CN1384828A - 5-氯二氟甲基-1,3,4-噻二唑-2-基-氧乙酰苯胺 - Google Patents
5-氯二氟甲基-1,3,4-噻二唑-2-基-氧乙酰苯胺 Download PDFInfo
- Publication number
- CN1384828A CN1384828A CN00811044A CN00811044A CN1384828A CN 1384828 A CN1384828 A CN 1384828A CN 00811044 A CN00811044 A CN 00811044A CN 00811044 A CN00811044 A CN 00811044A CN 1384828 A CN1384828 A CN 1384828A
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- China
- Prior art keywords
- methyl
- group
- ethyl
- thiadiazoles
- chlorodifluoramethyl
- 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
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- 238000000034 method Methods 0.000 claims abstract description 18
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- ALZOLUNSQWINIR-UHFFFAOYSA-N quinmerac Chemical compound OC(=O)C1=C(Cl)C=CC2=CC(C)=CN=C21 ALZOLUNSQWINIR-UHFFFAOYSA-N 0.000 description 1
- OSUHJPCHFDQAIT-GFCCVEGCSA-N quizalofop-P-ethyl Chemical group C1=CC(O[C@H](C)C(=O)OCC)=CC=C1OC1=CN=C(C=C(Cl)C=C2)C2=N1 OSUHJPCHFDQAIT-GFCCVEGCSA-N 0.000 description 1
- BACHBFVBHLGWSL-JTQLQIEISA-N rac-diclofop methyl Natural products C1=CC(O[C@@H](C)C(=O)OC)=CC=C1OC1=CC=C(Cl)C=C1Cl BACHBFVBHLGWSL-JTQLQIEISA-N 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 230000002940 repellent Effects 0.000 description 1
- 230000001850 reproductive effect Effects 0.000 description 1
- MEFOUWRMVYJCQC-UHFFFAOYSA-N rimsulfuron Chemical compound CCS(=O)(=O)C1=CC=CN=C1S(=O)(=O)NC(=O)NC1=NC(OC)=CC(OC)=N1 MEFOUWRMVYJCQC-UHFFFAOYSA-N 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- LMHHRCOWPQNFTF-UHFFFAOYSA-N s-propan-2-yl azepane-1-carbothioate Chemical compound CC(C)SC(=O)N1CCCCCC1 LMHHRCOWPQNFTF-UHFFFAOYSA-N 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910052624 sepiolite Inorganic materials 0.000 description 1
- 235000019355 sepiolite Nutrition 0.000 description 1
- 230000001568 sexual effect Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229960001866 silicon dioxide Drugs 0.000 description 1
- ODCWYMIRDDJXKW-UHFFFAOYSA-N simazine Chemical compound CCNC1=NC(Cl)=NC(NCC)=N1 ODCWYMIRDDJXKW-UHFFFAOYSA-N 0.000 description 1
- MGLWZSOBALDPEK-UHFFFAOYSA-N simetryn Chemical compound CCNC1=NC(NCC)=NC(SC)=N1 MGLWZSOBALDPEK-UHFFFAOYSA-N 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- ODZPKZBBUMBTMG-UHFFFAOYSA-N sodium amide Chemical compound [NH2-].[Na+] ODZPKZBBUMBTMG-UHFFFAOYSA-N 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical compound [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 1
- 239000012312 sodium hydride Substances 0.000 description 1
- 229910000104 sodium hydride Inorganic materials 0.000 description 1
- 239000003516 soil conditioner Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 238000000967 suction filtration Methods 0.000 description 1
- OORLZFUTLGXMEF-UHFFFAOYSA-N sulfentrazone Chemical compound O=C1N(C(F)F)C(C)=NN1C1=CC(NS(C)(=O)=O)=C(Cl)C=C1Cl OORLZFUTLGXMEF-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- ZDXMLEQEMNLCQG-UHFFFAOYSA-N sulfometuron methyl Chemical group COC(=O)C1=CC=CC=C1S(=O)(=O)NC(=O)NC1=NC(C)=CC(C)=N1 ZDXMLEQEMNLCQG-UHFFFAOYSA-N 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- RJKCKKDSSSRYCB-UHFFFAOYSA-N tebutam Chemical compound CC(C)(C)C(=O)N(C(C)C)CC1=CC=CC=C1 RJKCKKDSSSRYCB-UHFFFAOYSA-N 0.000 description 1
- IROINLKCQGIITA-UHFFFAOYSA-N terbutryn Chemical compound CCNC1=NC(NC(C)(C)C)=NC(SC)=N1 IROINLKCQGIITA-UHFFFAOYSA-N 0.000 description 1
- FZXISNSWEXTPMF-UHFFFAOYSA-N terbutylazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)(C)C)=N1 FZXISNSWEXTPMF-UHFFFAOYSA-N 0.000 description 1
- ZFXYFBGIUFBOJW-UHFFFAOYSA-N theophylline Chemical compound O=C1N(C)C(=O)N(C)C2=C1NC=N2 ZFXYFBGIUFBOJW-UHFFFAOYSA-N 0.000 description 1
- 229960000278 theophylline Drugs 0.000 description 1
- AHTPATJNIAFOLR-UHFFFAOYSA-N thifensulfuron-methyl Chemical group S1C=CC(S(=O)(=O)NC(=O)NC=2N=C(OC)N=C(C)N=2)=C1C(=O)OC AHTPATJNIAFOLR-UHFFFAOYSA-N 0.000 description 1
- DLFVBJFMPXGRIB-UHFFFAOYSA-N thioacetamide Natural products CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- DQFPEYARZIQXRM-LTGZKZEYSA-N tralkoxydim Chemical compound C1C(=O)C(C(/CC)=N/OCC)=C(O)CC1C1=C(C)C=C(C)C=C1C DQFPEYARZIQXRM-LTGZKZEYSA-N 0.000 description 1
- 230000009261 transgenic effect Effects 0.000 description 1
- 235000011351 tree mallow Nutrition 0.000 description 1
- XOPFESVZMSQIKC-UHFFFAOYSA-N triasulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)OCCCl)=N1 XOPFESVZMSQIKC-UHFFFAOYSA-N 0.000 description 1
- YMXOXAPKZDWXLY-QWRGUYRKSA-N tribenuron methyl Chemical group COC(=O)[C@H]1CCCC[C@@H]1S(=O)(=O)NC(=O)N(C)C1=NC(C)=NC(OC)=N1 YMXOXAPKZDWXLY-QWRGUYRKSA-N 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- REEQLXCGVXDJSQ-UHFFFAOYSA-N trichlopyr Chemical compound OC(=O)COC1=NC(Cl)=C(Cl)C=C1Cl REEQLXCGVXDJSQ-UHFFFAOYSA-N 0.000 description 1
- ZSDSQXJSNMTJDA-UHFFFAOYSA-N trifluralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-N 0.000 description 1
- IMEVJVISCHQJRM-UHFFFAOYSA-N triflusulfuron-methyl Chemical group COC(=O)C1=CC=CC(C)=C1S(=O)(=O)NC(=O)NC1=NC(OCC(F)(F)F)=NC(N(C)C)=N1 IMEVJVISCHQJRM-UHFFFAOYSA-N 0.000 description 1
- YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
- 241000228158 x Triticosecale Species 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D285/00—Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
- C07D285/01—Five-membered rings
- C07D285/02—Thiadiazoles; Hydrogenated thiadiazoles
- C07D285/04—Thiadiazoles; Hydrogenated thiadiazoles not condensed with other rings
- C07D285/12—1,3,4-Thiadiazoles; Hydrogenated 1,3,4-thiadiazoles
- C07D285/125—1,3,4-Thiadiazoles; Hydrogenated 1,3,4-thiadiazoles with oxygen, sulfur or nitrogen atoms, directly attached to ring carbon atoms, the nitrogen atoms not forming part of a nitro radical
- C07D285/13—Oxygen 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
- A01N25/04—Dispersions, emulsions, suspoemulsions, suspension concentrates or gels
-
- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/82—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with three ring hetero atoms
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Environmental Sciences (AREA)
- Dentistry (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Dispersion Chemistry (AREA)
- Toxicology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Description
实施例号 | R | (位置)Xn | 理化常数 |
2 | i-C3H7 | (4)Cl | 熔点:78℃ |
3 | i-C3H7 | (3)Cl | 熔点:71℃ |
4 | i-C3H7 | (3)CH3 | 熔点:57℃ |
5 | i-C3H7 | (4)CH3 | 熔点:78℃ |
6 | i-C3H7 | (3)OCH3 | 熔点:79℃ |
7 | i-C3H7 | (3)F | 熔点:60℃ |
8 | i-CxH7 | (2,4)F2 | 熔点:84℃ |
Claims (8)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19935964.4 | 1999-07-30 | ||
DE19935964A DE19935964A1 (de) | 1999-07-30 | 1999-07-30 | 5-Chlordifluormethyl-1,3,4-thiadiazol-2-yl-oxyacetanilide |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1384828A true CN1384828A (zh) | 2002-12-11 |
CN1213039C CN1213039C (zh) | 2005-08-03 |
Family
ID=7916664
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CNB008110441A Expired - Lifetime CN1213039C (zh) | 1999-07-30 | 2000-07-18 | 5-氯二氟甲基-1,3,4-噻二唑-2-基-氧乙酰苯胺 |
Country Status (16)
Country | Link |
---|---|
US (1) | US6602827B1 (zh) |
EP (1) | EP1204651B1 (zh) |
JP (1) | JP4936622B2 (zh) |
KR (1) | KR100687181B1 (zh) |
CN (1) | CN1213039C (zh) |
AT (1) | ATE340169T1 (zh) |
AU (1) | AU769586B2 (zh) |
BR (1) | BR0012838B1 (zh) |
CA (1) | CA2380958C (zh) |
DE (2) | DE19935964A1 (zh) |
DK (1) | DK1204651T3 (zh) |
ES (1) | ES2270860T3 (zh) |
MX (1) | MXPA02001015A (zh) |
PL (1) | PL200669B1 (zh) |
RU (1) | RU2245333C2 (zh) |
WO (1) | WO2001009109A1 (zh) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2014121439A1 (zh) * | 2013-02-05 | 2014-08-14 | 浙江省诸暨合力化学对外贸易有限公司 | 噻二唑酰胺衍生物合成方法 |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3400168A1 (de) | 1984-01-04 | 1985-07-11 | Bayer Ag, 5090 Leverkusen | 5-halogenalkyl-1,3,4-thiadiazol-2-yloxyacetamide |
DE3418167A1 (de) * | 1984-05-16 | 1985-11-21 | Bayer Ag, 5090 Leverkusen | Verwendung von amiden zur verbesserung der kulturpflanzen-vertraeglichkeit von herbizid wirksamen heteroaryloxyacetamiden |
DE3422861A1 (de) | 1984-06-20 | 1986-01-02 | Bayer Ag, 5090 Leverkusen | Verfahren zur herstellung von heteroaryloxyacetamiden |
US5177090A (en) | 1987-07-07 | 1993-01-05 | Bayer Aktiengesellschaft | Microbicidal agents |
DE3722320A1 (de) | 1987-07-07 | 1989-01-19 | Bayer Ag | Mikrobizide mittel |
DE3731803A1 (de) | 1987-09-22 | 1989-03-30 | Bayer Ag | Verfahren zur herstellung von 2,4-dichlor-5-dichlormethyl-thiazol |
DE3821600A1 (de) * | 1988-06-27 | 1989-12-28 | Bayer Ag | Heteroaryloxyessigsaeure-n-isopropylanilide |
DE3821597A1 (de) * | 1988-06-27 | 1989-12-28 | Bayer Ag | 5-difluormethyl-1,3,4-thiadiazol-2-yl- oxyessigsaeureamide, verfahren und 5-difluormethyl-2- methylsulfonyl- bzw. 2- methylthio-1,3,4-thiadiazol als zwischenprodukte zu ihrer herstellung und ihre verwendung als selektivherbizide |
DE3821598A1 (de) | 1988-06-27 | 1989-12-28 | Bayer Ag | 5-chlor-4-cyano-thiazol-2-yl-oxyessigsaeureamide |
DE4317323A1 (de) * | 1993-05-25 | 1994-12-01 | Bayer Ag | N-(4-Fluor-phenyl)-heteroaryloxyacetamide |
DE19933936A1 (de) * | 1999-07-20 | 2001-01-25 | Bayer Ag | Substituierte Heteroaryloxyacetanilide |
-
1999
- 1999-07-30 DE DE19935964A patent/DE19935964A1/de not_active Withdrawn
-
2000
- 2000-07-18 AT AT00951397T patent/ATE340169T1/de active
- 2000-07-18 DK DK00951397T patent/DK1204651T3/da active
- 2000-07-18 RU RU2002105514/04A patent/RU2245333C2/ru active
- 2000-07-18 PL PL362902A patent/PL200669B1/pl unknown
- 2000-07-18 CN CNB008110441A patent/CN1213039C/zh not_active Expired - Lifetime
- 2000-07-18 MX MXPA02001015A patent/MXPA02001015A/es active IP Right Grant
- 2000-07-18 CA CA002380958A patent/CA2380958C/en not_active Expired - Lifetime
- 2000-07-18 US US10/048,088 patent/US6602827B1/en not_active Expired - Lifetime
- 2000-07-18 WO PCT/EP2000/006851 patent/WO2001009109A1/de active IP Right Grant
- 2000-07-18 JP JP2001514312A patent/JP4936622B2/ja not_active Expired - Fee Related
- 2000-07-18 AU AU64352/00A patent/AU769586B2/en not_active Expired
- 2000-07-18 DE DE50013499T patent/DE50013499D1/de not_active Expired - Lifetime
- 2000-07-18 KR KR1020027000560A patent/KR100687181B1/ko active IP Right Grant
- 2000-07-18 EP EP00951397A patent/EP1204651B1/de not_active Expired - Lifetime
- 2000-07-18 BR BRPI0012838-4A patent/BR0012838B1/pt not_active IP Right Cessation
- 2000-07-18 ES ES00951397T patent/ES2270860T3/es not_active Expired - Lifetime
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2014121439A1 (zh) * | 2013-02-05 | 2014-08-14 | 浙江省诸暨合力化学对外贸易有限公司 | 噻二唑酰胺衍生物合成方法 |
Also Published As
Publication number | Publication date |
---|---|
RU2245333C2 (ru) | 2005-01-27 |
PL200669B1 (pl) | 2009-01-30 |
ATE340169T1 (de) | 2006-10-15 |
US6602827B1 (en) | 2003-08-05 |
EP1204651B1 (de) | 2006-09-20 |
KR100687181B1 (ko) | 2007-02-27 |
KR20020091043A (ko) | 2002-12-05 |
ES2270860T3 (es) | 2007-04-16 |
AU769586B2 (en) | 2004-01-29 |
EP1204651A1 (de) | 2002-05-15 |
CA2380958A1 (en) | 2001-02-08 |
CA2380958C (en) | 2009-05-19 |
DE50013499D1 (de) | 2006-11-02 |
PL362902A1 (en) | 2004-11-02 |
BR0012838A (pt) | 2002-04-30 |
AU6435200A (en) | 2001-02-19 |
BR0012838B1 (pt) | 2011-05-17 |
JP2003528809A (ja) | 2003-09-30 |
MXPA02001015A (es) | 2002-10-31 |
DE19935964A1 (de) | 2001-02-01 |
DK1204651T3 (da) | 2007-01-29 |
CN1213039C (zh) | 2005-08-03 |
WO2001009109A1 (de) | 2001-02-08 |
JP4936622B2 (ja) | 2012-05-23 |
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