituted or unsubstituted alkylcarbonylamino group having 1 to 30 carbon atoms, a substituted or unsubstituted arylcarbonylamino group having 6 to 30 carbon atoms, such as an acetylamino group, Examples include pivaloylamino group, lauroylamino group, benzoylamino group, 3,4,5-tri-n-octyloxyphenylcarbonylamino group, and the like.

The aminocarbonylamino group is preferably a substituted or unsubstituted aminocarbonylamino group having 1 to 30 carbon atoms, such as a carbamoylamino group, an N, N-dimethylaminocarbonylamino group, or an N, N-diethylaminocarbonylamino group. And a morpholinocarbonylamino group.
The alkoxycarbonylamino group is preferably a substituted or unsubstituted alkoxycarbonylamino group having 2 to 30 carbon atoms, such as a methoxycarbonylamino group, an ethoxycarbonylamino group, a t-butoxycarbonylamino group, or an n-octadecyloxycarbonylamino group. Group, N-methyl-methoxycarbonylamino group and the like.
The aryloxycarbonylamino group is preferably a substituted or unsubstituted aryloxycarbonylamino group having 7 to 30 carbon atoms, such as phenoxycarbonylamino group, p-chlorophenoxycarbonylamino group, mn-octyloxyphenoxy. A carbonylamino group etc. are mentioned.
The sulfamoylamino group is preferably a substituted or unsubstituted sulfamoylamino group having 0 to 30 carbon atoms, such as a sulfamoylamino group, N, N-dimethylaminosulfonylamino group, Nn- Examples include octylaminosulfonylamino group.

The alkyl or arylsulfonylamino group is preferably a substituted or unsubstituted alkylsulfonylamino group having 1 to 30 carbon atoms, a substituted or unsubstituted arylsulfonylamino group having 6 to 30 carbon atoms, such as a methylsulfonylamino group. Butylsulfonylamino group, phenylsulfonylamino group, 2,3,5-trichlorophenylsulfonylamino group, p-methylphenylsulfonylamino group, and the like.
The alkylthio group is preferably a substituted or unsubstituted alkylthio group having 1 to 30 carbon atoms, such as a methylthio group, an ethylthio group, and an n-hexadecylthio group.
Preferred examples of the arylthio group include substituted or unsubstituted arylthio groups having 6 to 30 carbon atoms such as a phenylthio group, a p-chlorophenylthio group, and an m-methoxyphenylthio group.
Preferred examples of the heterocyclic thio group include substituted or unsubstituted heterocyclic thio groups having 2 to 30 carbon atoms such as a 2-benzothiazolylthio group and a 1-phenyltetrazol-5-ylthio group.
The sulfamoyl group is preferably a substituted or unsubstituted sulfamoyl group having 0 to 30 carbon atoms, such as N-ethylsulfamoyl group, N- (3-dodecyloxypropyl) sulfamoyl group, N, N-dimethylsulfuryl group. Examples include a famoyl group, an N-acetylsulfamoyl group, an N-benzoylsulfamoyl group, and an N- (N′-phenylcarbamoyl) sulfamoyl group.

The alkyl or arylsulfinyl group is preferably a substituted or unsubstituted alkylsulfinyl group having 1 to 30 carbon atoms, a substituted or unsubstituted arylsulfinyl group having 6 to 30 carbon atoms, such as a methylsulfinyl group, an ethylsulfinyl group, phenyl. Examples thereof include a sulfinyl group and a p-methylphenylsulfinyl group.
The alkyl or arylsulfonyl group is preferably a substituted or unsubstituted alkylsulfonyl group having 1 to 30 carbon atoms, a substituted or unsubstituted arylsulfonyl group having 6 to 30 carbon atoms, such as a methylsulfonyl group, an ethylsulfonyl group, a phenyl group. A sulfonyl group, p-methylphenylsulfonyl group, etc. are mentioned.
The acyl group is preferably a formyl group, a substituted or unsubstituted alkylcarbonyl group having 2 to 30 carbon atoms, a substituted or unsubstituted arylcarbonyl group having 7 to 30 carbon atoms, a substituted or unsubstituted group having 2 to 30 carbon atoms. Heterocyclic carbonyl groups bonded to carbonyl groups at substituted carbon atoms, for example, acetyl, pivaloyl, 2-chloroacetyl, stearoyl, benzoyl, pn-octyloxyphenylcarbonyl, 2-pyridyl Examples thereof include a carbonyl group and a 2-furylcarbonyl group.
The aryloxycarbonyl group is preferably a substituted or unsubstituted aryloxycarbonyl group having 7 to 30 carbon atoms, such as phenoxycarbonyl group, o-chlorophenoxycarbonyl group, m-nitrophenoxycarbonyl group, pt- A butylphenoxycarbonyl group etc. are mentioned.

Preferred examples of the alkoxycarbonyl group include substituted or unsubstituted alkoxycarbonyl groups having 2 to 30 carbon atoms such as a methoxycarbonyl group, an ethoxycarbonyl group, a t-butoxycarbonyl group, and an n-octadecyloxycarbonyl group.
The carbamoyl group is preferably a substituted or unsubstituted carbamoyl group having 1 to 30 carbon atoms, such as a carbamoyl group, an N-methylcarbamoyl group, an N, N-dimethylcarbamoyl group, or an N, N-di-n-octyl group. Examples thereof include a carbamoyl group and an N- (methylsulfonyl) carbamoyl group.
The aryl or heterocyclic azo group is preferably a substituted or unsubstituted arylazo group having 6 to 30 carbon atoms, a substituted or unsubstituted heterocyclic azo group having 3 to 30 carbon atoms, such as phenylazo, p-chlorophenylazo, 5-ethylthio-1,3,4-thiadiazol-2-ylazo and the like.

Preferred examples of the imide group include an N-succinimide group and an N-phthalimide group.
Preferred examples of the phosphino group include substituted or unsubstituted phosphino groups having 2 to 30 carbon atoms, such as a dimethylphosphino group, a diphenylphosphino group, and a methylphenoxyphosphino group.
The phosphinyl group is preferably a substituted or unsubstituted phosphinyl group having 2 to 30 carbon atoms, such as a phosphinyl group, a dioctyloxyphosphinyl group, a diethoxyphosphinyl group, and the like.
Preferred examples of the phosphinyloxy group include substituted or unsubstituted phosphinyloxy groups having 2 to 30 carbon atoms such as a diphenoxyphosphinyloxy group and a dioctyloxyphosphinyloxy group.
The phosphinylamino group is preferably a substituted or unsubstituted phosphinylamino group having 2 to 30 carbon atoms, such as a dimethoxyphosphinylamino group or a dimethylaminophosphinylamino group.
The silyl group is preferably a substituted or unsubstituted silyl group having 3 to 30 carbon atoms, such as trimethylsilyl, t-butyldimethylsilyl, phenyldimethylsilyl and the like.

  Among the above substituents, those having a hydrogen atom may be substituted with the above substituent. Examples of such a substituent include an alkylcarbonylaminosulfonyl group, an arylcarbonylaminosulfonyl group, an alkylsulfonylaminocarbonyl group, and an arylsulfonylaminocarbonyl group. Examples thereof include a methylsulfonylaminocarbonyl group, a p-methylphenylsulfonylaminocarbonyl group, an acetylaminosulfonyl group, and a benzoylaminosulfonyl group.

R ₁ and R ₅ are preferably a halogen atom, an alkyl group, an aryl group, a carboxyl group, an alkoxy group, an acylamino group, an alkylthio group, or an arylthio group, particularly preferably an alkyl group, An unsubstituted alkyl group is most preferred.
R ₂ , R ₃ and R ₄ are preferably a hydrogen atom, a halogen atom, an alkyl group, an aryl group, a hydroxyl group, a carboxyl group, an alkoxy group, an acylamino group, an alkylthio group, an arylthio group or a sulfo group, particularly preferably , A hydrogen atom or an alkyl group.
R ₆ is preferably a hydrogen atom, an alkyl group, an aryl group, an acyl group, or an alkoxycarbonyl group, and particularly preferably a hydrogen atom.
Specific examples of the aniline derivative represented by the general formula (2) include 2,6-diethylaniline and 2,6-diethyl-4-methylaniline.

In the general formulas (1) and (3), Het represents a heterocyclic ring (excluding xanthene). In the specification of the present application, a heterocyclic ring means an element containing oxygen, sulfur, nitrogen or the like called a hetero atom in addition to a carbon atom as an element constituting the ring. Examples of the heterocyclic ring include pyrrole, furan, thiophene, benzopyrrole, benzofuran, benzothiophene, pyrazole, isoxazole, isothiazole, benzopyrazole, benzisoxazole, benzoisothiazole, imidazole, oxazole, thiazole, benzimidazole, benzo Examples include oxazole, benzothiazole, pyridine, quinoline, isoquinoline, pyridazine, pyrimidine, pyrazine, phthalazine, quinazoline, quinoxaline, acridine, carbazole, purine, pteridine, thiadiazole, triazole, tetrazole and the like.
Het is preferably a nitrogen-containing heterocyclic ring. The nitrogen-containing heterocycle refers to a heterocycle containing nitrogen as an element constituting the ring. Examples of the nitrogen-containing heterocycle include pyrrole, benzopyrrole, imidazole, benzimidazole, pyridine, quinoline, pyridazine, pyrimidine, pyrazine and the like. Preferred nitrogen-containing heterocycles are imidazole, pyridine, and pyridazine, and particularly preferred is pyridine.

  In General Formula (1) and General Formula (3), n represents an integer value of 1, 2, or 3. n is preferably 1 or 2, particularly preferably 2.

In the general formula (1), X ₁ represents a leaving group. Examples of the leaving group include a halogen atom, a nitro group, an alkyl or arylsulfonyloxy group, an alkyl or arylsulfinyloxy group, an alkyl or arylthio group, an alkoxy group, an aryloxy group, a quaternary alkyl ammonium salt, and a diazonium salt. The leaving group is preferably a halogen atom or an alkyl or arylsulfonyloxy group, particularly preferably a halogen atom.

  A preferable form of the general formula (1) is represented by the following general formula (4).

In the general formula (4), X ₂ represents a leaving group, R ₈ represents a hydrogen atom, a substituted or unsubstituted alkyl group or a substituted or unsubstituted aryl group, and R ₇ and R ₉ are each independently hydrogen. Represents an atomic or electron withdrawing group.

X ₂ in the general formula (4) has the same meaning as X _{1 in the} general formula (1).
R ₈ represents a hydrogen atom, a substituted or unsubstituted alkyl group or a substituted or unsubstituted aryl group, preferably a substituted or unsubstituted alkyl group, particularly preferably a methyl group.

R ₇ and R ₉ each independently represent a hydrogen atom or an electron-withdrawing group, and the electron-withdrawing group is a substituent having an electron-withdrawing property due to an electronic effect. If the Hammett's substituent constant σp value, which is a measure of the property and electron donating property, is used, it is a substituent having a large σp value. Examples include a cyano group, a nitro group, a halogen atom, a sulfo group, a trifluoromethyl group, a carbonyl group, and a carboxyalkyl group. Hammett's substituent constant σp value will be described briefly. Hammett's rule is an empirical rule proposed by LP Hammett in 1935 to quantitatively discuss the influence of substituents on the reaction or equilibrium of benzene derivatives, which is widely accepted today. Substituent constants determined by Hammett's rule include σp value and σm value, and these values can be found in many general books. For example, JADean edition “Lange's Handbook of Chemistry” 12th edition 1979 (Mc Graw-Hill), “Chemicals” special edition, 122, 96-103, 1979 (Nankodo).
R ₇ and R ₉ are preferably a hydrogen atom, a cyano group, a nitro group, an acyl group, an alkoxycarbonyl group, or a carbamoyl group, and particularly preferably a hydrogen atom or a cyano group.

    The most preferable form of the general formula (1) is represented by the following compound (5).

As a substituent for R _{1 to} R _{6 in} the general formula (2) and general formula (3), a ballast group used in a photographic material and an adsorbing group to a silver salt and water-solubility are imparted. It may have a group, may be polymerized with each other to form a polymer, or may be bonded to each other to form a bis type, a tris type, or a tetrakis type. R ₁ and R ₆ , R ₁ and R ₂ , R ₂ and R ₃ , R ₃ and R ₄ , and R ₄ and R ₅ may be bonded to each other to form a cyclic structure.

  Next, although the preferable compound example of General formula (3) is given as a specific example, this invention is not limited to these.

  The heterocyclic compound substituted with the anilino group may exist as a tautomer depending on the type of the substituent. Any tautomer in pure form, any mixture of tautomers is encompassed by the compounds of the present invention.

  The heterocyclic compound substituted with the anilino group includes those accompanied with a counter salt by the synthesis process or isolation method. Any salt may be used, but examples thereof include halide ions, sulfate ions, nitrate ions, carbonate ions, sulfonate ions, phosphate ions, acetate ions, metal ions, and ammonium ions. Depending on the structure, an inner salt may be formed.

Next, a method for producing the compound represented by the general formula (3) (a method for producing a heterocyclic compound substituted with an anilino group of the present invention) will be described in detail.
In the production method of the present invention, a heterocyclic compound having one or more leaving groups represented by the general formula (1) is reacted with an aniline derivative represented by the general formula (2) in the presence of a Lewis acid. It is characterized by.

The Lewis acid used in the production method of the present invention refers to a substance having an empty orbit capable of receiving at least one electron pair. Examples of the Lewis acid include aluminum bromide (III), aluminum chloride (III), gallium chloride (III), iron chloride (III), antimony chloride (V), tin chloride (IV), titanium chloride (IV), Metals such as zinc chloride (II), boron fluoride (III), boron chloride (III), copper (II) trifluoromethanesulfonate, zinc (II) trifluoromethanesulfonate, diphosphorus pentoxide, Mo (CO) ₆ Examples thereof include a carbonyl complex, a fluororesin solid acid catalyst represented by Nafion-H (trade name of Du Pont), and a lanthanoid trifluoromethanesulfonate complex represented by scandium (III) trifluoromethanesulfonate. The Lewis acid is preferably zinc (II) chloride or iron (III) chloride.

  The amount of Lewis acid used can be selected as appropriate, but it is preferably used in a catalytic amount, and usually about 0.001 to 3 mol can be used per 1 mol of the compound represented by the general formula (1). More preferably, it is about 0.01-1 mol, Especially preferably, about 0.05-0.3 mol can be used. Here, the amount of catalyst means that the number of moles of Lewis acid used is smaller than the number of moles of general formula (1) used.

  Although the usage-amount of the aniline derivative represented by General formula (2) used for the manufacturing method of this invention can be selected suitably, it is usually 0.00 with respect to 1 mol of compounds represented by General formula (1). About 5 to 25 mol can be used, more preferably about 1 to 15 mol, and particularly preferably about 1.5 to 10 mol.

In producing the compound represented by the general formula (3), it is preferable that no solvent is used, but the reaction proceeds in the same manner even when an organic solvent is used. The type of the organic solvent can be appropriately selected according to the reaction system. For example, acetone, methyl ethyl ketone, acetonitrile, propionitrile, butyronitrile, alcohol (for example, methanol, ethanol, i-propyl alcohol, etc.), chloride, etc. Methylene, chloroform, carbon tetrachloride, dichloroethane, ethyl acetate, butyl acetate, benzene, toluene, xylene, hexane, cyclohexane, diethyl ether, tetrahydrofuran, 1,4-dioxane, N, N-dimethylformamide (DMF), N, N -Dimethylacetamide (DMAC), N, N-dimethylimidazolidinone (DMI), sulfolane, dimethyl sulfoxide (DMSO), N-methylpyrrolidone (NMP) and the like. These organic solvents may be appropriately combined and used as a mixture.
The organic solvent in the production method of the present invention is preferably tetrahydrofuran, 1,4-dioxane, DMF, DMAC, DMI, sulfolane, DMSO, or NMP, and particularly preferably DMI, sulfolane, or NMP.
The amount of the reaction solvent to be used is not particularly limited and can be appropriately selected according to the type of reaction system, etc., but usually the organic solvent is represented by mass ratio with respect to the compound represented by the general formula (1). About 0-100 times is suitable, 0-10 times are preferable, Especially preferably, it is about 0-5 times.

The reaction temperature in the production method of the present invention is not particularly limited and can be appropriately selected depending on the type of reaction system and the concentration of the compound of the reaction species, but is usually about 0 ° C to 400 ° C, preferably 50 ° C. It is -300 degreeC, Most preferably, it is 100 degreeC-250 degreeC.
Although the reaction time is not particularly limited, it is usually about 1 minute to 24 hours, preferably 30 minutes to 12 hours, particularly preferably 1 hour to 6 hours.

  The order of adding the compound represented by the general formula (1) or the general formula (2), the Lewis acid and the reaction solvent into the reaction system is arbitrary, and is not particularly limited.

  EXAMPLES Hereinafter, although an Example demonstrates this invention further, this invention is not restrict | limited to the following example. In addition, HPLC purity means the area percentage when it measures with a detection wavelength of 254 nm using a high performance liquid chromatography.

Example 1
First, the synthesis example of exemplary compound D-31 is shown.
<Synthesis Example: Synthesis Method of Exemplary Compound D-31>
3,7.4 g (0.2 mol) of 2,6-dichloro-4-methyl-3-pyridinecarbonitrile, 149.2 g (1.0 mol) of 2,6-diethylaniline, 10.6 g of anhydrous sodium carbonate (0. 1 mol), 6.82 g (0.05 mol) of anhydrous zinc chloride was added to 10.0 g of N-methylpyrrolidone, and the mixture was heated and stirred at an internal temperature of 200 to 205 ° C. for 6 hours (under a nitrogen atmosphere). The reaction solution was gradually cooled, and 100 mL of isopropanol was added dropwise over 5 minutes at an internal temperature of 130 ° C., and 200 mL of methanol was added dropwise over 10 minutes at an internal temperature of 100 ° C. This reaction solution is filtered at an internal temperature of 40 to 50 ° C. (to remove insoluble materials), 125 mL of water is added dropwise to the filtrate at room temperature, the precipitated crystals are collected by filtration, washed with 50 mL of isopropanol and 100 mL of water, and dried. Example Compound (D-31) was obtained in 60.2 g (pale yellow crystals, yield 73.0%, HPLC purity 94.8%).
¹ H-NMR (300 MHz, CDCl ₃ )
6.9-7.3 (m, 6H), 6.28 (s, 1H), 6.03 (s, 1H), 5.20 (s, 1H), 2.4-2.7 (m, 8H), 2.22 (s, 3H), 1.21 (t, J = 7.5 Hz, 6H), 1.07 (t, J = 7.5 Hz, 6H)

<Synthesis Example: Synthesis Method of Exemplary Compound D-32>
2.6.1 g (0.3 mol) of 2,6-dichloro-4-methyl-3-pyridinecarbonitrile, 244.9 g (1.5 mol) of 2,6-diethyl-4-methylaniline and anhydrous zinc chloride. 18 g (0.06 mol) was added, and the mixture was heated and stirred at an internal temperature of 200 to 205 ° C. for 6 hours (under a nitrogen atmosphere). The reaction solution was gradually cooled, and 75 mL of isopropanol was added dropwise over 20 minutes at an internal temperature of 130 ° C., and 225 mL of methanol was added dropwise over 20 minutes at an internal temperature of 100 ° C. The reaction solution was filtered at an internal temperature of 40 to 50 ° C. (to remove insoluble matter), 135 mL of water was added dropwise to the filtrate at room temperature over 15 minutes, and the precipitated crystals were collected by filtration, 75 mL of isopropanol and 225 mL of water. And dried to obtain 91.6 g (pale yellow crystals, yield 70.3%, HPLC purity 98.6%) of the exemplified compound (D-32).
¹ H-NMR (400 MHz, CDCl ₃ )
6.98 (s, 2H), 6.92 (s, 2H), 6.21 (s, 1H), 5.99 (s, 1H), 5.17 (s, 1H), 2.4-2 .7 (m, 8H), 2.35 (s, 3H), 2.32 (s, 3H), 2.20 (s, 3H), 1.18 (t, J = 7.6 Hz, 6H), 1.04 (t, J = 7.7 Hz, 6H)

<Synthesis Example: Synthesis Method of Exemplary Compound D-38>
Add 18.4 g (0.135 mol) of anhydrous zinc chloride to 252.5 g (1.35 mol) of 2,6-dichloro-4-methyl-3-pyridinecarbonitrile and 754.4 g (8.1 mol) of aniline. After heating, the mixture was heated and stirred at an external temperature of 125 ° C. (internal temperature 120 to 135 ° C.) for 1 hour, and further heated and stirred at an external temperature of 150 ° C. (internal temperature 140 to 145 ° C.) for 5 hours (nitrogen). Under atmosphere). The reaction solution was gradually cooled, 525 mL of isopropanol was added dropwise at an internal temperature of 130 ° C., 525 mL of methanol was added dropwise at an internal temperature of 90 ° C., and 3375 mL of 2.4 mol / l hydrochloric acid was added dropwise at an internal temperature of 40 ° C. The reaction mixture was stirred at room temperature for 1 hour, and the precipitated crystals were collected by filtration, washed with 3300 mL of water, dried and 337.1 g of the exemplified compound (D-38) (white crystals, yield 83.1%, HPLC purity). 99.8%).
¹ H-NMR (300 MHz, DMSO)
9.37 (s, 1H), 8.74 (s, 1H), 7.4-7.6 (m, 4H), 7.30 (t, J = 5.4 Hz, 2H), 7.14 ( t, J = 5.4 Hz, 2H), 7.06 (t, J = 5.4 Hz, 1H), 6.92 (t, J = 5.4 Hz, 1H), 6.21 (s, 1H), 2.30 (s, 3H)

(Test example)
Using the synthesis method of the exemplified compounds D-31, D-32 and D-38 shown in the above examples, the reaction was traced with and without zinc chloride (II) which is a Lewis acid. The production rates of D-31 and D-32 over the course of the reaction were determined by area (%) in HPLC measurement, and the effect of Lewis acid was tested. The detection wavelength for HPLC measurement was 254 nm.

  As shown in the above examples, according to the production method of the present invention, high yield of the heterocyclic compound substituted with the target anilino group is improved by adding the Lewis acid, especially the catalytic amount. It has been found that it can be produced at a high rate, high purity and low cost.

Claims (9)

Reaction of a heterocyclic compound represented by the following general formula (1) having at least one leaving group in the molecule with an aniline derivative represented by the following general formula (2) in the presence of a Lewis acid. A method for producing a heterocyclic compound represented by the following general formula (3):

(In the formula, Het represents a heterocyclic ring, X ₁ represents a leaving group, n represents an integer of 1, 2 or 3, and R ₁ to R ₆ each independently represent a hydrogen atom or a substituent. R ₁ and R ₆ , R ₁ and R ₂ , R ₂ and R ₃ , R ₃ and R ₄ , and R ₄ and R ₅ may be bonded to each other to form a cyclic structure.)   The method according to claim 1, wherein the Het is a nitrogen-containing heterocycle.   The method according to claim 2, wherein the Het is a pyridine ring. The manufacturing method according to claim 1, wherein the heterocyclic compound represented by the general formula (1) is a heterocyclic compound represented by the general formula (4).

(Wherein X ₂ represents a leaving group, R ₈ represents a hydrogen atom, a substituted or unsubstituted alkyl group or a substituted or unsubstituted aryl group, and R ₇ and R ₉ independently represent a hydrogen atom or an electron Represents an attractive group.) The manufacturing method according to claim 4, wherein the heterocyclic compound represented by the general formula (1) is a heterocyclic compound represented by the following compound (5).

6. The production method according to claim 1, wherein R ₁ and R ₅ in the general formula (2) are substituted or unsubstituted alkyl groups having 2 or more carbon atoms.   6. The production according to claim 1, wherein the aniline derivative represented by the general formula (2) is 2,6-diethylaniline or 2,6-diethyl-4-methylaniline. Method.   The production method according to claim 1, wherein the Lewis acid is iron (III) chloride or zinc (II) chloride.   9. A process according to any one of claims 1 to 8, characterized in that a catalytic amount of Lewis acid is used.