JPH05294933A - Halogenated pyridinecarbaldehyde derivative and its production - Google Patents
Halogenated pyridinecarbaldehyde derivative and its productionInfo
- Publication number
- JPH05294933A JPH05294933A JP4125574A JP12557492A JPH05294933A JP H05294933 A JPH05294933 A JP H05294933A JP 4125574 A JP4125574 A JP 4125574A JP 12557492 A JP12557492 A JP 12557492A JP H05294933 A JPH05294933 A JP H05294933A
- Authority
- JP
- Japan
- Prior art keywords
- halogenated
- pyridinecarbaldehyde
- formula
- chloro
- acetal
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- CSDSSGBPEUDDEE-UHFFFAOYSA-N 2-formylpyridine Chemical class O=CC1=CC=CC=N1 CSDSSGBPEUDDEE-UHFFFAOYSA-N 0.000 title claims abstract description 36
- 238000004519 manufacturing process Methods 0.000 title claims description 11
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 15
- FFNVQNRYTPFDDP-UHFFFAOYSA-N 2-cyanopyridine Chemical class N#CC1=CC=CC=N1 FFNVQNRYTPFDDP-UHFFFAOYSA-N 0.000 claims abstract description 12
- 150000001875 compounds Chemical class 0.000 claims abstract description 10
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 6
- 238000010531 catalytic reduction reaction Methods 0.000 claims description 7
- 239000003377 acid catalyst Substances 0.000 claims description 5
- 125000005843 halogen group Chemical group 0.000 claims description 5
- 239000002253 acid Substances 0.000 abstract description 9
- 238000000034 method Methods 0.000 abstract description 6
- 239000003905 agrochemical Substances 0.000 abstract description 4
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract description 3
- 229910052801 chlorine Inorganic materials 0.000 abstract description 3
- 238000007796 conventional method Methods 0.000 abstract description 3
- 229940079593 drug Drugs 0.000 abstract description 3
- 239000003814 drug Substances 0.000 abstract description 3
- 230000002140 halogenating effect Effects 0.000 abstract description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract description 2
- 229910052794 bromium Inorganic materials 0.000 abstract description 2
- 239000000460 chlorine Substances 0.000 abstract description 2
- 229910052736 halogen Inorganic materials 0.000 abstract description 2
- 150000002367 halogens Chemical group 0.000 abstract description 2
- SPEUIVXLLWOEMJ-UHFFFAOYSA-N 1,1-dimethoxyethane Chemical compound COC(C)OC SPEUIVXLLWOEMJ-UHFFFAOYSA-N 0.000 abstract 2
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 abstract 1
- 239000000126 substance Substances 0.000 description 34
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 26
- 150000001241 acetals Chemical class 0.000 description 26
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 21
- 238000006243 chemical reaction Methods 0.000 description 13
- AFWWKZCPPRPDQK-UHFFFAOYSA-N 6-chloropyridine-3-carbaldehyde Chemical compound ClC1=CC=C(C=O)C=N1 AFWWKZCPPRPDQK-UHFFFAOYSA-N 0.000 description 11
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 8
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 8
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 8
- 239000007858 starting material Substances 0.000 description 7
- ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 2,3-dimethylbutane Chemical group CC(C)C(C)C ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 0.000 description 6
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 6
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 5
- 239000007868 Raney catalyst Substances 0.000 description 5
- GNFWMEFWZWXLIN-UHFFFAOYSA-N 2-bromopyridine-3-carbaldehyde Chemical compound BrC1=NC=CC=C1C=O GNFWMEFWZWXLIN-UHFFFAOYSA-N 0.000 description 4
- RTWLIQFKXMWEJY-UHFFFAOYSA-N 2-bromopyridine-4-carbaldehyde Chemical compound BrC1=CC(C=O)=CC=N1 RTWLIQFKXMWEJY-UHFFFAOYSA-N 0.000 description 4
- UFPOSTQMFOYHJI-UHFFFAOYSA-N 2-chloropyridine-4-carbaldehyde Chemical compound ClC1=CC(C=O)=CC=N1 UFPOSTQMFOYHJI-UHFFFAOYSA-N 0.000 description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
- 239000000706 filtrate Substances 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- KHPAGGHFIDLUMB-UHFFFAOYSA-N 2-chloropyridine-3-carbaldehyde Chemical compound ClC1=NC=CC=C1C=O KHPAGGHFIDLUMB-UHFFFAOYSA-N 0.000 description 3
- PVUKGNBRJFTFNJ-UHFFFAOYSA-N 6-bromopyridine-3-carbaldehyde Chemical compound BrC1=CC=C(C=O)C=N1 PVUKGNBRJFTFNJ-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 229910000564 Raney nickel Inorganic materials 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- SWTCCCJQNPGXLQ-UHFFFAOYSA-N 1-(1-butoxyethoxy)butane Chemical group CCCCOC(C)OCCCC SWTCCCJQNPGXLQ-UHFFFAOYSA-N 0.000 description 2
- ORIQLMBUPMABDV-UHFFFAOYSA-N 6-chloropyridine-3-carbonitrile Chemical compound ClC1=CC=C(C#N)C=N1 ORIQLMBUPMABDV-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- PVNIIMVLHYAWGP-UHFFFAOYSA-N Niacin Chemical compound OC(=O)C1=CC=CN=C1 PVNIIMVLHYAWGP-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 238000005984 hydrogenation reaction Methods 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 238000003760 magnetic stirring Methods 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- MAKFMOSBBNKPMS-UHFFFAOYSA-N 2,3-dichloropyridine Chemical compound ClC1=CC=CN=C1Cl MAKFMOSBBNKPMS-UHFFFAOYSA-N 0.000 description 1
- AAGDAHNUUOOXEF-UHFFFAOYSA-N 2-chloro-3-(dimethoxymethyl)pyridine Chemical compound COC(OC)C1=CC=CN=C1Cl AAGDAHNUUOOXEF-UHFFFAOYSA-N 0.000 description 1
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 238000005903 acid hydrolysis reaction Methods 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- -1 aliphatic alcohols Chemical class 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 229960003512 nicotinic acid Drugs 0.000 description 1
- 235000001968 nicotinic acid Nutrition 0.000 description 1
- 239000011664 nicotinic acid Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000006722 reduction reaction Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- G—PHYSICS
- G10—MUSICAL INSTRUMENTS; ACOUSTICS
- G10L—SPEECH ANALYSIS TECHNIQUES OR SPEECH SYNTHESIS; SPEECH RECOGNITION; SPEECH OR VOICE PROCESSING TECHNIQUES; SPEECH OR AUDIO CODING OR DECODING
- G10L19/00—Speech or audio signals analysis-synthesis techniques for redundancy reduction, e.g. in vocoders; Coding or decoding of speech or audio signals, using source filter models or psychoacoustic analysis
- G10L2019/0001—Codebooks
- G10L2019/0011—Long term prediction filters, i.e. pitch estimation
-
- G—PHYSICS
- G10—MUSICAL INSTRUMENTS; ACOUSTICS
- G10L—SPEECH ANALYSIS TECHNIQUES OR SPEECH SYNTHESIS; SPEECH RECOGNITION; SPEECH OR VOICE PROCESSING TECHNIQUES; SPEECH OR AUDIO CODING OR DECODING
- G10L19/00—Speech or audio signals analysis-synthesis techniques for redundancy reduction, e.g. in vocoders; Coding or decoding of speech or audio signals, using source filter models or psychoacoustic analysis
- G10L2019/0001—Codebooks
- G10L2019/0013—Codebook search algorithms
Landscapes
- Pyridine Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
Description
【０００１】[0001]
【産業上の利用分野】本発明は新規なハロゲン化ピリジ
ンカルバルデヒド誘導体、その製造方法及びそれを用い
たハロゲン化ピリジンカルバルデヒドの製造方法に関す
るものである。ハロゲン化ピリジンカルバルデヒド誘導
体は医農薬中間体であるハロゲン化ピリジンカルバルデ
ヒドの出発物質として有用な化合物である。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a novel halogenated pyridinecarbaldehyde derivative, a method for producing the same, and a method for producing halogenated pyridinecarbaldehyde using the same. The halogenated pyridine carbaldehyde derivative is a compound useful as a starting material for halogenated pyridine carbaldehyde, which is an intermediate for medical and agricultural chemicals.
【０００２】[0002]
【従来技術】ハロゲン化ピリジンカルバルデヒドの製造
方法としては、特開平３−５８９７２号公報に記載され
た方法が知られている。この方法は、出発物質として、
例えば２−クロロ−５−ジクロロピリジンを使用し、こ
れを加水分解して２−クロロ−５−ピリジンカルバルデ
ヒドを得る方法である。2. Description of the Related Art As a method for producing halogenated pyridine carbaldehyde, a method described in JP-A-3-58972 is known. This method uses as a starting material:
For example, 2-chloro-5-dichloropyridine is used, and this is hydrolyzed to obtain 2-chloro-5-pyridinecarbaldehyde.
【０００３】[0003]
【発明が解決しようとする課題】しかしながらこの方法
では、出発物質の２−クロロ−５−ジクロロピリジンが
工業的に入手が容易なニコチン酸から、下記の化５に示
すように、４工程を経て合成されるものである（同公報
及び特開平２−２１２４７５公報）。However, in this method, 2-chloro-5-dichloropyridine as a starting material is converted from nicotinic acid, which is industrially easily available, through four steps as shown in Chemical formula 5 below. They are synthesized (the same publication and JP-A-2-212475).
【化５】 （式中、Ｒ1はアルキル基を示す。）このように、入手
の容易な化合物からの２−クロロ−５−ジクロロピリジ
ンの合成においては、４工程もの比較的長い工程をが必
要であるから、工程が煩雑となり、当該化合物が高価な
ものとなる。したがって、２−クロロ−５−ピリジンカ
ルバルデヒドを工業的に製造する際、２−クロロ−５−
ジクロロピリジンが出発物質として有利なものとは言い
がたい。[Chemical 5] (In the formula, R 1 represents an alkyl group.) Thus, in the synthesis of 2-chloro-5-dichloropyridine from an easily available compound, four relatively long steps are required. However, the process becomes complicated and the compound becomes expensive. Therefore, when 2-chloro-5-pyridinecarbaldehyde is industrially produced, 2-chloro-5-
It is hard to say that dichloropyridine is an advantageous starting material.
【０００４】本発明の目的は、従来技術に比べて、ハロ
ゲン化ピリジンカルバルデヒドの出発物質として優れた
ハロゲン化ピリジンカルバルデヒド誘導体を提供するこ
とにある。本発明の他の目的は、ハロゲン化ピリジンカ
ルバルデヒド誘導体の製造方法及びこの化合物を出発物
質とするハロゲン化ピリジンカルバルデヒド誘導体の製
造方法を提供することにある。An object of the present invention is to provide a halogenated pyridinecarbaldehyde derivative which is superior to the prior art as a starting material for halogenated pyridinecarbaldehyde. Another object of the present invention is to provide a method for producing a halogenated pyridinecarbaldehyde derivative and a method for producing a halogenated pyridinecarbaldehyde derivative using this compound as a starting material.
【０００５】[0005]
【課題を解決するための手段】本発明は、The present invention comprises:
【化１】 （式中、Ｘはハロゲン原子を示す。Ｒはアルキル基を示
す。）で表されるハロゲン化ピリジンカルバルデヒド誘
導体、[Chemical 1] (In the formula, X represents a halogen atom and R represents an alkyl group.), A halogenated pyridinecarbaldehyde derivative represented by the formula:
【化２】 （式中、Ｘは前記に同じ。）で表されるハロゲン化シア
ノピリジン類を、酸及び[Chemical 2] (In the formula, X is the same as above.)
【化３】 （式中、Ｒは前記に同じ。）表されるアルコールの存在
下で、接触還元することを特徴とする化１で表されるハ
ロゲン化ピリジンカルバルデヒド誘導体を製造する方
法、並びに化１で表されるハロゲン化ピリジンカルバル
デヒド誘導体を、酸触媒の存在下で、加水分解すること
を特徴とする[Chemical 3] (In the formula, R is the same as the above.) A method for producing a halogenated pyridine carbaldehyde derivative represented by Chemical formula 1, which is characterized by catalytic reduction in the presence of an alcohol represented by Chemical formula 1. Characterized in that the halogenated pyridinecarbaldehyde derivative is hydrolyzed in the presence of an acid catalyst.
【化４】 （式中、Ｘは前記に同じ。）で表されるハロゲン化ピリ
ジンカルバルデヒドの製造方法に関するものである。[Chemical 4] (In the formula, X is the same as above.) The present invention relates to a method for producing a halogenated pyridinecarbaldehyde.
【０００６】本発明は、化１で表されるハロゲン化ピリ
ジンカルバルデヒド誘導体が、下記の化６（第１工程）
及び化７（第２工程）に示すように、工業的に入手容易
なシアノピリジンからわずか２工程で合成でき、このハ
ロゲン化ピリジンカルバルデヒド誘導体を酸加水分解す
ることにより、ほぼ定量的に化４で表されるハロゲン化
ピリジンカルバルデヒドが得られることが本発明者によ
り見出され、完成されたものである。In the present invention, the halogenated pyridinecarbaldehyde derivative represented by the chemical formula 1 is represented by the following chemical formula 6 (first step)
As shown in Chemical formula 7 (second step), it can be synthesized from industrially easily available cyanopyridine in only two steps, and by subjecting this halogenated pyridinecarbaldehyde derivative to acid hydrolysis, it can be almost quantitatively modified. It was found by the present inventor that the halogenated pyridinecarbaldehyde represented by
【０００７】第１工程：First step:
【化６】 （式中、Ｘは前記に同じ。）[Chemical 6] (In the formula, X is the same as above.)
【０００８】第２工程：Second step:
【化７】 （式中、Ｘ及びＲは前記に同じ。）[Chemical 7] (In the formula, X and R are the same as above.)
【０００９】化１で表されるハロゲン化ピリジンカルバ
ルデヒド誘導体において、Ｘは塩素原子、臭素原子など
のハロゲン原子であり、またＲはメチル基、エチル基、
イソプロピル基、ブチル基などのアルキル基である。化
１で表されるハロゲン化ピリジンカルバルデヒド誘導体
の具体例としては、２−クロロ−５−ピリジンカルバル
デヒド＝ジメチル＝アセタール、２−クロロ−５−ピリ
ジンカルバルデヒド＝ジエチル＝アセタール、２−クロ
ロ−５−ピリジンカルバルデヒド＝ジイソプロピル＝ア
セタール、２−クロロ−５−ピリジンカルバルデヒド＝
ジブチル＝アセタール、２−クロロ−３−ピリジンカル
バルデヒド＝ジメチル＝アセタール、２−クロロ−３−
ピリジンカルバルデヒド＝ジエチル＝アセタール、２−
クロロ−３−ピリジンカルバルデヒド＝ジイソプロピル
＝アセタール、２−クロロ−３−ピリジンカルバルデヒ
ド＝ジブチル＝アセタール、２−クロロ−４−ピリジン
カルバルデヒド＝ジメチル＝アセタール、２−クロロ−
４−ピリジンカルバルデヒド＝ジエチル＝アセタール、
２−クロロ−４−ピリジンカルバルデヒド＝ジイソプロ
ピル＝アセタール、２−クロロ−４−ピリジンカルバル
デヒド＝ジブチル＝アセタール、２−ブロモ−５−ピリ
ジンカルバルデヒド＝ジメチル＝アセタール、２−ブロ
モ−５−ピリジンカルバルデヒド＝ジエチル＝アセター
ル、２−ブロモ−５−ピリジンカルバルデヒド＝ジイソ
プロピル＝アセタール、２−ブロモ−５−ピリジンカル
バルデヒド＝ジブチル＝アセタール、２−ブロモ−３−
ピリジンカルバルデヒド＝ジメチル＝アセタール、２−
ブロモ−３−ピリジンカルバルデヒド＝ジエチル＝アセ
タール、２−ブロモ−３−ピリジンカルバルデヒド＝ジ
イソプロピル＝アセタール、２−ブロモ−３−ピリジン
カルバルデヒド＝ジブチル＝アセタール、２−ブロモ−
４−ピリジンカルバルデヒド＝ジメチル＝アセタール、
２−ブロモ−４−ピリジンカルバルデヒド＝ジエチル＝
アセタール、２−ブロモ−４−ピリジンカルバルデヒド
＝ジイソプロピル＝アセタール、２−ブロモ−４−ピリ
ジンカルバルデヒド＝ジブチル＝アセタールなどが挙げ
られる。In the halogenated pyridinecarbaldehyde derivative represented by Chemical formula 1, X is a halogen atom such as chlorine atom and bromine atom, and R is a methyl group, an ethyl group,
An alkyl group such as an isopropyl group and a butyl group. Specific examples of the halogenated pyridinecarbaldehyde derivative represented by Chemical formula 1 include 2-chloro-5-pyridinecarbaldehyde = dimethyl = acetal, 2-chloro-5-pyridinecarbaldehyde = diethyl = acetal, 2-chloro- 5-pyridinecarbaldehyde = diisopropyl = acetal, 2-chloro-5-pyridinecarbaldehyde =
Dibutyl acetal, 2-chloro-3-pyridinecarbaldehyde dimethyl acetal, 2-chloro-3-
Pyridine carbaldehyde = diethyl = acetal, 2-
Chloro-3-pyridine carbaldehyde = diisopropyl = acetal, 2-chloro-3-pyridine carbaldehyde = dibutyl = acetal, 2-chloro-4-pyridine carbaldehyde = dimethyl = acetal, 2-chloro-
4-pyridinecarbaldehyde = diethyl = acetal,
2-chloro-4-pyridine carbaldehyde = diisopropyl = acetal, 2-chloro-4-pyridine carbaldehyde = dibutyl = acetal, 2-bromo-5-pyridine carbaldehyde = dimethyl = acetal, 2-bromo-5-pyridinecarba 2-dehyde = acetal, 2-bromo-5-pyridinecarbaldehyde = diisopropyl = acetal, 2-bromo-5-pyridinecarbaldehyde = dibutyl = acetal, 2-bromo-3-
Pyridine carbaldehyde = dimethyl = acetal, 2-
Bromo-3-pyridine carbaldehyde = diethyl = acetal, 2-bromo-3-pyridine carbaldehyde = diisopropyl = acetal, 2-bromo-3-pyridine carbaldehyde = dibutyl = acetal, 2-bromo-
4-pyridinecarbaldehyde = dimethyl = acetal,
2-Bromo-4-pyridinecarbaldehyde = diethyl =
Examples thereof include acetal, 2-bromo-4-pyridinecarbaldehyde = diisopropyl = acetal, 2-bromo-4-pyridinecarbaldehyde = dibutyl = acetal and the like.
【００１０】化１で表されるハロゲン化ピリジンカルバ
ルデヒド誘導体は、種々の方法で製造することができる
が、好ましくは、化２で表されるハロゲン化シアノピリ
ジンを酸及びアルコールの存在下で接触還元することに
より製造される。The halogenated pyridinecarbaldehyde derivative represented by the chemical formula 1 can be produced by various methods, but preferably, the halogenated cyanopyridine represented by the chemical formula 2 is contacted in the presence of an acid and an alcohol. It is produced by reduction.
【００１１】化３で表されるアルコールとして、メタノ
ール、エタノール、イソプロパノール、ブタノールなど
の脂肪族アルコールを用いることができるが、メタノー
ルを用いるのが特に好ましい。化３で表されるアルコー
ルの使用量は、化２で表されるハロゲン化シアノピリジ
ンに対して１〜５０重量倍、好ましくは５〜１０重量倍
である。化２で表されるハロゲン化シアノピリジンが化
３で表されるアルコールに難溶性の場合には、アセトニ
トリル、ジオキサン等の溶媒を添加するのが好ましい。
溶媒の使用量は、化２で表されるハロゲン化シアノピリ
ジンに対して１〜５０重量倍、好ましくは５〜１０重量
倍である。As the alcohol represented by the chemical formula 3, aliphatic alcohols such as methanol, ethanol, isopropanol and butanol can be used, but it is particularly preferable to use methanol. The amount of the alcohol represented by Chemical formula 3 used is 1 to 50 times by weight, preferably 5 to 10 times by weight that of the halogenated cyanopyridine represented by Chemical formula 2. When the halogenated cyanopyridine represented by Chemical formula 2 is sparingly soluble in the alcohol represented by Chemical formula 3, it is preferable to add a solvent such as acetonitrile or dioxane.
The amount of the solvent used is 1 to 50 times by weight, preferably 5 to 10 times by weight that of the halogenated cyanopyridine represented by Chemical formula 2.
【００１２】酸としては、硫酸、塩酸、リン酸等の鉱酸
類を用いることができるが、硫酸を用いるのが特に好ま
しい。酸の使用量は、化２で表されるハロゲン化シアノ
ピリジンに対して０．５〜３倍モル、特に好ましくは１
〜２倍モルである。酸は水溶液にて接触還元に供するの
が好ましい。酸水溶液の濃度としては、２０〜８０重量
％、好ましくは６０〜７０重量％である。As the acid, mineral acids such as sulfuric acid, hydrochloric acid and phosphoric acid can be used, but sulfuric acid is particularly preferably used. The amount of the acid used is 0.5 to 3 times mol, particularly preferably 1 mol, based on the halogenated cyanopyridine represented by Chemical formula 2.
~ 2 times the molar amount. The acid is preferably subjected to catalytic reduction in an aqueous solution. The concentration of the acid aqueous solution is 20 to 80% by weight, preferably 60 to 70% by weight.
【００１３】接触還元に用いる水素化触媒としては、種
々のものを用いることができるが、好ましくはラネー触
媒、特に好ましくはラネーニッケルである。ラネー触媒
の量は化２で表されるハロゲン化シアノピリジンに対し
て１０〜５０重量％、好ましくは２０〜４０重量％であ
る。接触還元における水素圧は常圧〜１５０ｋｇ／ｃｍ
2好ましくは１０〜４０ｋｇ／ｃｍ2 である。次に反応
温度は０〜７０℃好ましくは２０〜３０℃であり、反応
時間は反応温度、触媒量により変わるが通常１〜６時間
である。このようにして生成した化１で表されるハロゲ
ン化ピリジンカルバルデヒド誘導体の単離精製は、反応
終了液から水素化触媒をろ別し、ろ液の中和、抽出を行
った後蒸留により容易に行うことができる。Various hydrogenation catalysts can be used for the catalytic reduction, but Raney catalyst is preferable, and Raney nickel is particularly preferable. The amount of Raney catalyst is 10 to 50% by weight, preferably 20 to 40% by weight, based on the halogenated cyanopyridine represented by Chemical formula 2. Hydrogen pressure in catalytic reduction is normal pressure to 150 kg / cm
2 It is preferably 10 to 40 kg / cm 2 . Next, the reaction temperature is 0 to 70 ° C., preferably 20 to 30 ° C., and the reaction time is usually 1 to 6 hours, although it varies depending on the reaction temperature and the amount of catalyst. Isolation and purification of the halogenated pyridinecarbaldehyde derivative represented by Chemical formula 1 thus produced is easy by filtering the hydrogenation catalyst from the reaction-terminated liquid, neutralizing and extracting the filtrate, and then distilling. Can be done.
【００１４】化２で表されるハロゲン化シアノピリジン
は、ハロゲン化剤として塩素、臭素などのハロゲンを用
い、シアノピリジンをハロゲン化することにより製造さ
れる。The halogenated cyanopyridine represented by Chemical formula 2 is produced by halogenating cyanopyridine using halogen such as chlorine and bromine as a halogenating agent.
【００１５】次に、化１で表されるハロゲン化ピリジン
カルバルデヒド誘導体を酸触媒の存在下で加水分解して
化４で表されるハロゲン化ピリジンカルバルデヒドを製
造する方法について説明する。この加水分解において使
用する水の量は、化１で表されるハロゲン化ピリジンカ
ルバルデヒド誘導体に対して２−１０重量倍、好ましく
は３−５重量倍である。加水分解を阻害しない限り有機
溶媒を反応系に添加することができる。有機溶媒として
はメタノール、エタノール、イソプロパノール等のアル
コール類、ベンゼン、トルエン、キシレン、シクロヘキ
サン等の炭化水素類である。Next, a method for producing the halogenated pyridine carbaldehyde represented by Chemical formula 4 by hydrolyzing the halogenated pyridine carbaldehyde derivative represented by Chemical formula 1 in the presence of an acid catalyst will be described. The amount of water used in this hydrolysis is 2 to 10 times, preferably 3 to 5 times the weight of the halogenated pyridinecarbaldehyde derivative represented by Chemical formula 1. An organic solvent can be added to the reaction system as long as it does not inhibit hydrolysis. Examples of the organic solvent include alcohols such as methanol, ethanol and isopropanol, and hydrocarbons such as benzene, toluene, xylene and cyclohexane.
【００１６】酸触媒として、塩酸、トシル酸等を用いる
ことができるが、塩酸を用いるのが、好ましい。酸触媒
の使用量は、化１で表されるハロゲン化ピリジンカルバ
ルデヒド誘導体に対して０．５〜３倍モル、特に好まし
くは１〜２倍モルである。反応温度は０〜１００℃好ま
しくは２０〜３０℃であり、反応時間は反応温度、酸量
により変わるが通常１〜３時間である。このようにして
得られた化４で表されるハロゲン化ピリジンカルバルデ
ヒドは、通常の場合反応中に結晶化し析出するので、反
応終了後、反応液からろ別して単離精製され、常法にし
たがってさらに精製することができる。As the acid catalyst, hydrochloric acid, tosylic acid and the like can be used, but hydrochloric acid is preferably used. The amount of the acid catalyst used is 0.5 to 3 times mol, particularly preferably 1 to 2 times mol, of the halogenated pyridinecarbaldehyde derivative represented by Chemical formula 1. The reaction temperature is 0 to 100 ° C, preferably 20 to 30 ° C, and the reaction time is usually 1 to 3 hours, although it varies depending on the reaction temperature and the amount of acid. The halogenated pyridine carbaldehyde represented by Chemical formula 4 thus obtained usually crystallizes and precipitates during the reaction. Therefore, after the reaction is completed, it is isolated and purified by filtration from the reaction solution and then subjected to a conventional method. It can be further purified.
【００１７】[0017]
【実施例】以下に実施例を示しさらに詳細に本発明を説
明するが、本発明はそれらの実施例に限定されるもので
はない。 実施例１ 容量５００ミリリッターの電磁攪拌式オートクレーブに
２−クロロ−５−シアノピリジン１３．９ｇ、メタノー
ル１３８．５ｇ、７０％硫酸水溶液２１．４ｇ及びラネ
ーニッケル２．８ｇを仕込み、これに水素を導入および
加熱して５０℃、２０ｋｇ／ｃｍ2 に昇温昇圧し、つい
で当該温度該圧力を保ちながら水素の導入を続け接触還
元を６時間行った。反応終了後オ−トクレ−ブを室温ま
で冷却し、反応液から触媒をろ別した。ろ液をアンモニ
ア水溶液により中和した後メタノールを留去し残渣に
水、クロロホルムを加えて不溶物をろ別した。ろ液を分
液し抽出液を取り、抽出液から溶媒を減圧下で留去し残
渣を減圧蒸留して２−クロロ−５−ピリジンジカルバル
デヒド＝ジメチル＝アセタール１１．３ｇ（収率６０．
１％）を得た。The present invention will be described in more detail with reference to the following examples, but the present invention is not limited to these examples. Example 1 A magnetic stirring autoclave having a capacity of 500 milliliters was charged with 13.9 g of 2-chloro-5-cyanopyridine, 138.5 g of methanol, 21.4 g of 70% sulfuric acid aqueous solution and 2.8 g of Raney nickel, and hydrogen was introduced into this. Then, the temperature was raised by heating to 50 ° C. and 20 kg / cm 2 , and then hydrogen was continuously introduced while maintaining the temperature and pressure, and catalytic reduction was carried out for 6 hours. After the reaction was completed, the autoclave was cooled to room temperature, and the catalyst was filtered off from the reaction solution. The filtrate was neutralized with an aqueous ammonia solution, methanol was distilled off, water and chloroform were added to the residue, and the insoluble matter was filtered off. The filtrate was separated, the extract was taken, the solvent was distilled off from the extract under reduced pressure, the residue was distilled under reduced pressure, and 2-chloro-5-pyridinedicarbaldehyde = dimethyl = acetal 11.3 g (yield 60.
1%) was obtained.
【００１８】沸点：８６〜９０℃／１ｍｍＨｇ ＩＲ ν（ＫＢｒ、ｍａｘ、ｃｍ-1）：１１００ ＮＭＲ δ（ＴＭＳ、ＣＤＣｌ3 ）： ３．３１（ｓ，
６Ｈ）、５．４５（ｓ，１Ｈ）、７．２６〜７．４５
（ｍ，１Ｈ）、７．６７〜７．８９（ｍ，１Ｈ）、８．
４０〜８．５６（ｍ，１Ｈ） ＭＳ ｍ／ｅ ： １８７（Ｍ+）Boiling point: 86 to 90 ° C./1 mmHg IR ν (KBr, max, cm −1 ): 1100 NMR δ (TMS, CDCl 3 ): 3.31 (s,
6H), 5.45 (s, 1H), 7.26 to 7.45.
(M, 1H), 7.67 to 7.89 (m, 1H), 8.
40-8.56 (m, 1H) MS m / e: 187 (M + ).
【００１９】実施例２ メタノールをエタノールに代えた以外、実施例１と同様
にして２−クロロ−５−ピリジンカルバルデヒド＝ジエ
チル＝アセタールを得た。 沸点：９５〜１０１℃／２ｍｍＨｇ ＩＲ ν（ＫＢｒ、ｍａｘ、ｃｍ-1）：１１００ ＮＭＲ δ（ＴＭＳ、ＣＤＣｌ3）１．２５（ｔ，６
Ｈ）、３．６２（ｑ，４Ｈ）、５．５８（ｓ，１Ｈ）、
７．２２〜７．５１（ｍ，１Ｈ）、７．７１〜７．９４
（ｍ，１Ｈ）、８．４６〜８．６３（ｍ，１Ｈ） ＭＳ ｍ／ｅ ：２１５（Ｍ+）、２１７（Ｍ+2）Example 2 2-Chloro-5-pyridinecarbaldehyde = diethyl = acetal was obtained in the same manner as in Example 1 except that methanol was changed to ethanol. Boiling point: 95 to 101 ° C./2 mmHg IR ν (KBr, max, cm −1 ): 1100 NMR δ (TMS, CDCl 3 ) 1.25 (t, 6
H), 3.62 (q, 4H), 5.58 (s, 1H),
7.22 to 7.51 (m, 1H), 7.71 to 7.94
(M, 1H), 8.46 to 8.63 (m, 1H) MS m / e: 215 (M + ), 217 (M +2 )
【００２０】実施例３ 容量１リッターの電磁攪拌式オートクレーブに２−クロ
ロ−５−シアノピリジン２７．８ｇ、メタノール１３
８．５ｇ、アセトニトリル１３８．５ｇ、７０％硫酸水
溶液４２．９ｇ及びラネーニッケル１１．１ｇを仕込
み、これに水素を導入し２０ｋｇ／ｃｍ2 に昇圧し、反
応温度２０℃、当該圧力を保ちながら水素の導入を続け
接触還元を６時間行った。反応後処理は実施例１と同様
に行い２−クロロ−５−ピリジンカルバルデヒド＝ジメ
チル＝アセタール２８．８ｇ（収率７６．７％）を得
た。Example 3 27.8 g of 2-chloro-5-cyanopyridine and 13 of methanol were placed in a 1-liter capacity magnetic stirring type autoclave.
8.5 g, 138.5 g of acetonitrile, 42.9 g of 70% aqueous sulfuric acid solution and 11.1 g of Raney nickel were charged, and hydrogen was introduced into this to raise the pressure to 20 kg / cm 2 , and the reaction temperature was 20 ° C., while maintaining the pressure. The introduction was continued and catalytic reduction was carried out for 6 hours. The reaction post-treatment was carried out in the same manner as in Example 1 to obtain 28.8 g (yield: 76.7%) of 2-chloro-5-pyridinecarbaldehyde = dimethyl = acetal.
【００２１】実施例４ ２−クロロ−５−ピリジンカルバルデヒド＝ジメチル＝
アセタール１８７、６ｇと水１０１９．５ｇの混合液に
濃塩酸２０６．１ｇを１８〜２２℃、１時間で滴下し
た。反応液を２〜５℃で１時間冷却し析出した結晶をろ
過した。得られた結晶を水２０３．９ｇで２回洗浄し乾
燥し２−クロロ−５−ピリジンカルバルデヒド１０９．
０ｇ（ＧＣ純度９８．８％、収率７６．１％）を得た。
なおろ液をＧＣ分析すると２−クロロ−５−ピリジンカ
ルバルデヒド３１．０ｇ（収率２１．９％）が含まれて
いた。Example 4 2-chloro-5-pyridinecarbaldehyde = dimethyl =
Concentrated hydrochloric acid 206.1 g was added dropwise to a mixed solution of acetal 187 (6 g) and water 1019.5 g at 18 to 22 ° C. over 1 hour. The reaction solution was cooled at 2 to 5 ° C for 1 hour and the precipitated crystals were filtered. The obtained crystals were washed twice with 203.9 g of water and dried to give 2-chloro-5-pyridinecarbaldehyde 109.
0 g (GC purity 98.8%, yield 76.1%) was obtained.
The filtrate was analyzed by GC to find that it contained 31.0 g (yield 21.9%) of 2-chloro-5-pyridinecarbaldehyde.
【００２２】[0022]
【発明の効果】本発明によれば、化１で表されるハロゲ
ン化ピリジンカルバルデヒド誘導体は、医農薬中間体と
して有用な化４で表されるハロゲン化ピリジンカルバル
デヒドを製造する際の出発物質として重要であり、当該
ハロゲン化ピリジンカルバルデヒド誘導体を経由するこ
とにより、工業的規模で入手できる化合物から従来方法
に比べて少ない工程数で当該ハロゲン化ピリジンカルバ
ルデヒド製造することができる。INDUSTRIAL APPLICABILITY According to the present invention, the halogenated pyridinecarbaldehyde derivative represented by Chemical formula 1 is a starting material for producing the halogenated pyridinecarbaldehyde represented by Chemical formula 4, which is useful as an intermediate for medicines and agricultural chemicals. By passing through the halogenated pyridine carbaldehyde derivative, the halogenated pyridine carbaldehyde can be produced from a compound that is available on an industrial scale in a smaller number of steps than conventional methods.
Claims (3)
す。）で表されるハロゲン化ピリジンカルバルデヒド誘
導体。Claims: (In the formula, X represents a halogen atom and R represents an alkyl group.) A halogenated pyridinecarbaldehyde derivative represented by the formula:
ン化シアノピリジン類を、酸及び 【化３】 （式中、Ｒはアルキル基を示す。）表されるアルコール
の存在下で、接触還元することを特徴とする請求項１記
載の化合物を製造する方法。2. (In the formula, X represents a halogen atom.), And a halogenated cyanopyridine represented by the formula (In the formula, R represents an alkyl group.) Catalytic reduction is carried out in the presence of an alcohol represented by the method for producing the compound according to claim 1.
で、加水分解することを特徴とする 【化４】 （式中、Ｘはハロゲン原子を示す。）で表されるハロゲ
ン化ピリジンカルバルデヒドの製造方法。3. The compound according to claim 1 is hydrolyzed in the presence of an acid catalyst. (In the formula, X represents a halogen atom.) A method for producing a halogenated pyridinecarbaldehyde.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP04125574A JP3098099B2 (en) | 1992-04-17 | 1992-04-17 | Halogenated pyridine carbaldehyde derivative and method for producing the same |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP04125574A JP3098099B2 (en) | 1992-04-17 | 1992-04-17 | Halogenated pyridine carbaldehyde derivative and method for producing the same |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH05294933A true JPH05294933A (en) | 1993-11-09 |
| JP3098099B2 JP3098099B2 (en) | 2000-10-10 |
Family
ID=14913556
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP04125574A Expired - Fee Related JP3098099B2 (en) | 1992-04-17 | 1992-04-17 | Halogenated pyridine carbaldehyde derivative and method for producing the same |
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| Country | Link |
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Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2011162494A (en) * | 2010-02-12 | 2011-08-25 | Yuki Gosei Kogyo Co Ltd | Method for producing 4-formylpiperidine acetal derivative |
-
1992
- 1992-04-17 JP JP04125574A patent/JP3098099B2/en not_active Expired - Fee Related
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2011162494A (en) * | 2010-02-12 | 2011-08-25 | Yuki Gosei Kogyo Co Ltd | Method for producing 4-formylpiperidine acetal derivative |
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| Publication number | Publication date |
|---|---|
| JP3098099B2 (en) | 2000-10-10 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| LAPS | Cancellation because of no payment of annual fees |