IL29091A - תולדות 2-)אנילינוקרבוניל(- איזאוקסאזולידין והכנתן - Google Patents

תולדות 2-)אנילינוקרבוניל(- איזאוקסאזולידין והכנתן

Info

Publication number: IL29091A
Authority: IL; Israel
Prior art keywords: compounds; compound; general formula; isoxazolidine; compositions
Prior art date: 1966-12-09

Application number

IL29091A

Other languages

English (en)

Original Assignee

Boehringer Sohn Ingelheim

Priority date (The priority date 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 date listed.)

1966-12-09

Filing date

1967-12-08

Publication date

1972-01-27

1967-12-08 Application filed by Boehringer Sohn Ingelheim filed Critical Boehringer Sohn Ingelheim

1972-01-27 Publication of IL29091A publication Critical patent/IL29091A/he

Links

238000002360 preparation method Methods 0.000 title claims description 6
LWRPZEXAYVOBMG-UHFFFAOYSA-N N-phenyl-1,2-oxazolidine-2-carboxamide Chemical class N(C1=CC=CC=C1)C(=O)N1OCCC1 LWRPZEXAYVOBMG-UHFFFAOYSA-N 0.000 title claims 2
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 36
150000001875 compounds Chemical class 0.000 claims description 29
239000000203 mixture Substances 0.000 claims description 14
238000000034 method Methods 0.000 claims description 11
238000006243 chemical reaction Methods 0.000 claims description 10
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 9
230000002363 herbicidal effect Effects 0.000 claims description 6
-1 2-(3-Chloroanilinocarbonyl)-isoxazolidine Chemical compound 0.000 claims description 4
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
239000011149 active material Substances 0.000 claims description 4
229910052736 halogen Inorganic materials 0.000 claims description 4
150000002367 halogens Chemical group 0.000 claims description 4
229910052739 hydrogen Inorganic materials 0.000 claims description 4
239000001257 hydrogen Substances 0.000 claims description 4
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 3
239000003085 diluting agent Substances 0.000 claims description 3
238000010410 dusting Methods 0.000 claims description 3
239000000839 emulsion Substances 0.000 claims description 3
229910052740 iodine Inorganic materials 0.000 claims description 3
239000000843 powder Substances 0.000 claims description 3
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
239000004606 Fillers/Extenders Substances 0.000 claims description 2
QZRGKCOWNLSUDK-UHFFFAOYSA-N Iodochlorine Chemical compound ICl QZRGKCOWNLSUDK-UHFFFAOYSA-N 0.000 claims description 2
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
229910052794 bromium Inorganic materials 0.000 claims description 2
239000003795 chemical substances by application Substances 0.000 claims description 2
239000003960 organic solvent Substances 0.000 claims description 2
125000000951 phenoxy group Chemical class [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 2
239000002904 solvent Substances 0.000 claims description 2
125000001424 substituent group Chemical group 0.000 claims description 2
239000000725 suspension Substances 0.000 claims description 2
239000000080 wetting agent Substances 0.000 claims description 2
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 2
229910052801 chlorine Inorganic materials 0.000 claims 2
239000000460 chlorine Substances 0.000 claims 2
101100381997 Danio rerio tbc1d32 gene Proteins 0.000 claims 1
101100381999 Mus musculus Tbc1d32 gene Proteins 0.000 claims 1
BHNBOEUGRLMSPR-UHFFFAOYSA-N N-(3,4-dichlorophenyl)-1,2-oxazolidine-2-carboxamide Chemical compound ClC1=C(Cl)C=C(NC(=O)N2CCCO2)C=C1 BHNBOEUGRLMSPR-UHFFFAOYSA-N 0.000 claims 1
ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims 1
125000003545 alkoxy group Chemical group 0.000 claims 1
125000000217 alkyl group Chemical group 0.000 claims 1
125000004432 carbon atom Chemical group C* 0.000 claims 1
239000003995 emulsifying agent Substances 0.000 claims 1
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 1
125000001033 ether group Chemical group 0.000 claims 1
125000005843 halogen group Chemical group 0.000 claims 1
239000004009 herbicide Substances 0.000 claims 1
239000007921 spray Substances 0.000 claims 1
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
CIISBYKBBMFLEZ-UHFFFAOYSA-N 1,2-oxazolidine Chemical compound C1CNOC1 CIISBYKBBMFLEZ-UHFFFAOYSA-N 0.000 description 8
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 4
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 4
238000009472 formulation Methods 0.000 description 4
229910052708 sodium Inorganic materials 0.000 description 4
239000011734 sodium Substances 0.000 description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
239000002244 precipitate Substances 0.000 description 3
238000001953 recrystallisation Methods 0.000 description 3
238000003756 stirring Methods 0.000 description 3
125000000446 sulfanediyl group Chemical group *S* 0.000 description 3
HPIVVOQIZYNVJE-UHFFFAOYSA-N 1,2-oxazolidin-2-ium;chloride Chemical compound Cl.C1CNOC1 HPIVVOQIZYNVJE-UHFFFAOYSA-N 0.000 description 2
239000005995 Aluminium silicate Substances 0.000 description 2
PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
229960000583 acetic acid Drugs 0.000 description 2
239000013543 active substance Substances 0.000 description 2
235000012211 aluminium silicate Nutrition 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
239000012362 glacial acetic acid Substances 0.000 description 2
239000012948 isocyanate Substances 0.000 description 2
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 2
239000010410 layer Substances 0.000 description 2
239000012044 organic layer Substances 0.000 description 2
DGTNSSLYPYDJGL-UHFFFAOYSA-N phenyl isocyanate Chemical compound O=C=NC1=CC=CC=C1 DGTNSSLYPYDJGL-UHFFFAOYSA-N 0.000 description 2
239000000047 product Substances 0.000 description 2
239000011541 reaction mixture Substances 0.000 description 2
239000000126 substance Substances 0.000 description 2
235000005781 Avena Nutrition 0.000 description 1
244000075850 Avena orientalis Species 0.000 description 1
241000196324 Embryophyta Species 0.000 description 1
244000110797 Polygonum persicaria Species 0.000 description 1
235000004442 Polygonum persicaria Nutrition 0.000 description 1
VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
240000006694 Stellaria media Species 0.000 description 1
244000274883 Urtica dioica Species 0.000 description 1
235000009108 Urtica dioica Nutrition 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
125000004414 alkyl thio group Chemical group 0.000 description 1
MMCPOSDMTGQNKG-UHFFFAOYSA-N anilinium chloride Chemical compound Cl.NC1=CC=CC=C1 MMCPOSDMTGQNKG-UHFFFAOYSA-N 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
238000001816 cooling Methods 0.000 description 1
230000001804 emulsifying effect Effects 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
239000000706 filtrate Substances 0.000 description 1
238000001914 filtration Methods 0.000 description 1
239000011630 iodine Substances 0.000 description 1
150000002513 isocyanates Chemical class 0.000 description 1
239000007788 liquid Substances 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
239000012429 reaction media Substances 0.000 description 1
239000001632 sodium acetate Substances 0.000 description 1
235000017281 sodium acetate Nutrition 0.000 description 1
239000007858 starting material Substances 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
150000003672 ureas Chemical class 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/38—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< where at least one nitrogen atom is part of a heterocyclic ring; Thio analogues thereof
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D265/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom and one oxygen atom as the only ring hetero atoms
- C07D265/02—1,2-Oxazines; Hydrogenated 1,2-oxazines

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)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

IL29091A 1966-12-09 1967-12-08 תולדות 2-)אנילינוקרבוניל(- איזאוקסאזולידין והכנתן IL29091A (he)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
DEB0090229		1966-12-09
DEB0092616		1967-05-19
DEB0092677		1967-05-23

Publications (1)

Publication Number	Publication Date
IL29091A true IL29091A (he)	1972-01-27

Family

ID=27209406

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL29091A IL29091A (he)	1966-12-09	1967-12-08	תולדות 2-)אנילינוקרבוניל(- איזאוקסאזולידין והכנתן

Country Status (8)

Country	Link
US (1)	US3560517A (he)
BE (1)	BE707752A (he)
CH (1)	CH515679A (he)
DE (3)	DE1670172C3 (he)
FR (1)	FR1560344A (he)
GB (1)	GB1177129A (he)
IL (1)	IL29091A (he)
NL (1)	NL6716744A (he)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3914121A (en) *	1969-12-18	1975-10-21	Gulf Research Development Co	Selectively herbicidal 2-substituted -4H-3,1-benzoxazin-4-ones
FR2085644B1 (he) *	1970-04-22	1973-06-08	Roussel Uclaf
US4060402A (en) *	1972-10-19	1977-11-29	Sankyo Company Limited	Isoxazolone derivatives, their preparation and their use as plant growth regulators
DE2948704A1 (de)	1979-12-04	1981-06-11	Basf Ag, 6700 Ludwigshafen	N-substituierte 2-methylnaphthylamide, verfahren zu ihrer herstellung und diese enthaltende fungizide
DE3246847A1 (de) *	1981-12-18	1983-06-30	Hokko Chemical Industry Co. Ltd., Tokyo	2-(substituiertes-phenoxy)-propionsaeurederivate, verfahren zur inhibierung des pflanzenwachstums und herbizide zusammensetzung

1966
- 1966-12-09 DE DE1670172A patent/DE1670172C3/de not_active Expired
1967
- 1967-05-19 DE DE19671670227 patent/DE1670227A1/de active Pending
- 1967-05-23 DE DE19671670229 patent/DE1670229A1/de active Pending
- 1967-12-06 US US688319A patent/US3560517A/en not_active Expired - Lifetime
- 1967-12-06 CH CH1707267A patent/CH515679A/de not_active IP Right Cessation
- 1967-12-08 GB GB56037/67A patent/GB1177129A/en not_active Expired
- 1967-12-08 BE BE707752D patent/BE707752A/xx unknown
- 1967-12-08 IL IL29091A patent/IL29091A/he unknown
- 1967-12-08 NL NL6716744A patent/NL6716744A/xx unknown
- 1967-12-08 FR FR1560344D patent/FR1560344A/fr not_active Expired

Also Published As

Publication number	Publication date
DE1670227A1 (de)	1970-08-13
DE1670172C3 (de)	1974-04-04
CH515679A (de)	1971-11-30
FR1560344A (he)	1969-03-21
DE1670172B2 (de)	1973-08-23
DE1670172A1 (de)	1970-04-23
US3560517A (en)	1971-02-02
DE1670229A1 (de)	1970-08-13
BE707752A (he)	1968-06-10
GB1177129A (en)	1970-01-07
NL6716744A (he)	1968-06-10

Publication	Publication Date	Title
US3882142A (en)	1975-05-06	1,2-Dialkyl-3,5-diphenyl pyrazolium salts
JPH02501831A (ja)	1990-06-21	複素環化合物
US4364875A (en)	1982-12-21	Process for the preparation of certain diphenyl ethers
IL44710A (en)	1977-12-30	1-phenyl-2-azolyl-formamidines their preparation and their use as herbicides
US3922161A (en)	1975-11-25	Novel herbicidal compositions
IL29091A (he)	1972-01-27	תולדות 2-)אנילינוקרבוניל(- איזאוקסאזולידין והכנתן
US4098894A (en)	1978-07-04	Triphenyl-1,2,3-triazolyl-(1)-methanes, and compositions and methods for combating fungi and bacteria employing them
US3867403A (en)	1975-02-18	1,2-dialkyl-3,5-diphenylpyrazolium salts
CS212721B2 (en)	1982-03-26	Fungicide and method of preparing effective components
US4170464A (en)	1979-10-09	Herbicidal combinations
US3427318A (en)	1969-02-11	Certain 2-alkanoylamino-5-halothiazoles
CA1249601A (en)	1989-01-31	Process for the preparation of substituted phenylhydrazines
EP0109575A2 (de)	1984-05-30	Benzoesäurederivate, Verfahren und Mittel zu deren Herstellung
US3857692A (en)	1974-12-31	1,2-dimethyl-3,5-diphenylpyrazolium salts and 3,5-dibromo-4-hydroxybenzonitrile herbicidal compositions
DE2932305C2 (he)	1990-03-22
US3973028A (en)	1976-08-03	1-Dimethylcarbamyl-3-branched alkyl-1,2,4-triazol-5-yl-(N-substituted) sulfonamides and use as insecticides
US4033960A (en)	1977-07-05	2-Mercaptoquinoxaline-di-N-oxide products and a method for their preparation
US2910463A (en)	1959-10-27	Phenylazo formamides and production thereof
US4034104A (en)	1977-07-05	Carbamic acid esters of gallic acid, their esters, and heavy metal salts
CA1050980A (en)	1979-03-20	1-alkylideneaminouracils, process for their preparation and their use as herbicides
EP0358018A2 (de)	1990-03-14	Verfahren zur Herstellung von Oxyguanidinen
DE2124260A1 (de)	1972-11-30	Verfahren zur Herstellung von 4 sub stituierten 1,3,4 Thiadiazolon (5) yl (2) harnstoffen
EP0473980A1 (de)	1992-03-11	Verfahren zur Herstellung von 3-Alkoxy-2-heteroazolylaminoacrylsäureestern
EP0352638B1 (de)	1995-02-22	5-Amino-6-pyridazonderivate, Verfahren zu ihrer Herstellung und sie enthaltende herbizide Mittel
EP0264019A2 (de)	1988-04-20	Verfahren zur Herstellung von Sulfonylisothioharnstoffen