TW337984B - Processes for preparing indeno{1,2-e}{1,3,4}oxadiazine-dicarboxylates - Google Patents
Processes for preparing indeno{1,2-e}{1,3,4}oxadiazine-dicarboxylates Download PDFInfo
- Publication number
- TW337984B TW337984B TW86108354A TW86108354A TW337984B TW 337984 B TW337984 B TW 337984B TW 86108354 A TW86108354 A TW 86108354A TW 86108354 A TW86108354 A TW 86108354A TW 337984 B TW337984 B TW 337984B
- Authority
- TW
- Taiwan
- Prior art keywords
- formula
- compound
- acid
- methane
- ministry
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 30
- JPWPEVOWBFNRBR-UHFFFAOYSA-N indeno[1,2-e][1,3,4]oxadiazine-3,5-dicarboxylic acid Chemical class N1=C(C(O)=O)OC2=C(C(=O)O)C3=CC=CC=C3C2=N1 JPWPEVOWBFNRBR-UHFFFAOYSA-N 0.000 title 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 58
- 150000001875 compounds Chemical class 0.000 claims description 42
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 37
- 238000006243 chemical reaction Methods 0.000 claims description 27
- 125000003545 alkoxy group Chemical group 0.000 claims description 22
- 239000002253 acid Substances 0.000 claims description 21
- 239000000203 mixture Substances 0.000 claims description 21
- 238000004821 distillation Methods 0.000 claims description 19
- 239000002904 solvent Substances 0.000 claims description 19
- 239000006227 byproduct Substances 0.000 claims description 15
- 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 claims description 12
- 239000012442 inert solvent Substances 0.000 claims description 10
- 238000002360 preparation method Methods 0.000 claims description 9
- 239000003377 acid catalyst Substances 0.000 claims description 8
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 claims description 8
- 238000011049 filling Methods 0.000 claims description 7
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 6
- 150000007513 acids Chemical class 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 claims description 4
- 125000004428 fluoroalkoxy group Chemical group 0.000 claims description 4
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 3
- 239000001301 oxygen Substances 0.000 claims description 3
- 229910052760 oxygen Inorganic materials 0.000 claims description 3
- JIRHAGAOHOYLNO-UHFFFAOYSA-N (3-cyclopentyloxy-4-methoxyphenyl)methanol Chemical compound COC1=CC=C(CO)C=C1OC1CCCC1 JIRHAGAOHOYLNO-UHFFFAOYSA-N 0.000 claims description 2
- MIOPJNTWMNEORI-GMSGAONNSA-N (S)-camphorsulfonic acid Chemical compound C1C[C@@]2(CS(O)(=O)=O)C(=O)C[C@@H]1C2(C)C MIOPJNTWMNEORI-GMSGAONNSA-N 0.000 claims description 2
- HTSGKJQDMSTCGS-UHFFFAOYSA-N 1,4-bis(4-chlorophenyl)-2-(4-methylphenyl)sulfonylbutane-1,4-dione Chemical compound C1=CC(C)=CC=C1S(=O)(=O)C(C(=O)C=1C=CC(Cl)=CC=1)CC(=O)C1=CC=C(Cl)C=C1 HTSGKJQDMSTCGS-UHFFFAOYSA-N 0.000 claims description 2
- 101100231508 Caenorhabditis elegans ceh-5 gene Proteins 0.000 claims description 2
- 229920001131 Pulp (paper) Polymers 0.000 claims description 2
- SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 claims description 2
- 229940092714 benzenesulfonic acid Drugs 0.000 claims description 2
- 230000003197 catalytic effect Effects 0.000 claims description 2
- 229940098779 methanesulfonic acid Drugs 0.000 claims description 2
- OWIUPIRUAQMTTK-UHFFFAOYSA-M n-aminocarbamate Chemical compound NNC([O-])=O OWIUPIRUAQMTTK-UHFFFAOYSA-M 0.000 claims description 2
- 230000006340 racemization Effects 0.000 claims description 2
- 241000238421 Arthropoda Species 0.000 claims 1
- 150000001990 dicarboxylic acid derivatives Chemical class 0.000 claims 1
- 230000002496 gastric effect Effects 0.000 claims 1
- BCQZXOMGPXTTIC-UHFFFAOYSA-N halothane Chemical compound FC(F)(F)C(Cl)Br BCQZXOMGPXTTIC-UHFFFAOYSA-N 0.000 claims 1
- 229960003132 halothane Drugs 0.000 claims 1
- 238000005984 hydrogenation reaction Methods 0.000 claims 1
- 239000002917 insecticide Substances 0.000 claims 1
- 238000004898 kneading Methods 0.000 claims 1
- 229940032330 sulfuric acid Drugs 0.000 claims 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 52
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 16
- 238000010992 reflux Methods 0.000 description 15
- 238000009835 boiling Methods 0.000 description 13
- 239000011541 reaction mixture Substances 0.000 description 13
- KLKFAASOGCDTDT-UHFFFAOYSA-N ethoxymethoxyethane Chemical compound CCOCOCC KLKFAASOGCDTDT-UHFFFAOYSA-N 0.000 description 10
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 210000003128 head Anatomy 0.000 description 8
- 229910052757 nitrogen Inorganic materials 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- 238000010438 heat treatment Methods 0.000 description 7
- 239000002002 slurry Substances 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 6
- 150000005063 oxadiazines Chemical class 0.000 description 6
- OWIUPIRUAQMTTK-UHFFFAOYSA-N carbazic acid Chemical class NNC(O)=O OWIUPIRUAQMTTK-UHFFFAOYSA-N 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 150000001298 alcohols Chemical class 0.000 description 4
- 239000000498 cooling water Substances 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
- KJIFKLIQANRMOU-UHFFFAOYSA-N oxidanium;4-methylbenzenesulfonate Chemical compound O.CC1=CC=C(S(O)(=O)=O)C=C1 KJIFKLIQANRMOU-UHFFFAOYSA-N 0.000 description 4
- 238000010025 steaming Methods 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 238000004128 high performance liquid chromatography Methods 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000002841 Lewis acid Substances 0.000 description 2
- 150000001335 aliphatic alkanes Chemical class 0.000 description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
- IVHKZGYFKJRXBD-UHFFFAOYSA-N amino carbamate Chemical compound NOC(N)=O IVHKZGYFKJRXBD-UHFFFAOYSA-N 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- LDECUSDQMXVUMP-UHFFFAOYSA-N benzyl 3-[6-[[2-(butylamino)-1-[3-methoxycarbonyl-4-(2-methoxy-2-oxoethoxy)phenyl]-2-oxoethyl]-hexylamino]-6-oxohexyl]-4-methyl-2-oxo-6-(4-phenylphenyl)-1,6-dihydropyrimidine-5-carboxylate Chemical compound O=C1NC(C=2C=CC(=CC=2)C=2C=CC=CC=2)C(C(=O)OCC=2C=CC=CC=2)=C(C)N1CCCCCC(=O)N(CCCCCC)C(C(=O)NCCCC)C1=CC=C(OCC(=O)OC)C(C(=O)OC)=C1 LDECUSDQMXVUMP-UHFFFAOYSA-N 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- CZZYITDELCSZES-UHFFFAOYSA-N diphenylmethane Chemical compound C=1C=CC=CC=1CC1=CC=CC=C1 CZZYITDELCSZES-UHFFFAOYSA-N 0.000 description 2
- -1 ethoxy, n-propoxy Chemical group 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 238000000855 fermentation Methods 0.000 description 2
- 230000004151 fermentation Effects 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 150000007517 lewis acids Chemical class 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- GETTZEONDQJALK-UHFFFAOYSA-N (trifluoromethyl)benzene Chemical compound FC(F)(F)C1=CC=CC=C1 GETTZEONDQJALK-UHFFFAOYSA-N 0.000 description 1
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- LBLYYCQCTBFVLH-UHFFFAOYSA-N 2-Methylbenzenesulfonic acid Chemical compound CC1=CC=CC=C1S(O)(=O)=O LBLYYCQCTBFVLH-UHFFFAOYSA-N 0.000 description 1
- BSTHYPUZLOXKTM-UHFFFAOYSA-N 2H-oxadiazine-4,5-dicarboxylic acid Chemical compound C1=C(C(=NNO1)C(=O)O)C(=O)O BSTHYPUZLOXKTM-UHFFFAOYSA-N 0.000 description 1
- 101100294106 Caenorhabditis elegans nhr-3 gene Proteins 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- IMNFDUFMRHMDMM-UHFFFAOYSA-N anhydrous n-heptane Natural products CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 238000003556 assay Methods 0.000 description 1
- 238000010533 azeotropic distillation Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- HRYZWHHZPQKTII-UHFFFAOYSA-N chloroethane Chemical compound CCCl HRYZWHHZPQKTII-UHFFFAOYSA-N 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000002079 cooperative effect Effects 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- NLFBCYMMUAKCPC-KQQUZDAGSA-N ethyl (e)-3-[3-amino-2-cyano-1-[(e)-3-ethoxy-3-oxoprop-1-enyl]sulfanyl-3-oxoprop-1-enyl]sulfanylprop-2-enoate Chemical group CCOC(=O)\C=C\SC(=C(C#N)C(N)=O)S\C=C\C(=O)OCC NLFBCYMMUAKCPC-KQQUZDAGSA-N 0.000 description 1
- 229960003750 ethyl chloride Drugs 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- VSXVVOUDAIVQOH-UHFFFAOYSA-K gold(3+) trifluoromethanesulfonate Chemical compound [Au+3].[O-]S(=O)(=O)C(F)(F)F.[O-]S(=O)(=O)C(F)(F)F.[O-]S(=O)(=O)C(F)(F)F VSXVVOUDAIVQOH-UHFFFAOYSA-K 0.000 description 1
- OAKJQQAXSVQMHS-UHFFFAOYSA-N hydrazine Substances NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 125000003253 isopropoxy group Chemical group [H]C([H])([H])C([H])(O*)C([H])([H])[H] 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- VMGAPWLDMVPYIA-HIDZBRGKSA-N n'-amino-n-iminomethanimidamide Chemical compound N\N=C\N=N VMGAPWLDMVPYIA-HIDZBRGKSA-N 0.000 description 1
- 125000006239 protecting group Chemical group 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- BOLDJAUMGUJJKM-LSDHHAIUSA-N renifolin D Natural products CC(=C)[C@@H]1Cc2c(O)c(O)ccc2[C@H]1CC(=O)c3ccc(O)cc3O BOLDJAUMGUJJKM-LSDHHAIUSA-N 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 125000002827 triflate group Chemical class FC(S(=O)(=O)O*)(F)F 0.000 description 1
- 238000012795 verification Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D273/00—Heterocyclic compounds containing rings having nitrogen and oxygen atoms as the only ring hetero atoms, not provided for by groups C07D261/00 - C07D271/00
- C07D273/02—Heterocyclic compounds containing rings having nitrogen and oxygen atoms as the only ring hetero atoms, not provided for by groups C07D261/00 - C07D271/00 having two nitrogen atoms and only one oxygen atom
- C07D273/04—Six-membered rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US2242696P | 1996-08-05 | 1996-08-05 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| TW337984B true TW337984B (en) | 1998-08-11 |
Family
ID=21809536
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW86108354A TW337984B (en) | 1996-08-05 | 1997-06-16 | Processes for preparing indeno{1,2-e}{1,3,4}oxadiazine-dicarboxylates |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | USH1950H1 (cg-RX-API-DMAC7.html) |
| EP (1) | EP0922041A1 (cg-RX-API-DMAC7.html) |
| JP (1) | JP2001501916A (cg-RX-API-DMAC7.html) |
| CN (1) | CN1226891A (cg-RX-API-DMAC7.html) |
| AU (1) | AU3903897A (cg-RX-API-DMAC7.html) |
| BR (1) | BR9711003A (cg-RX-API-DMAC7.html) |
| IN (1) | IN182799B (cg-RX-API-DMAC7.html) |
| TR (1) | TR199900224T2 (cg-RX-API-DMAC7.html) |
| TW (1) | TW337984B (cg-RX-API-DMAC7.html) |
| WO (1) | WO1998005656A1 (cg-RX-API-DMAC7.html) |
| ZA (1) | ZA975379B (cg-RX-API-DMAC7.html) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU4553999A (en) * | 1998-06-10 | 1999-12-30 | E.I. Du Pont De Nemours And Company | Arthropodicidal carboxanilides |
| JP4359500B2 (ja) | 2001-06-29 | 2009-11-04 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | ジルコニウム触媒によるβ−ジカルボニルのヒドロキシル化 |
| JP4537761B2 (ja) * | 2004-05-13 | 2010-09-08 | 築野食品工業株式会社 | トコトリエノール含有家禽卵 |
| BRPI0714900B8 (pt) | 2006-09-01 | 2017-05-30 | Du Pont | formulações tópicas locais spot-on |
| CN102391261A (zh) * | 2011-10-14 | 2012-03-28 | 上海交通大学 | 一种n-取代噁二嗪类化合物及其制备方法和应用 |
| CN104262285B (zh) * | 2014-07-24 | 2016-08-17 | 浙江大学 | 农用杀虫剂茚虫威中间体的合成法 |
| CN106397351B (zh) * | 2016-08-31 | 2018-10-30 | 京博农化科技股份有限公司 | 一种茚虫威中间体的制备方法 |
| CN108997254A (zh) * | 2018-08-27 | 2018-12-14 | 湖南国发精细化工科技有限公司 | 茚并噁二嗪化合物的合成方法 |
| CN113607833B (zh) * | 2021-07-08 | 2023-10-31 | 山东京博农化科技股份有限公司 | 一种茚虫威中间体的含量分析方法 |
| CN113607836B (zh) * | 2021-07-23 | 2023-10-31 | 山东京博农化科技股份有限公司 | 一种茚虫威关键中间体含量的分析方法 |
| IL313902A (en) | 2022-01-04 | 2024-08-01 | Adama Makhteshim Ltd | A process for the preparation of indoxacarb and its intermediates |
| CN114957158A (zh) * | 2022-05-31 | 2022-08-30 | 浙江禾本科技股份有限公司 | 一种制备茚虫威中间体的方法 |
| CN115974808B (zh) * | 2022-12-21 | 2024-03-12 | 大连奇凯医药科技有限公司 | 2-苄基-7-氯[1,2-e]茚并[1,3,4]噁二嗪二甲酸甲酯的制备方法 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5462938A (en) | 1990-12-21 | 1995-10-31 | Annus; Gary D. | Arthropodicidal oxadiazinyl, thiadiazinyl and triazinyl carboxanilides |
| US5500438A (en) * | 1991-05-24 | 1996-03-19 | E. I. Du Pont De Nemours And Company | Arthropodicidal anilides |
| JP3446052B2 (ja) | 1992-03-26 | 2003-09-16 | イー・アイ・デユポン・ドウ・ヌムール・アンド・カンパニー | 殺節足動物性アミド類 |
| DE69534440T2 (de) | 1994-04-20 | 2006-07-13 | E.I. Dupont De Nemours And Co., Wilmington | Indanone und Carbamat, und ihre Verwendung in der Herstellung von arthropoziden Oxadiazinen |
-
1997
- 1997-01-31 US US09/230,987 patent/USH1950H1/en not_active Abandoned
- 1997-06-02 IN IN1020CA1997 patent/IN182799B/en unknown
- 1997-06-16 TW TW86108354A patent/TW337984B/zh active
- 1997-06-18 ZA ZA975379A patent/ZA975379B/xx unknown
- 1997-07-31 BR BR9711003A patent/BR9711003A/pt not_active Application Discontinuation
- 1997-07-31 TR TR1999/00224T patent/TR199900224T2/xx unknown
- 1997-07-31 AU AU39038/97A patent/AU3903897A/en not_active Abandoned
- 1997-07-31 JP JP10508080A patent/JP2001501916A/ja active Pending
- 1997-07-31 WO PCT/US1997/013548 patent/WO1998005656A1/en not_active Ceased
- 1997-07-31 CN CN97196880A patent/CN1226891A/zh active Pending
- 1997-07-31 EP EP97936346A patent/EP0922041A1/en not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| BR9711003A (pt) | 1999-08-17 |
| MX9901054A (en) | 2000-01-01 |
| EP0922041A1 (en) | 1999-06-16 |
| JP2001501916A (ja) | 2001-02-13 |
| AU3903897A (en) | 1998-02-25 |
| TR199900224T2 (en) | 1999-04-21 |
| WO1998005656A1 (en) | 1998-02-12 |
| ZA975379B (en) | 1998-12-18 |
| USH1950H1 (en) | 2001-03-06 |
| CN1226891A (zh) | 1999-08-25 |
| IN182799B (cg-RX-API-DMAC7.html) | 1999-07-24 |
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