CN104945387B - Intermediate for preparing pyrazol formic acid derivative - Google Patents
Intermediate for preparing pyrazol formic acid derivative Download PDFInfo
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- CN104945387B CN104945387B CN201510348921.1A CN201510348921A CN104945387B CN 104945387 B CN104945387 B CN 104945387B CN 201510348921 A CN201510348921 A CN 201510348921A CN 104945387 B CN104945387 B CN 104945387B
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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Abstract
The invention relates to a compound for preparing a pyrazol formic acid derivative. The compound is shown in the formula (II). The compound is used for synthesizing an intermediate of the pyrazol formic acid derivative. The pyrazol formic acid derivative is high in reaction yield, the amount of waste gas and waste water is small, cost is low, and special reaction equipment is of no need.
Description
Technical field
The present invention relates to a kind of intermediate for preparing pyrazole carboxylic acid derivant.
Background technology
Pyrazole carboxylic acid derivant, such as 3- difluoromethyls -1- methyl isophthalic acids H- pyrazoles -4- carboxylic acids are for preparing agriculture chemicals fungicide
Key intermediate.
Document JP-2000-044541 reports, in the presence of a base, corresponding substituted pyrazolecarboxylic and carboxylic acid dialkyl esters such as sulphuric acid
Dimethyl ester, dithyl sulfate carry out N- and methylate, and obtain N- substituted pyrazolecarboxylics, then Jing series reactions obtain pyrazole carboxylic acid derivant.
But dialkyl sulfate is difficult to large-scale application due to its toxicity in big factory.
Chinese patent CN101044116A replaces the dialkyl sulfate of severe toxicity using trialkylphosphate, however it is necessary that
At 180-200 DEG C of high temperature, 18-24 hours are reacted, and post processing produces a large amount of waste water, does not meet environmental requirement.
JACS, 73,3684 (1951) descriptions, will be 4,4-, bis- fluoro- 3- oxy butyrates ethyl esters anti-with triethyl orthoformate and acetic anhydride
(2- ethoxymeyhylenes) -4,4- difluoromethyl ethyl acetoacetates should be prepared, then 3- difluoro first are obtained with hydrazine derivate reaction
Base -1- methyl isophthalic acid H- pyrazoles -4- carboxylic acid, ethyl esters, then Jing hydrolysis obtain.But bis- fluoro- 3- oxy butyrates ethyl ester price of 4,4- used
Expensive and yield is less than 70%.
As above existing process has that being difficult to process using toxic starting materials, waste causes pollution.
The content of the invention
For the above-mentioned problems in the prior art, the technical problem to be solved is to provide a kind of for making
The intermediate of standby pyrazole carboxylic acid derivant, so as to provide a kind of preparation method of the pyrazole carboxylic acid derivant of simple economy environmental protection,
It is high that the method respectively walks reaction yield, waste gas, and waste water is few and low cost, without the need for specific response equipment.
According to the present invention, above-mentioned purpose is by being implemented as follows scheme realization.
An embodiment of the invention, the invention provides a kind of lower formula (II) compound,
Wherein
R1Selected from methyl or ethyl, preferably methyl;
R4For hydrogen or methyl, preferably methyl;
N is 0-4, preferably 0 or 1;
X is F, Cl or CF3, preferably F.
An embodiment of the invention, R1For methyl, R4For methyl, it is F that n is 1, X.
An embodiment of the invention, R1For ethyl, R4For hydrogen, it is F that n is 1, X.
An embodiment of the invention, R1For methyl, R4For hydrogen, it is F that n is 1, X.
An embodiment of the invention, R1For methyl, R4For methyl, it is F that n is 0, X.
An embodiment of the invention, R1For ethyl, R4For hydrogen, it is F that n is 0, X.
An embodiment of the invention, R1For methyl, R4For hydrogen, it is F that n is 0, X.
An embodiment of the invention, in Formula II compound during n=0, formula (II) compound structure is as follows:
Now, R1Selected from methyl or ethyl, preferably methyl;R4For hydrogen or methyl, preferably methyl.
An embodiment of the invention, the invention provides the preparation method of aforementioned formula (II) compound, described
Method is comprised the following steps:
(1) in the presence of a lewis acid, the ethene derivatives by the α of formula (III)-fluorine amine with formula (IV) react, and generate
The vinamidinium salt (i.e. 1,5- diazopentadiene salt) of formula (V),
The α of formula (III)-fluorine amine is as follows:
Wherein X is defined as described above, R2And R3Independently selected from C1-C4Alkyl, preferably methyl;
The ethene derivatives of formula (IV) are as follows:
Wherein R4For hydrogen or methyl, preferably methyl, n is 0-4, preferably 0 or 1;
And wherein as n=0, the ethene derivatives of formula (IV) are as follows:
Wherein R4For hydrogen or methyl.
The 1,5- diazopentadiene salt of formula (V) is as follows:
Wherein n, R2And R3、R4It is defined as described above, Y-For anion, the anion is selected from [BF4]-、[AlCl3F]-、
[AlF4]-、[ZnCl2F]-、[SbF6]-、[SnCl4F]-、[BiCl3F]-、[GaCl3F]-[SiCl4F]-.From corresponding Louis
This acid.
And wherein as n=0,1, the 5- diazopentadiene salt of formula (V) is as follows:
R2、R3、R4And Y-It is defined as described above.
(2) 1, the 5- diazopentadienes salt and hydrazine reaction of formula (V), obtains the compound of formula (II).
Formula (II) compound of the present invention can be as the intermediate for preparing pyrazole carboxylic acid derivant, for preparing pyrazole carboxylic acid
The intermediate of derivant.The compound of the formula (II) of n=1-4 is through hydrolysis and aoxidizes, or the compound of the formula (II) of n=0
Through oxidation, the compound of formula (I) is obtained.
Wherein R1Selected from methyl or ethyl, preferably methyl;
X is F, Cl or CF3, preferably F.
An embodiment of the invention, in step (1), lewis acid is selected from BF3、AlCl3、AlF3、ZnCl2、PF5、
SbF5、SnCl4、BiCl3、GaCl3、SiCl4Compound, preferably BF3。
An embodiment of the invention, in step (1), reaction temperature can be at -20 DEG C to 60 DEG C, and preferably -10 DEG C extremely
40 DEG C, more preferably 0 DEG C -30 DEG C.As in economic cause, step (1), reaction is preferably implemented at room temperature.
An embodiment of the invention, the α used in step (1)-fluorine amine are selected from 1,1,2,2- tetra- fluoro ethyl-N,
N- dimethyl amines, tetra- fluoro ethyl-N of 1,1,2,2-, N- diethylamides, tri- fluoro- 2- (trifluoromethyl) ethyl-N of 1,1,2-, N- diformazans
Base amine, tri- fluoro- 2- (trifluoromethyl) ethyl-N of 1,1,2-, N- diethylamides, tri- fluoro- 2- Chloroethyls-N of 1,1,2-, N- diformazans
Base amine and 1,1,2- tri- fluoro- 2- Chloroethyls-N, N- diethylamides, the α-fluorine amine preferably 1,1,2,2- tetra- fluoro ethyl-N, N-
Dimethyl amine and 1,1,2,2- tetra- fluoro ethyl-N, N- diethylamides, and particularly preferred 1,1,2,2- tetra- fluoro ethyl-N, N- diformazans
Base amine.
Lewis acidic usage amount need not be particularly limited to, an embodiment of the invention, Louis in step (1)
Acid and the mol ratio of α-fluorine amine are 1:1 to 10:Between 1, preferably 1:1 to 5:1, more preferably 1:1 to 1.3:Between 1.
The ratio of an embodiment of the invention, α-fluorine amine and ethene derivatives is 1:10 to 10:It is between 1, excellent
Select 1:5 to 5:Between 1, more preferably 1.3:1 to 1:1.3 between.
An embodiment of the invention, aforementioned method steps (2) are reacted in the presence of the solvent.Suitably
Solvent is selected from aliphatic and aromatic hydrocarbon, such as normal hexane, hexamethylene, benzene or toluene.Replaced by fluorine and chlorine atom
Aliphatic and aromatic hydrocarbon, such as dichloromethane, dichloromethane, chloroform, carbon tetrachloride, fluorobenzene, chlorobenzene
Or dichlorobenzene.Ether be it is also possible to use as solvent, suitable ether such as diethyl ether, diphenyl ether, methyl tertiary butyl ether(MTBE), isopropyl second
Base ether, dioxane, diethylene glycol dimethyl ether, diformazan ethyl glycol or THF.Nitrile be it is also possible to use as solvent, suitable nitrile such as first
Base nitrile, butyronitrile or cyanophenyl.The solvent is preferably selected from ether, acetonitrile, dichloromethane and tetrahydrofuran, particularly preferred acetonitrile or four
Hydrogen furan.
An embodiment of the invention, the hydrazine used in step (2) are methyl hydrazine or ethyl hydrazine, preferably methyl
Hydrazine.
An embodiment of the invention, 1, the 5- diazopentadienes salt of formula V and aforementioned hydrazine in step (2)
Mol ratio is 1:10 to 10:Between 1, preferably 1:5 to 5:Between 1, more preferably 1.3:1 to 1:1.3 between.
An embodiment of the invention, in step (2), reaction temperature can be at -20 DEG C to 60 DEG C, and preferably -10 DEG C extremely
40 DEG C, more preferably 0 DEG C -30 DEG C.As in economic cause, step (2), reaction is preferably implemented at room temperature.
An embodiment of the invention, is included the compound of aforementioned formula (II) in addition through hydrolysis and/or oxygen
Change, obtain the compound of formula (I).
An embodiment of the invention, the hydrolysis of formula (II) compound are carried out in the presence of the solvent, water
Mixed liquor of the solvent selected from methanol, ethanol, acetonitrile, tetrahydrofuran etc. that solution reaction is used with water, or using single water as
Solvent, preferably uses water as solvent.
An embodiment of the invention, hydrolysis can be carried out under conditions of alkalescence or acidity.Preferred acidic
Hydrolysis, acid used can be organic acid or mineral acid, preferably mineral acid.Mineral acid can for hydrochloric acid, sulphuric acid, hydrobromic acid, phosphoric acid etc.,
It is preferred that hydrochloric acid or sulphuric acid.
An embodiment of the invention, hydrolysising reacting temperature can at 30 DEG C to 100 DEG C, preferably 30 DEG C to 70 DEG C,
More preferably 50 DEG C -60 DEG C.
When being hydrolyzed in the presence of acid, formula (II) compound with acid mol ratio can be excessive acid, such as formula (II)
The mol ratio of compound and acid is 1:2 to 1:Between 10, preferably 1:3 to 1:Between 5, more preferably 1:2 to 1:Between 3.
An embodiment of the invention, the oxidant used in oxidation reaction can be hydrogen peroxide, sodium hypochlorite, height
Potassium manganate, sodium chlorate, potassium chlorate etc., preferably hydrogen peroxide or sodium hypochlorite.In oxidation reaction, oxidant is excessively used.
An embodiment of the invention, oxidation reaction are carried out in hydrolysis identical solvent, the solvent
Selected from the mixed liquor of methanol, ethanol, acetonitrile, tetrahydrofuran etc. and water, or single water as solvent, preferably water as solvent.
An embodiment of the invention, hydrolysis and oxidation reaction are carried out continuously, based on every mole of formula (II)
The amount of compound, the consumption of oxidant is 1:2 to 1:10 moles, preferably 1:3 to 1:5 moles, more preferably 1:2 to 1:3 moles.Oxygen
Change in reaction, reaction temperature can be at 30 DEG C to 100 DEG C, preferably 50 DEG C to 100 DEG C, more preferably 70 DEG C to 100 DEG C.
Description of the drawings
Fig. 1:3- (difluoromethyl) -1- methyl -4- (2- methyl-1,3-dioxy butane -2- bases) -1H- pyrazoles1H NMR
Analysis collection of illustrative plates.
Fig. 2:3- difluoromethyl -1- methyl isophthalic acid H- pyrazoles -4- formic acid1H NMR analyze collection of illustrative plates.
Fig. 3:3- (difluoromethyl) -1- methyl -4- (1,3- dioxy butane -2- bases) -1H- pyrazoles1H NMR analysis charts
Spectrum.
Fig. 4:3- (difluoromethyl) -1- methyl -4- (1,3- dioxolane -2- bases) -1H- pyrazoles1H NMR analysis charts
Spectrum.
Fig. 5:3- (difluoromethyl) -1- methyl -4- (2- methyl-1,3-dioxy pentane -2- bases) -1H- pyrazoles1H NMR
Analysis collection of illustrative plates.
Fig. 6:3- (difluoromethyl) -1- ethyl -4- (2- methyl-1,3-dioxy pentane -2- bases) -1H- pyrazoles1H NMR
Analysis collection of illustrative plates.
Fig. 7:3- difluoromethyl -1- ethyl -1H- pyrazoles -4- formic acid1H NMR analyze collection of illustrative plates.
Fig. 8:3- (difluoromethyl) -1- ethyl -4- (1,3- dioxolane -2- bases) -1H- pyrazoles1H NMR analysis charts
Spectrum.
Fig. 9:3- (difluoromethyl) -1- methyl isophthalic acid H- pyrazoles -4- ethyl ketones1H NMR analyze collection of illustrative plates.
Figure 10:3- (difluoromethyl) -1- methyl isophthalic acid H- pyrazoles -4- acetaldehyde1H NMR analyze collection of illustrative plates.
Figure 11:3- (difluoromethyl) -1- ethyl -1H- pyrazoles -4- ethyl ketones1H NMR analyze collection of illustrative plates.
Figure 12:3- (difluoromethyl) -1- methyl isophthalic acid H- pyrazoles -4- acetaldehyde1H NMR analyze collection of illustrative plates.
Figure 13:3- (difluoromethyl) -1- methyl -4- (2- methyl-1,3-dioxy hexane -2- bases) -1H- pyrazoles1H NMR
Analysis collection of illustrative plates.
Figure 14:3- (difluoromethyl) -1- methyl -4- (1,3- dioxane -2- bases) -1H- pyrazoles1H NMR analysis charts
Spectrum.
Figure 15:3- (difluoromethyl) -1- ethyl -4- (2- methyl-1,3-dioxy hexane -2- bases) -1H- pyrazoles1H NMR
Analysis collection of illustrative plates.
Figure 16:3- (difluoromethyl) -1- methyl -4- (2- methyl-1,3-dioxy heptane -2- bases) -1H- pyrazoles1H NMR
Analysis collection of illustrative plates.
Figure 17:The 1H NMR analysis charts of 3- (difluoromethyl) -1- methyl -4- (1,3- dioxy heptane -2- bases) -1H- pyrazoles
Spectrum.
Figure 18:3- (difluoromethyl) -1- ethyl -4- (2- methyl-1,3-dioxy heptane -2- bases) -1H- pyrazoles1H NMR
Analysis collection of illustrative plates.
Specific embodiment
In order that the objects, technical solutions and advantages of the present invention become more apparent, present invention specific examples below
Illustrate, described below is used only for explaining the present invention, therefore can not be interpreted as the restriction to the scope of the claims of the present invention.
It should be pointed out that all any modification, equivalent and improvement made within the spirit and principles in the present invention
Deng should be included within the scope of the present invention.
Embodiment 1:The synthesis of 3- difluoromethyl -1- methyl isophthalic acid H- pyrazoles -4- formic acid
Tetra- fluoro ethyl dimethyl of N-1,1,2,2- is put into being provided with the 1000ml four-hole bottles of agitating device and thermometer
Amine 70g (0.48mol) and acetonitrile 300g, then in 20 DEG C of Deca BF3Acetonitrile solution 150g (wherein relative to the N-1,1 for using,
2,2- tetrafluoroethyl dimethyl amines, the BF containing 1.2 equivalents3), time for adding is 15-30min, stirs 30min.Deca N, N-
Dimethyl -2- (2- methyl isophthalic acids, 3- dioxy butane -2- bases)-ethylene 81.8g (0.58mol), 30min completion of dropping.Protect at 20 DEG C
Temperature reaction 2 hours.Insulation is cooled to 5 DEG C or so after terminating, and the acetonitrile solution of Deca methyl hydrazine is (wherein relative to 1,5- diazas
Pentadiene salt, the hydrazine containing 1.1 equivalents), 30min or so completion of dropping.20 DEG C are slowly ramped to, insulation reaction 2 hours.Gained
Acetonitrile is reclaimed in vacuum distillation below 60 DEG C of reactant liquor.Add 50-60 DEG C of hot water 250g.Slowly stir, be cooled to 0 DEG C, separate out knot
Crystalline substance, crystallize time are 1-2 hours.Sucking filtration, washing, drains.It is dried, obtains product 75g, purity HPLC 99.3%, yield
93.3% (molar yield is calculated with N-1,1,2,2- tetrafluoroethyl dimethyl amines).Products therefrom is carried out1H NMR analyses, element
Analysis and mass spectral analyses, it may be determined that products obtained therefrom be 3- (difluoromethyl) -1- methyl -4- (2- methyl isophthalic acids, 3- dioxy butane -
2- yls) -1H- pyrazoles.
And the elementary analysiss of product and mass spectrometry results are as follows:
Mass spectral analyses:m/z:204.07 (100.0%), 205.07 (9.4%).
Elementary analysiss:C,47.06;H,4.94;F,18.61;N,13.72;O,15.67.
Aforesaid compound (II) 75g, water 300g are put into being provided with the 2000ml four-hole bottles of agitating device and thermometer,
30% hydrochloric acid 100g (0.82mol), is warming up to 50-60 DEG C of hydrolysis 5h, 10% liquor natrii hypochloritises 480g of Deca
(0.65mol) 100 DEG C, are warming up to, back flow reaction 5h is slowly cooled to 10 DEG C, crystallize 2h, sucking filtration, wash, drain.It is dried, obtains
To product 57.70g, 99.5% yield 91.3% (calculating molar yield with compound II) of purity HPLC.Products therefrom is carried out1H
NMR analyses, elementary analysiss and mass spectral analyses, it may be determined that products obtained therefrom is 3- difluoromethyl -1- methyl isophthalic acid H- pyrazoles -4- first
Acid.
The elementary analysiss of final product and mass spectrometry results are as follows:
Mass spectral analyses:m/z:176.04 (100.0%), 177.04 (7.3%).
Elementary analysiss:C,40.92;H,3.43;F,21.57;N,15.91;O,18.17.
Embodiment 2:The synthesis of 3- difluoromethyl -1- methyl isophthalic acid H- pyrazoles -4- formic acid
Tetra- fluoro ethyl dimethyl of N-1,1,2,2- is put into being provided with the 1000ml four-hole bottles of agitating device and thermometer
Amine 73g (0.50mol), acetonitrile 300g.Deca BF at 0 DEG C3Acetonitrile solution 180g is (wherein relative to the N-1,1,2,2- tetra- for using
Fluoro ethyl dimethyl amine, the BF containing 1.3 equivalents3), time for adding is 15-30min.Stirring at normal temperature 30min.Deca N, N- bis-
Methyl -2- (2- methyl isophthalic acids, 3- dioxy butane -2- bases)-ethylene 78g (0.55mol), 30min completion of dropping.It is incubated at 30 DEG C anti-
Answer 2 hours.Insulation is cooled to 5 DEG C or so after terminating.The acetonitrile solution of Deca methyl hydrazine is (wherein relative to 1,5- diazas penta 2
Alkene salt, the hydrazine containing 1.1 equivalents), 30min or so completion of dropping.30 DEG C are slowly ramped to, insulation reaction 2 hours.Gained reaction
Acetonitrile is reclaimed in vacuum distillation below 60 DEG C of liquid.Add 50-60 DEG C of hot water 250g.Slowly stir, be cooled to 0 DEG C, separate out crystallization, analysis
The brilliant time is 1-2 hours.Sucking filtration, washing, drains.It is dried, obtains product 74.3g, 99.1% yield 91.6% of purity HPLC
(molar yield is calculated with N-1,1,2,2- tetrafluoroethyl dimethyl amines).Products therefrom is carried out1H NMR analysis, elementary analysiss and
Mass spectral analyses, it may be determined that products obtained therefrom be 3- (difluoromethyl) -1- methyl -4- (2- methyl isophthalic acids, 3- dioxy butane -2- bases) -
1H- pyrazoles.
And the element of 3- (difluoromethyl) -1- methyl -4- (2- methyl-1,3-dioxy butane -2- bases) -1H- pyrazoles point
Analysis and mass spectrometry results are as follows:Mass spectrum:m/z:204.07 (100.0%), 205.07 (9.4%).
Elementary analysiss:C,47.06;H,4.94;F,18.61;N,13.72;O,15.67.
3- (difluoromethyl) -1- methyl -4- (2- are put into being provided with the 1000ml four-hole bottles of agitating device and thermometer
Methyl isophthalic acid, 3- dioxy butane -2- bases) -1H- pyrazoles 74.3g, water 300g, 30% hydrochloric acid 90g (0.74mol), it is warming up to 50-60
DEG C, hydrolysis 5h, 30% hydrogen peroxide 80g (0.70mol) of Deca are warming up to 100 DEG C, and back flow reaction 5h is slowly cooled to 10
DEG C, crystallize 2h, sucking filtration, washing are drained.It is dried, obtains product 60g, 99.5% yield 95.2% of purity HPLC is (with compound
II calculates molar yield).Products therefrom is carried out1H NMR analyses, elementary analysiss and mass spectral analyses, it may be determined that products obtained therefrom is
3- difluoromethyl -1- methyl isophthalic acid H- pyrazoles -4- formic acid.
Embodiment 3:The synthesis of 3- difluoromethyl -1- methyl isophthalic acid H- pyrazoles -4- formic acid
Except the N using 0.58mol, during N- dimethyl -2- (1,3- dioxy butane -2- bases)-ethylene replaces embodiment 1
Beyond N, N- dimethyl -2- (2- methyl isophthalic acids, 3- dioxy butane -2- bases)-ethylene, in repeating embodiment 1,3- (difluoro first is prepared
Base) -1- methyl -4- (2- methyl isophthalic acids, 3- dioxy butane -2- bases) -1H- pyrazoles process, and with N-1,1,2,2- tetrafluoro second
Base dimethyl amine calculates molar yield, and yield is 90.0%.Products therefrom is carried out1H NMR analyses, elementary analysiss and mass spectrum point
Analysis, it may be determined that products obtained therefrom is 3- (difluoromethyl) -1- methyl -4- (1,3- dioxy butane -2- bases) -1H- pyrazoles.
And the elementary analysiss of product and mass spectrometry results are as follows:
Mass spectral analyses:m/z:190.06 (100.0%), 191.06 (7.7%).
Elementary analysiss:C,44.22;H,4.24;F,19.98;N,14.73;O,16.83.
With 3- (difluoromethyl) -1- methyl -4- (1,3- dioxy butane -2- bases) -1H- pyrazoles for intermediate, repeat to implement
The process of 3- difluoromethyl -1- methyl isophthalic acid H- pyrazoles -4- formic acid is prepared in example 1, with 3- (difluoromethyl) -1- methyl -4- (1,3-
Dioxy butane -2- bases) on the basis of -1H- pyrazoles, molar yield is calculated, yield is 91.0%.Products therefrom is carried out1H NMR point
Analysis, elementary analysiss and mass spectral analyses, it may be determined that products obtained therefrom is 3- difluoromethyl -1- methyl isophthalic acid H- pyrazoles -4- formic acid.
Embodiment 4:The synthesis of 3- difluoromethyl -1- methyl isophthalic acid H- pyrazoles -4- formic acid
Except the N using 0.58mol, during N- dimethyl -2- (1,3- dioxolane -2- bases)-ethylene replaces embodiment 1
Beyond N, N- dimethyl -2- (2- methyl isophthalic acids, 3- dioxy butane -2- bases)-ethylene, in repeating embodiment 1,3- (difluoro first is prepared
Base) -1- methyl -4- (2- methyl isophthalic acids, 3- dioxy butane -2- bases) -1H- pyrazoles process, and with N-1,1,2,2- tetrafluoro second
Base dimethyl amine calculates molar yield, and yield is 90.4%.Products therefrom is carried out1H NMR analyses, elementary analysiss and mass spectrum point
Analysis, it may be determined that products obtained therefrom is 3- (difluoromethyl) -1- methyl -4- (1,3- dioxolane -2- bases) -1H- pyrazoles.
And the elementary analysiss of product and mass spectrometry results are as follows:
Mass spectral analyses:m/z:204.07 (100.0%), 205.07 (9.4%).
Elementary analysiss:C,47.06;H,4.94;F,18.61;N,13.72;O,15.67.
With 3- (difluoromethyl) -1- methyl -4- (1,3- dioxolane -2- bases) -1H- pyrazoles for intermediate, repeat to implement
The process of 3- difluoromethyl -1- methyl isophthalic acid H- pyrazoles -4- formic acid is prepared in example 1, with 3- (difluoromethyl) -1- methyl -4- (1,3-
Dioxolane -2- bases) on the basis of -1H- pyrazoles, molar yield is calculated, yield is 91.4%.Products therefrom is carried out1H NMR point
Analysis, elementary analysiss and mass spectral analyses, it may be determined that products obtained therefrom is 3- difluoromethyl -1- methyl isophthalic acid H- pyrazoles -4- formic acid.
Embodiment 5:The synthesis of 3- difluoromethyl -1- methyl isophthalic acid H- pyrazoles -4- formic acid
Tetra- fluoro ethyl dimethyl of N-1,1,2,2- is put into being provided with the 2000ml four-hole bottles of agitating device and thermometer
Amine 150g (1.03mol), tetrahydrofuran 800g.Then Deca BF at 0 DEG C3Tetrahydrofuran solution 350g is (wherein relative to making
N-1,1,2,2- tetrafluoroethyl dimethyl amine, the BF containing 1.3 equivalents3), time for adding is 15-30min.Stirring at normal temperature
30min.Deca N again, N- dimethyl -2- (1,3- dioxolane -2- bases)-ethylene 175g (1.13mol), 30min completion of dropping.
Insulation reaction 2 hours at 0 DEG C.Insulation is warming up to 5 DEG C or so after terminating, and the tetrahydrofuran solution of Deca methyl hydrazine is (wherein relative
In 1,5- diazopentadiene salt, the hydrazine containing 1.3 equivalents), 30min or so completion of dropping.20 DEG C are slowly ramped to, insulation is anti-
Answer 2 hours.Tetrahydrofuran is reclaimed in vacuum distillation below 60 DEG C of reactant liquor of gained.Tetrahydrofuran is evaporated as far as possible.50-60 DEG C of addition is hot
Water 500g.Slowly stir, be cooled to 0 DEG C, separate out crystallization.0 DEG C or so crystallize 1-2 hour.Sucking filtration, washing, drains.It is dried, obtains
To product 150g, (with N-1,1,2,2- tetrafluoroethyl dimethyl amine calculates mole receipts to 99.5% yield 91.6% of purity HPLC
Rate).Products therefrom is carried out1H NMR analyses, elementary analysiss and mass spectral analyses, it may be determined that products obtained therefrom be 3- (difluoromethyl)-
1- methyl -4- (1,3- dioxolane -2- bases) -1H- pyrazoles.
Stirring, thermometer are installed in 2000ml four-hole bottles.Input compound 3- (difluoromethyl) -1- methyl -4- (1,3-
Dioxolane -2- bases) -1H- pyrazoles 150g, water 600g, 30% hydrochloric acid 150g (1.23mol), 50-60 DEG C is warming up to, hydrolysis is anti-
5h, 30% hydrogen peroxide 150g (1.32mol) of Deca is answered, 100 DEG C are warming up to, back flow reaction 5h is slowly cooled to 10 DEG C, crystallize
2h, sucking filtration, washing are drained.It is dried, obtains product 120g, 99.2% yield 93.2% of purity HPLC (is calculated with compound II
Molar yield).Products therefrom is carried out1H NMR analyses, elementary analysiss and mass spectral analyses, it may be determined that products obtained therefrom is 3- difluoros
Methyl isophthalic acid-methyl isophthalic acid H- pyrazoles -4- formic acid.
Embodiment 6:The synthesis of 3- difluoromethyl -1- methyl isophthalic acid H- pyrazoles -4- formic acid
Tetra- fluoro ethyl dimethyl of N-1,1,2,2- is put into being provided with the 2000ml four-hole bottles of agitating device and thermometer
Amine 145g (1.0mol), tetrahydrofuran 700g, then Deca BF at 0 DEG C3Tetrahydrofuran solution 350g is (wherein relative to use
N-1,1,2,2- tetrafluoroethyl dimethyl amine, the BF containing 1.3 equivalents3), time for adding is 15-30min.Stirring at normal temperature
30min.Deca N again, N- dimethyl -2- (2- methyl 1,3- dioxolane -2- bases)-ethylene 185g (1.20mol), 30min drops
Add complete.Insulation reaction 2 hours at 0 DEG C.Insulation is warming up to 5 DEG C or so after terminating.The tetrahydrofuran for starting Deca methyl hydrazine is molten
Liquid (wherein relative to 1,5- diazopentadiene salt, the hydrazine containing 1.3 equivalents), 30min or so completion of dropping.It is slowly ramped to
20 DEG C, insulation reaction 2 hours.Tetrahydrofuran is reclaimed in vacuum distillation below 60 DEG C of reactant liquor of gained.Tetrahydrofuran is evaporated as far as possible.Plus
Enter 50-60 DEG C of hot water 500g.Slowly stir, be cooled to 0 DEG C, separate out crystallization.0 DEG C or so crystallize 1-2 hour.Sucking filtration, washing, takes out
It is dry.It is dried, obtains product 155g, and 99.5% yield 93.6% of purity HPLC (with N-1,1,2,2- tetrafluoroethyl dimethyl amine meter
Calculate molar yield).Products therefrom is carried out1H NMR analyses, elementary analysiss and mass spectral analyses, it may be determined that products obtained therefrom is 3- (two
Methyl fluoride) -1- methyl -4- (2- methyl-1,3-dioxy pentane -2- bases) -1H- pyrazoles.
And the elementary analysiss of product and mass spectrometry results are as follows:
Mass spectral analyses:m/z:218.09 (100.0%), 219.09 (9.9%).
Elementary analysiss:C,49.54;H,5.54;F,17.41;N,12.84;O,14.66.
3- (difluoromethyl) -1- methyl -4- (2- are put into being provided with the 3000ml four-hole bottles of agitating device and thermometer
Methyl isophthalic acid, 3- dioxolane -2- bases) -1H- pyrazoles 135g, water 500g, 30% hydrochloric acid 180g (1.32mol), it is warming up to 50-60
DEG C, hydrolysis 5h, 10% liquor natrii hypochloritises 900g (1.21mol) of Deca are warming up to 100 DEG C, and back flow reaction 5h slowly drops
To 10 DEG C, crystallize 2h, sucking filtration, washing are drained temperature.It is dried, obtains product 118g, 99.3% yield 91.8% of purity HPLC (with
Compound II calculates molar yield).Products therefrom is carried out1H NMR analyses, elementary analysiss and mass spectral analyses, it may be determined that gained
Product is 3- difluoromethyl -1- methyl isophthalic acid H- pyrazoles -4- formic acid.
Embodiment 7:The synthesis of 3- difluoromethyl -1- ethyl -1H- pyrazoles -4- formic acid
In addition to the tetrahydrofuran solution for replacing methyl hydrazine with the tetrahydrofuran solution of ethyl hydrazine, repeat embodiment 6 and make
The process of standby 3- (difluoromethyl) -1- methyl -4- (2- methyl isophthalic acids, 3- dioxolane -2- bases) -1H- pyrazoles, and with N-1,1,
2,2- tetrafluoroethyl dimethyl amines calculate molar yield, and yield is 90.9%.Products therefrom is carried out1H NMR analyses, elementary analysiss
And mass spectral analyses, it may be determined that products obtained therefrom is 3- (difluoromethyl) -1- ethyl -4- (2- methyl isophthalic acids, 3- dioxolane -2-
Base) -1H- pyrazoles (compound (II)).Structural formula is as follows:
The elementary analysiss of 3- (difluoromethyl) -1- ethyl -4- (2- methyl-1,3-dioxy pentane -2- bases) -1H- pyrazoles and
Mass spectrometry results are as follows:
Mass spectral analyses:m/z:232.10 (100.0%), 233.11 (11.1%).
Elementary analysiss:C,51.72;H,6.08;F,16.36;N,12.06;O,13.78.
With 3- (difluoromethyl) -1- ethyl -4- (2- methyl isophthalic acids, 3- dioxolane -2- bases) -1H- pyrazoles for intermediate, weight
Prepare the process of 3- difluoromethyl -1- methyl isophthalic acid H- pyrazoles -4- formic acid in multiple embodiment 6, with 3- (difluoromethyl) -1- ethyls -
On the basis of 4- (2- methyl isophthalic acids, 3- dioxolane -2- bases) -1H- pyrazoles, molar yield is calculated, yield is 91.5%.Products therefrom
Carry out1H NMR analyses, elementary analysiss and mass spectral analyses, it may be determined that products obtained therefrom is 3- difluoromethyl -1- ethyl -1H- pyrroles
Azoles -4- formic acid.The elementary analysiss of final product and mass spectrometry results are as follows:
Mass spectral analyses:m/z:190.06 (100.0%), 191.06 (7.7%).
Elementary analysiss:C,44.22;H,4.24;F,19.98;N,14.73;O,16.83.
Embodiment 8:The synthesis of 3- difluoromethyl -1- ethyl -1H- pyrazoles -4- formic acid
In addition to the tetrahydrofuran solution for replacing methyl hydrazine with the tetrahydrofuran solution of ethyl hydrazine, repeat embodiment 5 and make
The process of standby 3- (difluoromethyl) -1- methyl -4- (1,3- dioxolane -2- bases) -1H- pyrazoles, and with N-1,1,2,2- tetra-
Fluoro ethyl dimethyl amine calculates molar yield, and yield is 90.6%.Products therefrom is carried out1H NMR analyses, elementary analysiss and mass spectrum
Analysis, it may be determined that products obtained therefrom is 3- (difluoromethyl) -1- ethyl -4- (1,3- dioxolane -2- bases) -1H- pyrazoles.Structure
Formula is as follows:
The elementary analysiss of 3- (difluoromethyl) -1- ethyl -4- (1,3- dioxolane -2- bases) -1H- pyrazoles and mass spectral analyses
As a result it is as follows:
Mass spectral analyses:m/z:218.09 (100.0%), 219.09 (9.9%).
Elementary analysiss:C,49.54;H,5.54;F,17.41;N,12.84;O,14.66.
With 3- (difluoromethyl) -1- ethyl -4- (1,3- dioxolane -2- bases) -1H- pyrazoles for intermediate, repeat to implement
The process of 3- difluoromethyl -1- methyl isophthalic acid H- pyrazoles -4- formic acid is prepared in example 5, with 3- (difluoromethyl) -1- ethyls -4- (1,3-
Dioxolane -2- bases) -1H- pyrazoles benchmark, molar yield is calculated, yield is 91.2%.Products therefrom is carried out1H NMR analyses,
Elementary analysiss and mass spectral analyses, it may be determined that products obtained therefrom is 3- difluoromethyl -1- ethyl -1H- pyrazoles -4- formic acid.
Embodiment 9:The synthesis of 3- difluoromethyl -1- methyl isophthalic acid H- pyrazoles -4- formic acid
If n=0, R4=methyl, then (IV) beThat is N, N dimethylamine base propenone.
Tetra- fluoro ethyl dimethyl of N-1,1,2,2- is put into being provided with the 1000ml four-hole bottles of agitating device and thermometer
Amine 73g (0.5mol) and acetonitrile 300g, then in 20 DEG C of Deca BF3Acetonitrile solution 160g (wherein relative to the N-1,1 for using,
2,2- tetrafluoroethyl dimethyl amines, the BF containing 1.2 equivalents3), time for adding is 15-30min, stirs 30min.Deca N, N-
Dimethyl amido propenone 73.5g (0.65mol), 30min completion of dropping.Insulation reaction 2 hours at 20 DEG C.Insulation is dropped after terminating
, to 5 DEG C or so, the acetonitrile solution of Deca methyl hydrazine is (wherein relative to 1,5- diazopentadiene salt, containing 1.2 equivalents for temperature
Hydrazine), 30min or so completion of dropping.20 DEG C are slowly ramped to, insulation reaction 2 hours.Vacuum distillation below 60 DEG C of reactant liquor of gained
Reclaim acetonitrile.Add 50-60 DEG C of hot water 250g.Slowly stir, be cooled to 0 DEG C, separate out crystallization, the crystallize time is 1-2 hours.Take out
Filter, washing, drains.It is dried, obtains product 72g, purity HPLC 99.3%, yield 90.3% (with N-1,1,2,2- tetra- fluoro ethyl
Dimethyl amine calculates molar yield).Products therefrom is carried out1H NMR analyses, elementary analysiss and mass spectral analyses, it may be determined that gained
Product is 3- (difluoromethyl) -1- methyl isophthalic acid H- pyrazoles -4- ethyl ketones.
The elementary analysiss of 3- (difluoromethyl) -1- methyl isophthalic acid H- pyrazoles -4- ethyl ketones and mass spectrometry results are as follows:
Mass spectral analyses:m/z:174.06 (100.0%), 175.06 (8.3%).
Elementary analysiss:C,48.28;H,4.63;F,21.82;N,16.09;O,9.19.
Aforesaid compound (II) 72g, Deca are put into being provided with the 2000ml four-hole bottles of agitating device and thermometer
10% liquor natrii hypochloritises 500g (0.67mol), is warming up to 100 DEG C, and back flow reaction 5h is slowly cooled to 10 DEG C, and crystallize 2h takes out
Filter, washing, drains.It is dried, obtains product 56g, purity HPLC 99.5%, yield 91.3% (calculates mole receipts with compound II
Rate).Products therefrom is carried out1H NMR analyses, elementary analysiss and mass spectral analyses, it may be determined that products obtained therefrom is 3- difluoromethyl -1-
Methyl isophthalic acid H- pyrazoles -4- formic acid.
Embodiment 10:The synthesis of 3- difluoromethyl -1- methyl isophthalic acid H- pyrazoles -4- formic acid
If n=0, R4=hydrogen, then (IV) beThat is N, N dimethylamine base acrylic aldehyde
Tetra- fluoro ethyl dimethyl of N-1,1,2,2- is put into being provided with the 2000ml four-hole bottles of agitating device and thermometer
Amine 145g (1.0mol) and acetonitrile 700g, then in 20 DEG C of Deca BF3Acetonitrile solution 1650g (wherein relative to the N-1 for using,
1,2,2- tetrafluoroethyl dimethyl amine, the BF containing 1.3 equivalents3), time for adding is 15-30min, stirs 30min.Deca N,
N- dimethyl amidos acrylic aldehyde 120g (1.10mol), 30min completion of dropping.Insulation reaction 2 hours at 20 DEG C.After insulation terminates
5 DEG C or so are cooled to, the acetonitrile solution of Deca methyl hydrazine is (wherein relative to 1,5- diazopentadiene salt, containing 1 equivalent
Hydrazine), 30min or so completion of dropping.20 DEG C are slowly ramped to, insulation reaction 2 hours.Vacuum distillation below 60 DEG C of reactant liquor of gained
Reclaim acetonitrile.Add 50-60 DEG C of hot water 600g.Slowly stir, be cooled to 0 DEG C, separate out crystallization, the crystallize time is 1-2 hours.Take out
Filter, washing, drains.It is dried, obtains product 148g, purity HPLC 99.3%, yield 92.8% (with N-1,1,2,2- tetrafluoro second
Base dimethyl amine calculates molar yield).Products therefrom is carried out1H NMR analyses, elementary analysiss and mass spectral analyses, it may be determined that institute
It is 3- (difluoromethyl) -1- methyl isophthalic acid H- pyrazoles -4- formaldehyde to obtain product.
The elementary analysiss of 3- (difluoromethyl) -1- methyl isophthalic acid H- pyrazoles -4- acetaldehyde and mass spectrometry results are as follows:
Mass spectral analyses:m/z:160.04 (100.0%), 161.05 (8.3%).
Elementary analysiss:C,45.01;H,3.78;F,23.73;N,17.50;O,9.99.
Aforesaid compound (II) 148g, Deca are put into being provided with the 3000ml four-hole bottles of agitating device and thermometer
10% liquor natrii hypochloritises 1000g (1.34mol), is warming up to 100 DEG C, and back flow reaction 5h is slowly cooled to 10 DEG C, crystallize 2h,
Sucking filtration, washing, drains.It is dried, obtains product 115g, 99.5% yield 91.3% of purity HPLC is (with compound II calculating mole
Yield)..Products therefrom is carried out1H NMR analyses, elementary analysiss and mass spectral analyses, it may be determined that products obtained therefrom is 3- difluoro first
Base -1- methyl isophthalic acid H- pyrazoles -4- formic acid.
Embodiment 11:The synthesis of 3- difluoromethyl -1- ethyl -1H- pyrazoles -4- formic acid
In addition to the acetonitrile solution for replacing methyl hydrazine with the acetonitrile solution of ethyl hydrazine, in repeating embodiment 9,3- (two is prepared
Methyl fluoride) -1- methyl isophthalic acid H- pyrazoles -4- ethyl ketones process, and with N-1,1,2,2- tetrafluoroethyl dimethyl amine is calculated mole
Yield, yield are 91.4%.Products therefrom is carried out1H NMR analyses, elementary analysiss and mass spectral analyses, it may be determined that products obtained therefrom
For 3- (difluoromethyl) -1- ethyl -1H- pyrazoles -4- ethyl ketones.
The elementary analysiss of 3- (difluoromethyl) -1- ethyl -1H- pyrazoles -4- ethyl ketones and mass spectrometry results are as follows:
Mass spectral analyses:m/z:188.08 (100.0%), 189.08 (8.8%).
Elementary analysiss:C,51.06;H,5.36;F,20.19;N,14.89;O,8.50.
With 3- (difluoromethyl) -1- ethyl -1H- pyrazoles -4- ethyl ketones as intermediate, in repeating embodiment 9,3- difluoros are prepared
The process of methyl isophthalic acid-methyl isophthalic acid H- pyrazoles -4- formic acid, on the basis of 3- (difluoromethyl) -1- ethyl -1H- pyrazoles -4- ethyl ketones,
Molar yield is calculated, yield is 91.5%.Products therefrom is carried out1H NMR analyses, elementary analysiss and mass spectral analyses, it may be determined that
Products obtained therefrom is 3- difluoromethyl -1- ethyl -1H- pyrazoles -4- formic acid.
Embodiment 12:The synthesis of 3- difluoromethyl -1- ethyl -1H- pyrazoles -4- formic acid
In addition to the acetonitrile solution for replacing methyl hydrazine with the acetonitrile solution of ethyl hydrazine, repeat embodiment 10 and prepare 3- (two
Methyl fluoride) -1- methyl isophthalic acid H- pyrazoles -4- acetaldehyde process, and with N-1,1,2,2- tetrafluoroethyl dimethyl amine is calculated mole
Yield, yield are 92.4%.Products therefrom is carried out1H NMR analyses, elementary analysiss and mass spectral analyses, it may be determined that products obtained therefrom
For 3- (difluoromethyl) -1- ethyl -1H- pyrazoles -4- formaldehyde.
The elementary analysiss of 3- (difluoromethyl) -1- ethyl -1H- pyrazoles -4- acetaldehyde and mass spectrometry results are as follows:
Mass spectral analyses:m/z:1674.06 (100.0%), 175.06 (8.3%).
Elementary analysiss:C,48.28;H,4.63;F,21.82;N,16.09;O,9.19.
With 3- (difluoromethyl) -1- ethyl -1H- pyrazoles -4- acetaldehyde as intermediate, in repeating embodiment 10,3- difluoros are prepared
The process of methyl isophthalic acid-methyl isophthalic acid H- pyrazoles -4- formic acid, on the basis of 3- (difluoromethyl) -1- ethyl -1H- pyrazoles -4- acetaldehyde,
Molar yield is calculated, yield is 94.1%.Products therefrom is carried out1H NMR analyses, elementary analysiss and mass spectral analyses, it may be determined that
Products obtained therefrom is 3- difluoromethyl -1- ethyl -1H- pyrazoles -4- formic acid.
Embodiment 13:The synthesis of 3- difluoromethyl -1- methyl isophthalic acid H- pyrazoles -4- formic acid
Except using N, N- dimethyl -2- (2- methyl-1,3-dioxy hexane -2- bases)-ethylene to replace N, N- dimethyl -2-
Outside (2- methyl isophthalic acids, 3- dioxy butane -2- bases)-ethylene, repeat embodiment 2 and prepare 3- (difluoromethyl) -1- methyl -4- (2-
Methyl isophthalic acid, 3- dioxy butane -2- bases) -1H- pyrazoles process, and with N-1,1,2,2- tetrafluoroethyl dimethyl amine is calculated and is rubbed
That yield, yield is 91.9%.Products therefrom is carried out1H NMR analyses, elementary analysiss and mass spectral analyses, it may be determined that gained is produced
Product are 3- (difluoromethyl) -1- methyl -4- (2- methyl-1,3-dioxy hexane -2- bases) -1H- pyrazoles (compound (II)).Structure
Formula is as follows:
The elementary analysiss of 3- (difluoromethyl) -1- methyl -4- (2- methyl-1,3-dioxy hexane -2- bases) -1H- pyrazoles and
Mass spectrometry results are as follows:
Mass spectral analyses:m/z:232.10 (100.0%), 233.11 (11.1%).
Elementary analysiss:C,51.72;H,6.08;F,16.36;N,12.06;O,13.78.
With 3- (difluoromethyl) -1- methyl -4- (2- methyl isophthalic acids, 3- dioxane -2- bases) -1H- pyrazoles for intermediate, weight
Prepare the process of 3- difluoromethyl -1- methyl isophthalic acid H- pyrazoles -4- formic acid in multiple embodiment 2, with 3- (difluoromethyl) -1- methyl -
On the basis of 4- (2- methyl isophthalic acids, 3- dioxane -2- bases) -1H- pyrazoles, molar yield is calculated, yield is 92.3%.Products therefrom
Carry out1H NMR analyses, elementary analysiss and mass spectral analyses, it may be determined that products obtained therefrom is 3- difluoromethyl -1- methyl isophthalic acid H- pyrroles
Azoles -4- formic acid.
Embodiment 14:The synthesis of 3- difluoromethyl -1- methyl isophthalic acid H- pyrazoles -4- formic acid
Except using N, N- dimethyl -2- (1,3- dioxane -2- bases)-ethylene to replace N, N- dimethyl -2- (1,3- bis-
Oxygen pentane -2- bases) outside-ethylene, repeat embodiment 5 and prepare 3- (difluoromethyl) -1- methyl -4- (1,3- dioxolane -2-
Base) -1H- pyrazoles process, and with N-1,1,2,2- tetrafluoroethyl dimethyl amine calculates molar yield, and yield is 90.9%.
Products therefrom is carried out1H NMR analyses, elementary analysiss and mass spectral analyses, it may be determined that products obtained therefrom is 3- (difluoromethyl) -1- first
Base -4- (1,3- dioxane -2- bases) -1H- pyrazoles (compound (II)).Structural formula is as follows:
The elementary analysiss of 3- (difluoromethyl) -1- methyl -4- (1,3- dioxane -2- bases) -1H- pyrazoles and mass spectral analyses
As a result it is as follows:
Mass spectral analyses:m/z:218.09 (100.0%), 219.09 (9.9%).
Elementary analysiss:C,49.54;H,5.54;F,17.41;N,12.84;O,14.66.
With 3- (difluoromethyl) -1- methyl -4- (1,3- dioxane -2- bases) -1H- pyrazoles for intermediate, repeat to implement
The process of 3- difluoromethyl -1- methyl isophthalic acid H- pyrazoles -4- formic acid, 3- (difluoromethyl) -1- methyl -4- (1,3- bis- is prepared in example 5
Oxygen hexane -2- bases) on the basis of -1H- pyrazoles, molar yield is calculated, yield is 91.6%.Products therefrom is carried out1H NMR analyses,
Elementary analysiss and mass spectral analyses, it may be determined that products obtained therefrom is 3- difluoromethyl -1- methyl isophthalic acid H- pyrazoles -4- formic acid.
Embodiment 15:The synthesis of 3- difluoromethyl -1- ethyl -1H- pyrazoles -4- formic acid
Except using N, N- dimethyl -2- (2- methyl-1,3-dioxy hexane -2- bases)-ethylene to replace N, N- dimethyl -2-
(2- methyl isophthalic acids, 3- dioxy butane -2- bases)-ethylene, and using except replacing methyl hydrazine with the tetrahydrofuran solution of ethyl hydrazine
Acetonitrile solution outside, repeat embodiment 2 prepare 3- (difluoromethyl) -1- methyl -4- (2- methyl isophthalic acids, 3- dioxy butane -2-
Base) -1H- pyrazoles process, and with N-1,1,2,2- tetrafluoroethyl dimethyl amine calculates molar yield, and yield is 91.6%.
Products therefrom is carried out1H NMR analyses, elementary analysiss and mass spectral analyses, it may be determined that products obtained therefrom is 3- (difluoromethyl) -1- second
Base -4- (2- methyl-1,3-dioxy hexane -2- bases) -1H- pyrazoles (compound (II)).Structural formula is as follows:
The elementary analysiss of 3- (difluoromethyl) -1- ethyl -4- (2- methyl-1,3-dioxy hexane -2- bases) -1H- pyrazoles and
Mass spectrometry results are as follows:
Mass spectral analyses:m/z:246.12 (100.0%), 247.12 (12.9%), 248.12 (1.1%).
Elementary analysiss:C,53.65;H,6.55;F,15.43;N,11.38;O,12.99.
With 3- (difluoromethyl) -1- ethyl -4- (2- methyl isophthalic acids, 3- dioxane -2- bases) -1H- pyrazoles for intermediate, weight
Prepare the process of 3- difluoromethyl -1- methyl isophthalic acid H- pyrazoles -4- formic acid in multiple embodiment 2, with 3- (difluoromethyl) -1- ethyls -
On the basis of 4- (2- methyl isophthalic acids, 3- dioxane -2- bases) -1H- pyrazoles, molar yield is calculated, yield is 92.2%.Products therefrom
Carry out1H NMR analyses, elementary analysiss and mass spectral analyses, it may be determined that products obtained therefrom is 3- difluoromethyl -1- ethyl -1H- pyrroles
Azoles -4- formic acid.
Embodiment 16:The synthesis of 3- difluoromethyl -1- methyl isophthalic acid H- pyrazoles -4- formic acid
Except using N, N- dimethyl -2- (2- methyl-1,3-dioxy heptane -2- bases)-ethylene to replace N, N- dimethyl -2-
Outside (2- methyl isophthalic acids, 3- dioxy butane -2- bases)-ethylene, repeat embodiment 2 and prepare 3- (difluoromethyl) -1- methyl -4- (2-
Methyl isophthalic acid, 3- dioxy butane -2- bases) -1H- pyrazoles process, and with N-1,1,2,2- tetrafluoroethyl dimethyl amine is calculated and is rubbed
That yield, yield is 91.1%.Products therefrom is carried out1H NMR analyses, elementary analysiss and mass spectral analyses, it may be determined that gained is produced
Product are 3- (difluoromethyl) -1- methyl -4- (2- methyl-1,3-dioxy heptane -2- bases) -1H- pyrazoles (compound (II)).Structure
Formula is as follows:
The elementary analysiss of 3- (difluoromethyl) -1- methyl -4- (2- methyl-1,3-dioxy heptane -2- bases) -1H- pyrazoles and
Mass spectrometry results are as follows:
Mass spectral analyses:m/z:246.12 (100.0%), 247.12 (12.9%), 248.12 (1.1%).
Elementary analysiss:C,53.65;H,6.55;F,15.43;N,11.38;O,12.99.
With 3- (difluoromethyl) -1- methyl -4- (2- methyl isophthalic acids, 3- dioxy heptane -2- bases) -1H- pyrazoles for intermediate, weight
Prepare the process of 3- difluoromethyl -1- methyl isophthalic acid H- pyrazoles -4- formic acid in multiple embodiment 2, with 3- (difluoromethyl) -1- methyl -
On the basis of 4- (2- methyl isophthalic acids, 3- dioxy heptane -2- bases) -1H- pyrazoles, molar yield is calculated, yield is 92.0%.Products therefrom
Carry out1H NMR analyses, elementary analysiss and mass spectral analyses, it may be determined that products obtained therefrom is 3- difluoromethyl -1- methyl isophthalic acid H- pyrroles
Azoles -4- formic acid.
Embodiment 17:The synthesis of 3- difluoromethyl -1- methyl isophthalic acid H- pyrazoles -4- formic acid
Except using N, N- dimethyl -2- (1,3- dioxy heptane -2- bases)-ethylene to replace N, N- dimethyl -2- (1,3- bis-
Oxygen pentane -2- bases) outside-ethylene, repeat embodiment 5 and prepare 3- (difluoromethyl) -1- methyl -4- (1,3- dioxolane -2-
Base) -1H- pyrazoles process, and with N-1,1,2,2- tetrafluoroethyl dimethyl amine calculates molar yield, and yield is 90.8%.
Products therefrom is carried out1H NMR analyses, elementary analysiss and mass spectral analyses, it may be determined that products obtained therefrom is 3- (difluoromethyl) -1- first
Base -4- (1,3- dioxy heptane -2- bases) -1H- pyrazoles (compound (II)).Structural formula is as follows:
The elementary analysiss of 3- (difluoromethyl) -1- methyl -4- (1,3- dioxy heptane -2- bases) -1H- pyrazoles and mass spectral analyses
As a result it is as follows:
Mass spectral analyses:m/z:232.10 (100.0%), 233.11 (11.1%).
Elementary analysiss:C,51.72;H,6.08;F,16.36;N,12.06;O,13.78.
With 3- (difluoromethyl) -1- methyl -4- (1,3- dioxy heptane -2- bases) -1H- pyrazoles for intermediate, repeat to implement
The process of 3- difluoromethyl -1- methyl isophthalic acid H- pyrazoles -4- formic acid, 3- (difluoromethyl) -1- methyl -4- (1,3- bis- is prepared in example 5
Oxygen heptane -2- bases) on the basis of -1H- pyrazoles, molar yield is calculated, yield is 91.5%.Products therefrom is carried out1H NMR analyses,
Elementary analysiss and mass spectral analyses, it may be determined that products obtained therefrom is 3- difluoromethyl -1- methyl isophthalic acid H- pyrazoles -4- formic acid.
Embodiment 18:The synthesis of 3- difluoromethyl -1- ethyl -1H- pyrazoles -4- formic acid
Except using N, N- dimethyl -2- (2- methyl-1,3-dioxy heptane -2- bases)-ethylene to replace N, N- dimethyl -2-
(2- methyl isophthalic acids, 3- dioxy butane -2- bases)-ethylene, and using except replacing methyl hydrazine with the tetrahydrofuran solution of ethyl hydrazine
Acetonitrile solution outside, repeat embodiment 2 prepare 3- (difluoromethyl) -1- methyl -4- (2- methyl isophthalic acids, 3- dioxy butane -2-
Base) -1H- pyrazoles process, and with N-1,1,2,2- tetrafluoroethyl dimethyl amine calculates molar yield, and yield is 91.7%.
Products therefrom is carried out1H NMR analyses, elementary analysiss and mass spectral analyses, it may be determined that products obtained therefrom is 3- (difluoromethyl) -1- second
Base -4- (2- methyl-1,3-dioxy heptane -2- bases) -1H- pyrazoles (compound (II)).Structural formula is as follows:
The elementary analysiss of 3- (difluoromethyl) -1- ethyl -4- (2- methyl-1,3-dioxy heptane -2- bases) -1H- pyrazoles and
Mass spectrometry results are as follows:
Mass spectral analyses:m/z:260.13 (100.0%), 261.14 (13.3%), 262.14 (1.2%).
Elementary analysiss:C,55.37;H,6.97;F,14.60;N,10.76;O,12.29.
With 3- (difluoromethyl) -1- ethyl -4- (2- methyl isophthalic acids, 3- dioxy heptane -2- bases) -1H- pyrazoles for intermediate, weight
Prepare the process of 3- difluoromethyl -1- methyl isophthalic acid H- pyrazoles -4- formic acid in multiple embodiment 2, with 3- (difluoromethyl) -1- ethyls -
On the basis of 4- (2- methyl isophthalic acids, 3- dioxy heptane -2- bases) -1H- pyrazoles, molar yield is calculated, yield is 92.1%.Products therefrom
Carry out1H NMR analyses, elementary analysiss and mass spectral analyses, it may be determined that products obtained therefrom is 3- difluoromethyl -1- ethyl -1H- pyrroles
Azoles -4- formic acid.
Claims (19)
1. a kind of formula (II) compound,
Wherein
R1Selected from methyl or ethyl;
R4For hydrogen or methyl;
N is 1-4;
X is F, Cl or CF3。
2. compound according to claim 1, wherein R1For methyl.
3. compound according to claim 1, wherein R4For methyl.
4. compound according to claim 1, wherein X are F.
5. compound according to claim 1, wherein R1For methyl, R4For methyl, it is F that n is 1, X.
6. the synthetic method of formula (II) compound as claimed in claim 1, the method comprising the steps of:
(1) in the presence of a lewis acid, the ethene derivatives by the α of formula (III)-fluorine amine with formula (IV) react, and generate formula V
Vinamidinium salt (i.e. 1,5- diazopentadiene salt),
The α of formula (III)-fluorine amine is as follows:
Wherein X is defined as described above, R2And R3Independently selected from C1-C4Alkyl;
The ethene derivatives of formula (IV) are as follows:
Wherein R4For hydrogen or methyl, n is 1-4;
The 1,5- diazopentadiene salt of formula (V) is as follows:
Wherein n, R2And R3、R4It is defined as described above, Y-For anion, the anion is selected from [BF4]-、[AlCl3F]-、
[AlF4]-、[ZnCl2F]-、[SbF6]-、[SnCl4F]-、[BiCl3F]-、[GaCl3F]-[SiCl4F]-, from corresponding Louis
This acid;
(2) 1, the 5- diazopentadienes salt and hydrazine reaction of formula (V), obtains the compound of formula (II).
7. method according to claim 6, it is characterised in that:In step (1), lewis acid is selected from BF3、AlCl3、AlF3、
ZnCl2、PF5、SbF5、SnCl4、BiCl3、GaCl3、SiCl4Compound;The mol ratio of lewis acid and α-fluorine amine is 1:1 to
10:Between 1.
8. method according to claim 7, it is characterised in that:In step (1), lewis acid is selected from BF3;Lewis acid and α-
The mol ratio of fluorine amine is 1:1 to 5:1.
9. method according to claim 8, it is characterised in that:The mol ratio of lewis acid and α-fluorine amine is 1:1 to 1.3:1
Between.
10. method according to claim 6, it is characterised in that:In step (1) and (2), reaction temperature is -20 DEG C to 60
℃。
11. methods according to claim 6, it is characterised in that:In step (1) and (2), reaction temperature is -10 DEG C to 40
℃。
12. methods according to claim 6, it is characterised in that:In step (1) and (2), reaction temperature is 0 DEG C -30 DEG C.
13. methods according to claim 6, it is characterised in that step (2) is reacted in the presence of the solvent, wherein solvent are selected
From ether, acetonitrile, dichloromethane and tetrahydrofuran.
14. methods according to claim 6, it is characterised in that step (2) is reacted in the presence of the solvent, wherein solvent are selected
From acetonitrile or tetrahydrofuran.
15. methods according to claim 6, it is characterised in that the hydrazine used in step (2) is methyl hydrazine or ethyl hydrazine.
16. methods according to claim 6, it is characterised in that the hydrazine used in step (2) is methyl hydrazine.
17. methods according to claim 6, it is characterised in that in step (2) 1, the 5- diazopentadienes salt of formula V with
The mol ratio of hydrazine is 1:10 to 10:Between 1.
18. methods according to claim 6, it is characterised in that in step (2) 1, the 5- diazopentadienes salt of formula V with
The mol ratio of hydrazine is 1:5 to 5:Between 1.
19. methods according to claim 6, it is characterised in that in step (2) 1, the 5- diazopentadienes salt of formula V with
The mol ratio of hydrazine is 1.3:1 to 1:1.3 between.
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US15/737,483 US10407413B2 (en) | 2015-06-19 | 2016-06-15 | Method for preparing pyrazolecarboxylic acid derivative, and intermediate thereof |
EP16810995.7A EP3312161B1 (en) | 2015-06-19 | 2016-06-15 | Method for preparing pyrazolecarboxylic acid derivative, and intermediate thereof |
PCT/CN2016/085814 WO2016202254A1 (en) | 2015-06-19 | 2016-06-15 | Method for preparing pyrazolecarboxylic acid derivative, and intermediate thereof |
ES16810995T ES2844530T3 (en) | 2015-06-19 | 2016-06-15 | Method for preparing a derivative of pyrazolecarboxylic acid and intermediate thereof |
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CN105541716A (en) * | 2015-03-26 | 2016-05-04 | 旭硝子株式会社 | Manufacturing method for pyrazole derivatives |
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