US20030083350A1 - 1-(2-chloro-5-methyl-3-pyridylmethyl)-2-nitroiminiomidazolidine and process for the preparation thereof - Google Patents
1-(2-chloro-5-methyl-3-pyridylmethyl)-2-nitroiminiomidazolidine and process for the preparation thereof Download PDFInfo
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- US20030083350A1 US20030083350A1 US09/984,456 US98445601A US2003083350A1 US 20030083350 A1 US20030083350 A1 US 20030083350A1 US 98445601 A US98445601 A US 98445601A US 2003083350 A1 US2003083350 A1 US 2003083350A1
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- chloro
- methyl
- pyridylmethyl
- chloromethyl
- nitroimino
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- 238000000034 method Methods 0.000 title claims abstract description 15
- 238000002360 preparation method Methods 0.000 title claims abstract description 7
- QMGOQZVMOIWWHO-UHFFFAOYSA-N 2-chloro-3-(chloromethyl)-5-methylpyridine Chemical compound CC1=CN=C(Cl)C(CCl)=C1 QMGOQZVMOIWWHO-UHFFFAOYSA-N 0.000 claims description 13
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims description 12
- DJZWNSRUEJSEEB-UHFFFAOYSA-N n-(4,5-dihydro-1h-imidazol-2-yl)nitramide Chemical compound [O-][N+](=O)NC1=NCCN1 DJZWNSRUEJSEEB-UHFFFAOYSA-N 0.000 claims description 9
- 238000006243 chemical reaction Methods 0.000 claims description 8
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 claims description 8
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 claims description 8
- ZKCWUUTWVUVPKI-UHFFFAOYSA-N (2-chloro-5-methylpyridin-3-yl)methanol Chemical compound CC1=CN=C(Cl)C(CO)=C1 ZKCWUUTWVUVPKI-UHFFFAOYSA-N 0.000 claims description 4
- 239000003960 organic solvent Substances 0.000 claims description 4
- 229910000027 potassium carbonate Inorganic materials 0.000 claims description 4
- IZDJJYRXECMSLX-UHFFFAOYSA-N 2-chloro-5-methylpyridine-3-carbaldehyde Chemical compound CC1=CN=C(Cl)C(C=O)=C1 IZDJJYRXECMSLX-UHFFFAOYSA-N 0.000 claims description 3
- 239000012279 sodium borohydride Substances 0.000 claims description 3
- 229910000033 sodium borohydride Inorganic materials 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 abstract description 14
- -1 nitroimino pyridyl Chemical class 0.000 abstract description 7
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 12
- 239000002904 solvent Substances 0.000 description 10
- VIOXXHWSRROMRT-UHFFFAOYSA-N n-[1-[(2-chloro-5-methylpyridin-3-yl)methyl]-4,5-dihydroimidazol-2-yl]nitramide Chemical compound CC1=CN=C(Cl)C(CN2C(NCC2)=N[N+]([O-])=O)=C1 VIOXXHWSRROMRT-UHFFFAOYSA-N 0.000 description 8
- 125000003118 aryl group Chemical group 0.000 description 7
- 239000002917 insecticide Substances 0.000 description 7
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 6
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 6
- 239000000575 pesticide Substances 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 238000011097 chromatography purification Methods 0.000 description 4
- 239000010410 layer Substances 0.000 description 4
- 229940073584 methylene chloride Drugs 0.000 description 4
- 239000012044 organic layer Substances 0.000 description 4
- 239000000741 silica gel Substances 0.000 description 4
- 229910002027 silica gel Inorganic materials 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 3
- 229910052938 sodium sulfate Inorganic materials 0.000 description 3
- 235000011152 sodium sulphate Nutrition 0.000 description 3
- AIYUHDOJVYHVIT-UHFFFAOYSA-M caesium chloride Chemical compound [Cl-].[Cs+] AIYUHDOJVYHVIT-UHFFFAOYSA-M 0.000 description 2
- YWTYJOPNNQFBPC-UHFFFAOYSA-N imidacloprid Chemical compound [O-][N+](=O)\N=C1/NCCN1CC1=CC=C(Cl)N=C1 YWTYJOPNNQFBPC-UHFFFAOYSA-N 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000012257 stirred material Substances 0.000 description 2
- DKYBVKMIZODYKL-UHFFFAOYSA-N 1,3-diazinane Chemical class C1CNCNC1 DKYBVKMIZODYKL-UHFFFAOYSA-N 0.000 description 1
- DBNWKFDFDWDROA-UHFFFAOYSA-N 1-ethenylimidazolidine Chemical class C=CN1CCNC1 DBNWKFDFDWDROA-UHFFFAOYSA-N 0.000 description 1
- BGIQUVWIKRSBCR-UHFFFAOYSA-N 2-amino-4,5-dihydroimidazole-1-carbonitrile Chemical class N=C1NCCN1C#N BGIQUVWIKRSBCR-UHFFFAOYSA-N 0.000 description 1
- PGSHQANDAMACEF-UHFFFAOYSA-N 2-phenyl-1h-imidazole-4,5-dicarbonitrile Chemical class N1C(C#N)=C(C#N)N=C1C1=CC=CC=C1 PGSHQANDAMACEF-UHFFFAOYSA-N 0.000 description 1
- 241000086608 Empoasca vitis Species 0.000 description 1
- 241000258937 Hemiptera Species 0.000 description 1
- 241000238631 Hexapoda Species 0.000 description 1
- 241000358422 Nephotettix cincticeps Species 0.000 description 1
- 102000019315 Nicotinic acetylcholine receptors Human genes 0.000 description 1
- 108050006807 Nicotinic acetylcholine receptors Proteins 0.000 description 1
- 241000209094 Oryza Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- BOTHYGFNYUKJKM-UHFFFAOYSA-N [O-][N+](N=[SH]C(O)=S)=O Chemical class [O-][N+](N=[SH]C(O)=S)=O BOTHYGFNYUKJKM-UHFFFAOYSA-N 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 125000000304 alkynyl group Chemical group 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 125000000262 haloalkenyl group Chemical group 0.000 description 1
- 150000002391 heterocyclic compounds Chemical class 0.000 description 1
- 230000000749 insecticidal effect Effects 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- 125000004076 pyridyl group Chemical group 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N51/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds having the sequences of atoms O—N—S, X—O—S, N—N—S, O—N—N or O-halogen, regardless of the number of bonds each atom has and with no atom of these sequences forming part of a heterocyclic ring
Definitions
- the present invention relates to 1-(2-chloro-5-methyl-3-pyridylmethyl)-2-nitroiminoimadozolidine of the formula 1 given below and to a process for the preparation thereof.
- 1-(2-chloro-5-methyl-3-pyridylmethyl)-2-nitroiminoimadozolidine of the formula 1 is a novel compound of class nitroimino pyridyl derivatives.
- the present invention also relates to a process for the preparation of 1-(2-chloro-5-methyl-3-pyridylmethyl)-2-nitroiminoimadozolidine using 2-chloro-3-chloromethyl-5-methylpyridine and 2-nitroimino-1,3-diazacyclopentane in various solvents using a base under appropriate conditions of mole ratio, time, temperature and work up procedure with high yields and selectivity.
- 1-(2-chloro-5-pyridylmethyl) 2-nitoiminoimidazolidine is a potent insecticide (EP 0192061, 1990 and Angew.Chem.Int.Ed. 39, 1724, 2000) and acts at the nicotinic acetylcholine receptor (J.Labelled.Compd.Radiopharm, 31(8), 609, 1992; CA 117:171316w).
- N-nitroiminoimidazolidines derivatives of 2-chloropyridine-5-yl, 2-chlorothiazol-5-yl are reported as active ingredients of insecticides (JP 06122680, 1994; CA 121:p157642a & JP 06100557, 1994; CA 121:255796y).
- N-nitroiminodithiocarbonate compounds serve as intermediates for insecticides and pharmaceuticals (U.S. Pat. No.
- N-substituted alkyl, haloalkenyl, alkynyl, aralkyl, aromatic heterocyclymethyl compounds serve as insecticides (JP 02207083, 1990; CA 114:62097t).
- N-vinyl imidazolidine derivatives and 2-phenyl dicyano imidazoles are reported as insecticides and anthelminitics (EP 547557, 1993; CA119:225953p and Ger.Offen DE 19548914, 1994; CA 125:142731n).
- the main object of the invention is to provide new compounds for use as pesticides for effective crop protection.
- the present invention relates to a novel compound 1-(2-chloro-5-methyl-3-pyridylmethyl)-2-nitroiminoimadozolidine of the formula 1 given below
- the present invention also relates to a process for the preparation of 1-(2-chloro-5-methyl-3-pyridylmethyl)-2-nitroiminoimadozolidine of the formula 1
- the organic solvent used comprises acetonitrile.
- the base used comprises potassium carbonate.
- reaction is carried out for a time period in the range of 5 to 10 hours.
- the molar ratio of 2-chloro-3-chloromethyl-5-methyl pyridine to 2-nitroimino-1,3-diazacyclopentane is in the range of 1:1-1.5, preferably 1:1.2.
- 2-chloro-3-chloromethyl-5-methyl pyridine is obtained by the reaction of 2-chloro-3-hydroxymethyl-5-methyl pyridine with thionyl chloride with 90% yield.
- 2-chloro-3-chloromethyl-5-methyl pyridine is obtained by the sodium borohydride reduction of 2-chloro-5-methylpyridine-3-carbaldehyde with 88% yield.
- the compound of the invention is a novel compound and is useful as a pesticide.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyridine Compounds (AREA)
Abstract
The present invention relates to 1-(2-chloro-5-methyl-3-pyridylmethyl)-2-nitroiminoimadozolidine of the formula 1, a novel compound of class nitroimino pyridyl derivatives and to a process for the preparation thereof
Description
- The present invention relates to 1-(2-chloro-5-methyl-3-pyridylmethyl)-2-nitroiminoimadozolidine of the formula 1 given below and to a process for the preparation thereof.
- 1-(2-chloro-5-methyl-3-pyridylmethyl)-2-nitroiminoimadozolidine of the formula 1 is a novel compound of class nitroimino pyridyl derivatives. The present invention also relates to a process for the preparation of 1-(2-chloro-5-methyl-3-pyridylmethyl)-2-nitroiminoimadozolidine using 2-chloro-3-chloromethyl-5-methylpyridine and 2-nitroimino-1,3-diazacyclopentane in various solvents using a base under appropriate conditions of mole ratio, time, temperature and work up procedure with high yields and selectivity.
- 1-(6-chloronicotinyl)-2-nitroiminoimidazolidine and related compounds are reported as effectively controlling hemiptera, other sucking insects and against green rice leaf hopper [Biosci. Biotech. Biochem, 56(8), 1364 & 56(2), 364, 1992]. Structural modification in the 6-chloropyridyl and introduction of five membered hetero cyclic compounds are reported as insecticidal compounds [Biosci. Biotech. Biochem., 57(1), 127, 1993]. 1-(2-chloro-5-pyridylmethyl) 2-nitoiminoimidazolidine (Imidacloropid/Confidor) is a potent insecticide (EP 0192061, 1990 and Angew.Chem.Int.Ed. 39, 1724, 2000) and acts at the nicotinic acetylcholine receptor (J.Labelled.Compd.Radiopharm, 31(8), 609, 1992; CA 117:171316w).
- Substituted pyridinyl, pyurazinyl or pyrimidyl nitromethylene and nitroimininoimidazolidines and their synergistic mixtures are reported for moth proofing (EP 387663, 1989; CA 114:p201780 a). 2-nitroimino or cyano iminoimidazolidines and hexahydropyrimidine derivatives are reported as insecticides (JP 63156786, 1988; CA 110:p8210d). 1-diazinyl methyl-2-nitro methylene and 2-nitroiminoimidazolidines reported as new potential insecticides against green leaf hoppers on rice seedling in spray applications (Nippon Noyaku Gakkaishi 18(1), 119, 1993; CA 119:111238d). N-nitroiminoimidazolidines derivatives of 2-chloropyridine-5-yl, 2-chlorothiazol-5-yl are reported as active ingredients of insecticides (JP 06122680, 1994; CA 121:p157642a & JP 06100557, 1994; CA 121:255796y). N-nitroiminodithiocarbonate compounds serve as intermediates for insecticides and pharmaceuticals (U.S. Pat. No. 5,453,529, 1995; CA 124:p55973d). N-substituted alkyl, haloalkenyl, alkynyl, aralkyl, aromatic heterocyclymethyl compounds serve as insecticides (JP 02207083, 1990; CA 114:62097t). N-vinyl imidazolidine derivatives and 2-phenyl dicyano imidazoles are reported as insecticides and anthelminitics (EP 547557, 1993; CA119:225953p and Ger.Offen DE 19548914, 1994; CA 125:142731n).
- The discovery of new compounds for use as pesticides is still desired for effective crop protection.
- The main object of the invention is to provide new compounds for use as pesticides for effective crop protection.
- It is another object of the invention to provide new compounds for use as pesticides with good yield and selectivity.
- It is a further object of the invention to provide a new compound 1-(2-chloro-5-methyl-3-pyridylmethyl)-2-nitroiminoimadozolidine of the class of nitroimino pyridyl derivatives for use as pesticide.
- It is another object of the invention to provide a process for the preparation of a novel compound 1-(2-chloro-5-methyl-3-pyridylmethyl)-2-nitroiminoimadozolidine where the reaction time is short and the temperature conditions are mild.
- Accordingly, the present invention relates to a novel compound 1-(2-chloro-5-methyl-3-pyridylmethyl)-2-nitroiminoimadozolidine of the formula 1 given below
- The present invention also relates to a process for the preparation of 1-(2-chloro-5-methyl-3-pyridylmethyl)-2-nitroiminoimadozolidine of the formula 1
- using 2-chloro-3-chloromethyl-5-methyl pyridine and 2-nitroimino-1,3-diazacyclopentane in the presence of a base and an organic solvent.
- In one embodiment of the invention, the organic solvent used comprises acetonitrile.
- In another embodiment of the invention, the base used comprises potassium carbonate.
- In a further embodiment of the invention, the reaction is carried out for a time period in the range of 5 to 10 hours.
- In yet another embodiment of the invention, the molar ratio of 2-chloro-3-chloromethyl-5-methyl pyridine to 2-nitroimino-1,3-diazacyclopentane is in the range of 1:1-1.5, preferably 1:1.2.
- In another embodiment of the invention, 2-chloro-3-chloromethyl-5-methyl pyridine is obtained by the reaction of 2-chloro-3-hydroxymethyl-5-methyl pyridine with thionyl chloride with 90% yield.
- In another embodiment of the reaction, 2-chloro-3-chloromethyl-5-methyl pyridine is obtained by the sodium borohydride reduction of 2-chloro-5-methylpyridine-3-carbaldehyde with 88% yield.
- The invention will be described in detail with reference to the following examples, which are illustrative and should not be construed as limiting the scope of the invention in any manner.
- 2-chloro-3-chloromethyl-5-methylpyridine (1.3 g, 0.0076 moles) was added to a well-stirred material comprising of 2-nitroimino-1,3-diazacyclopentane (1.18 g, 0.00912 moles), potassium carbonate (1.16g, 0.0083 moles), cesium chloride (0.04 g, 0.00024 moles) in acetonitrile (10 ml) solvent at room temperature. The reaction mixture was refluxed for 5 hours. Solvent was removed under reduced pressure and the mass diluted with water (25 ml). The mass was then extracted with methylene chloride (2×50 ml) and the layers were separated. Organic layer was dried over sodium sulphate and solvent removed under reduced pressure. The residue obtained was subjected to chromatographic purification on silica gel to give 1-(2-chloro-5-methyl-3-pyridylmethyl) 2-nitroiminoimidazolidine in 90% yield.
- NMR (CDCl 3+DMSO d6): δ2.38 (s, 3H, CH3), 3.58 (t, 2H, N—CH2), 3.74 (t, 2H—CH2), 4.52 (s, 2H, CH2), 7.54 (s, 1H, aromatic), 8.12 (s, 1H, aromatic), 8.86 (1H, NH). Mass: M+. 269.
- 2-chloro-3-chloromethyl-5-methylpyridine (1.3 g, 0.0076 moles) was added to a well-stirred material comprising of 2-nitroimino-1,3-diazacyclopentane (1.18 g, 0.00912 moles), potassium carbonate (1.16 g, 0.0083 moles), cesium chloride (0.04 g, 0.00024 moles) in acetonitrile (20 ml) solvent at room temperature. The reaction mixture was refluxed for 8 hours. The solvent was removed under reduced pressure and the mass diluted with water (25 ml). The mass was then extracted with methylene chloride (2×50 ml) and the layers were separated. Organic layer was dried over sodium sulphate and solvent removed under reduced pressure. The residue thus obtained was subjected to chromatographic purification on silica gel to give 1-(2-chloro-5-methyl-3-pyridylmethyl) 2-nitroiminoimidazolidine in 90% yield.
- Sodium borohydride (0.65 g, 0.0167 moles) was added slowly to a well-stirred solution of 2-chloro-5-methylpyridine-3-carbaldehyde (1.3 g, 0.0084 moles) in methanol (20 ml) at 0° C. temperature over a period of 15 minutes. The reaction mass was further stirred for 2 hours at the same temperature. The solvent was removed under reduced pressure and the mass was quenched with water (25 ml). The mass was extracted with ethyl acetate (2×50 ml) and the layers separated. The organic layer was removed under reduced pressure. The residue so obtained was subjected to chromatographic purification on silica gel to give 2-chloro-3-hydroxymethyl-5-methylpyridine as a solid in 88% yield.
- NMR (CDCl 3): δ2.34 (s, 3H, CH3), 3.7 (1H, OH), 4.68 (s, 2H, CH2), 7.68 (s, 1H, aromatic), 8.04 (s, 1H, aromatic). Mass: M+. 157.
- Thionyl chloride (2.73 g, 0.023 moles) was added slowly to a well-stirred solution of 2-chloro-3-hydroxymethyl-5-methylpyridine (1.2 g, 0.0076 moles) in methylenechloride (20 ml) at 0° C. temperature over a period of 20 minutes. The reaction mass was further stirred for 6 hours at the same temperature. The solvent and excess thionylchloride was removed under reduced pressure and the mass was quenched with water (25 ml). The mass was extracted with methylene chloride (2×50 ml) and the layers separated. The organic layer was dried over sodium sulphate and the solvent removed under reduced pressure. The residue so obtained was subjected to chromatographic purification on silica gel to give 2-chloro-3-chloromethyl-5-methylpyridine as a solid in 92% yield.
- NMR (CDCl 3): δ2.36 (s, 3H, CH3), 4.6 (s, 2H, CH2), 7.62 (s, 1H, aromatic), 8.16 (s, 1H, aromatic). Mass: M+. 175.
- Advantages of the Invention
- 1. The compound of the invention is a novel compound and is useful as a pesticide.
- 2. The yield of the compound is high
- 3. The reaction is carried out at low temperature and short reaction times making the process cost effective
- 4. Isolation of the product is simple.
Claims (9)
1. 1-(2-chloro-5-methyl-3-pyridylmethyl)-2-nitroiminoimadozolidine of the general formula 1
2. A process for the preparation of 1-(2-chloro-5-methyl-3-pyridylmethyl)-2-nitroiminoimadozolidine of the formula 1
comprising reacting 2-chloro-3-chloromethyl-5-methyl pyridine and 2-nitroimino-1,3-diazacyclopentane in the presence of a base and an organic solvent.
3. A process as claimed in claim 2 wherein said base used comprises potassium carbonate.
4. A process as claimed in claim 2 wherein the organic solvent used comprises acetonitrile.
5. A process as claimed in claim 2 wherein the reaction is carried out for a time period in the range of 5 to 10 hours.
6. A process as claimed in claim 2 wherein the molar ratio of 2-chloro-3-chloromethyl-5-methyl pyridine to 2-nitroimino-1,3-diazacyclopentane is in the range of 1:1-1.5.
7. A process as claimed in claim 6 wherein the molar ratio of 2-chloro-3-chloromethyl-5-methyl pyridine to 2-nitroimino-1,3-diazacyclopentane is 1:1.2.
8. A process as claimed in claim 2 wherein 2-chloro-3-chloromethyl-5-methyl pyridine used is obtained by sodium borohydride reduction of 2-chloro-5-methylpyridine-3-carbaldehyde.
9. A process as claimed in claim 2 wherein the 2-chloro-3-chloromethyl-5-methyl pyridine used is obtained by the reaction of 2-chloro-3-hydroxymethyl-5-methyl pyridine with thionyl chloride.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP01309133A EP1306374A1 (en) | 2001-10-29 | 2001-10-29 | 1-(2-chloro-5-methyl-3-pyridylmethyl)-2-nitroiminoimadozolidine and a process for the preparation thereof |
| US09/984,456 US6566528B1 (en) | 2001-10-29 | 2001-10-30 | 1-(2-chloro-5-methyl-3-pyridylmethyl)-2-nitroiminoimidazolidine and process for the preparation thereof |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP01309133A EP1306374A1 (en) | 2001-10-29 | 2001-10-29 | 1-(2-chloro-5-methyl-3-pyridylmethyl)-2-nitroiminoimadozolidine and a process for the preparation thereof |
| US09/984,456 US6566528B1 (en) | 2001-10-29 | 2001-10-30 | 1-(2-chloro-5-methyl-3-pyridylmethyl)-2-nitroiminoimidazolidine and process for the preparation thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| US20030083350A1 true US20030083350A1 (en) | 2003-05-01 |
| US6566528B1 US6566528B1 (en) | 2003-05-20 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US09/984,456 Expired - Fee Related US6566528B1 (en) | 2001-10-29 | 2001-10-30 | 1-(2-chloro-5-methyl-3-pyridylmethyl)-2-nitroiminoimidazolidine and process for the preparation thereof |
Country Status (2)
| Country | Link |
|---|---|
| US (1) | US6566528B1 (en) |
| EP (1) | EP1306374A1 (en) |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0192060B1 (en) * | 1985-02-04 | 1991-09-18 | Nihon Bayer Agrochem K.K. | Heterocyclic compounds |
| JPH072736B2 (en) * | 1985-08-27 | 1995-01-18 | 日本バイエルアグロケム株式会社 | Nitromethylene derivative, its manufacturing method and insecticide |
| JPH0717621B2 (en) * | 1986-03-07 | 1995-03-01 | 日本バイエルアグロケム株式会社 | New heterocyclic compound |
| US5521176A (en) * | 1989-11-28 | 1996-05-28 | Nihon Bayer Agrochem K.K. | Agrochemical compositions containing certain N-heterocycligs, compounds and stabilizer |
| JP2852947B2 (en) * | 1989-11-28 | 1999-02-03 | 日本バイエルアグロケム株式会社 | Stabilized pesticide composition |
| IL99445A (en) * | 1990-09-18 | 1996-06-18 | Ciba Geigy Ag | Picoline oxides process for their preparation and insecticidal and acaricidal compositions containing them |
| DE69418641T2 (en) * | 1993-04-01 | 1999-10-07 | Shell Internationale Research Maatschappij B.V., Den Haag/S'gravenhage | Molluscicides |
| US6307053B1 (en) * | 2000-12-29 | 2001-10-23 | Sinon Corporation | Process for preparing imidacloprid |
-
2001
- 2001-10-29 EP EP01309133A patent/EP1306374A1/en not_active Ceased
- 2001-10-30 US US09/984,456 patent/US6566528B1/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| US6566528B1 (en) | 2003-05-20 |
| EP1306374A1 (en) | 2003-05-02 |
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