CA1249512A - Compose pharmaceutique ou pesticide contenant du sulfoxyde de nitraminodiaryl - Google Patents

Compose pharmaceutique ou pesticide contenant du sulfoxyde de nitraminodiaryl

Info

Publication number: CA1249512A
Authority: CA; Canada
Prior art keywords: sulfoxide; nitrophenyl; phenyl; formula; chloro
Prior art date: 1984-02-29
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.): Expired

Application number

CA000545227A

Other languages

English (en)

Inventor

Janos Kreidl

Peter Turcsanyi

Bela Stefko

Judit Nee Brill Meszaros

Erik Bogsch

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Richter Gedeon Vegyeszeti Gyar Nyrt

Original Assignee

Richter Gedeon Vegyeszeti Gyar RT

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.)

1984-02-29

Filing date

1987-08-24

Publication date

1989-01-31

1984-02-29 Priority claimed from HU84814A external-priority patent/HU195950B/hu

1987-08-24 Application filed by Richter Gedeon Vegyeszeti Gyar RT filed Critical Richter Gedeon Vegyeszeti Gyar RT

1987-08-24 Priority to CA000545227A priority Critical patent/CA1249512A/fr

1989-01-31 Application granted granted Critical

1989-01-31 Publication of CA1249512A publication Critical patent/CA1249512A/fr

Status Expired legal-status Critical Current

Links

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150000003462 sulfoxides Chemical class 0.000 title claims abstract description 16
230000000361 pesticidal effect Effects 0.000 title claims abstract description 13
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229910052739 hydrogen Inorganic materials 0.000 claims abstract description 18
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125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 10
150000003839 salts Chemical class 0.000 claims abstract description 7
239000003085 diluting agent Substances 0.000 claims abstract 4
239000008194 pharmaceutical composition Substances 0.000 claims description 6
150000001875 compounds Chemical class 0.000 description 30
238000000034 method Methods 0.000 description 26
-1 methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy Chemical group 0.000 description 21
238000002844 melting Methods 0.000 description 18
230000008018 melting Effects 0.000 description 18
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239000007858 starting material Substances 0.000 description 15
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239000004088 foaming agent Substances 0.000 description 2
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HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 2
239000003960 organic solvent Substances 0.000 description 2
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125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 2
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IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
230000000802 nitrating effect Effects 0.000 description 1
JCZMXVGQBBATMY-UHFFFAOYSA-N nitro acetate Chemical compound CC(=O)O[N+]([O-])=O JCZMXVGQBBATMY-UHFFFAOYSA-N 0.000 description 1
150000002828 nitro derivatives Chemical class 0.000 description 1
JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 1
LYGJENNIWJXYER-UHFFFAOYSA-N nitromethane Chemical compound C[N+]([O-])=O LYGJENNIWJXYER-UHFFFAOYSA-N 0.000 description 1
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239000012860 organic pigment Substances 0.000 description 1
230000003204 osmotic effect Effects 0.000 description 1
BEZZFPOZAYTVHN-UHFFFAOYSA-N oxfendazole Chemical compound C=1C=C2NC(NC(=O)OC)=NC2=CC=1S(=O)C1=CC=CC=C1 BEZZFPOZAYTVHN-UHFFFAOYSA-N 0.000 description 1
230000001590 oxidative effect Effects 0.000 description 1
125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 description 1
229910052625 palygorskite Inorganic materials 0.000 description 1
235000020232 peanut Nutrition 0.000 description 1
239000001814 pectin Substances 0.000 description 1
235000010987 pectin Nutrition 0.000 description 1
229920001277 pectin Polymers 0.000 description 1
239000000575 pesticide Substances 0.000 description 1
IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
239000006187 pill Substances 0.000 description 1
239000002798 polar solvent Substances 0.000 description 1
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229920002451 polyvinyl alcohol Polymers 0.000 description 1
239000003755 preservative agent Substances 0.000 description 1
238000003825 pressing Methods 0.000 description 1
239000001294 propane Substances 0.000 description 1
239000003380 propellant Substances 0.000 description 1
QLNJFJADRCOGBJ-UHFFFAOYSA-N propionamide Chemical compound CCC(N)=O QLNJFJADRCOGBJ-UHFFFAOYSA-N 0.000 description 1
239000003531 protein hydrolysate Substances 0.000 description 1
239000008262 pumice Substances 0.000 description 1
238000000746 purification Methods 0.000 description 1
239000010453 quartz Substances 0.000 description 1
239000011435 rock Substances 0.000 description 1
229910052624 sepiolite Inorganic materials 0.000 description 1
235000019355 sepiolite Nutrition 0.000 description 1
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150000004760 silicates Chemical class 0.000 description 1
RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
239000000779 smoke Substances 0.000 description 1
239000008107 starch Substances 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
230000001954 sterilising effect Effects 0.000 description 1
238000004659 sterilization and disinfection Methods 0.000 description 1
238000006467 substitution reaction Methods 0.000 description 1
BUUPQKDIAURBJP-UHFFFAOYSA-N sulfinic acid Chemical compound OS=O BUUPQKDIAURBJP-UHFFFAOYSA-N 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
125000004434 sulfur atom Chemical group 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
RGKBHCHHMKMETO-UHFFFAOYSA-N sulfurous diamide Chemical class NS(N)=O RGKBHCHHMKMETO-UHFFFAOYSA-N 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
229920002994 synthetic fiber Polymers 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
YBRBMKDOPFTVDT-UHFFFAOYSA-N tert-butylamine Chemical compound CC(C)(C)N YBRBMKDOPFTVDT-UHFFFAOYSA-N 0.000 description 1
230000001225 therapeutic effect Effects 0.000 description 1
238000002560 therapeutic procedure Methods 0.000 description 1
238000004809 thin layer chromatography Methods 0.000 description 1
239000004408 titanium dioxide Substances 0.000 description 1
238000011282 treatment Methods 0.000 description 1
229940099259 vaseline Drugs 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
239000008158 vegetable oil Substances 0.000 description 1
239000002699 waste material Substances 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
239000008096 xylene Substances 0.000 description 1
150000003751 zinc Chemical class 0.000 description 1

Landscapes

Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

CA000545227A 1984-02-29 1987-08-24 Compose pharmaceutique ou pesticide contenant du sulfoxyde de nitraminodiaryl Expired CA1249512A (fr)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
CA000545227A CA1249512A (fr)	1984-02-29	1987-08-24	Compose pharmaceutique ou pesticide contenant du sulfoxyde de nitraminodiaryl

Applications Claiming Priority (4)

Application Number	Priority Date	Filing Date	Title
HU814/84		1984-02-29
HU84814A HU195950B (en)	1984-02-29	1984-02-29	Process for producing nitramino-diaryl-sulfoxide derivatives and pharmaceutics comprising such compounds
CA000475292A CA1261353A (fr)	1984-02-29	1985-02-27	Derives de sulfoxyde de nitraminodiaryle; methode de preparation; compositions pharmaceutiques et pesticides qui en renferment
CA000545227A CA1249512A (fr)	1984-02-29	1987-08-24	Compose pharmaceutique ou pesticide contenant du sulfoxyde de nitraminodiaryl

Related Parent Applications (1)

Application Number	Title	Priority Date	Filing Date
CA000475292A Division CA1261353A (fr)	1984-02-29	1985-02-27	Derives de sulfoxyde de nitraminodiaryle; methode de preparation; compositions pharmaceutiques et pesticides qui en renferment

Publications (1)

Publication Number	Publication Date
CA1249512A true CA1249512A (fr)	1989-01-31

Family

ID=25670600

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA000545227A Expired CA1249512A (fr)	1984-02-29	1987-08-24	Compose pharmaceutique ou pesticide contenant du sulfoxyde de nitraminodiaryl

Country Status (1)

Country	Link
CA (1)	CA1249512A (fr)

1987
- 1987-08-24 CA CA000545227A patent/CA1249512A/fr not_active Expired

Legal Events

Date	Code	Title	Description
2006-01-31	MKEX	Expiry

Publication	Publication Date	Title
EP0148725A1 (fr)	1985-07-17	Dérivés de sulfonamido-benzamides
US4831194A (en)	1989-05-16	Process for the preparation of nitrodiaryl sulfoxides
CA1249512A (fr)	1989-01-31	Compose pharmaceutique ou pesticide contenant du sulfoxyde de nitraminodiaryl
US4985463A (en)	1991-01-15	Aminodiaryl sulfoxide derivatives, process for their preparation and pharmaceutical and pesticidal compositions containing them
US5668172A (en)	1997-09-16	Anthraquinone pharmaceutical compounds and uses therefor
EP0135433B1 (fr)	1989-01-18	Dérivés de l'acide benzoique pour utilisation comme médicament et utilisation de ces dérivés comme agents conservateurs ou désinfectants
US4956007A (en)	1990-09-11	Nitraminodiaryl sulfoxide derivatives, process for their preparation and pharmaceutical and pesticidal compositions containing them
FI78460C (fi)	1989-08-10	Cykloalkanderivat, foerfarande foer deras framstaellning och kompositioner innehaollande dessa.
GB2118554A (en)	1983-11-02	N-carbamoyl derivatives of isothiazolo (5,4b)-pyridin-3-one
GB2155469A (en)	1985-09-25	Nitrodiaryl sulfoxide derivatives
US3715395A (en)	1973-02-06	Substituted thiobenzanilides
HU193531B (en)	1987-10-28	Process for preparing benzene-sulphonic acid derivatives and pharmaceutical compositions containing them
CA1230886A (fr)	1987-12-29	Procede de preparation de l'amidinouree et compose pharmaceutique le contenant
CA1247003A (fr)	1988-12-20	Derives d'aminodiaryl sulfoxyde, procede de preparation et composes pharmaceutiques et pesticides les contenant
FR2517202A1 (fr)	1983-06-03	Compositions pharmaceutiques presentant des proprietes normolipemiantes et contenant des composes ayant une structure du type benzenesulfonamides n-substitues
AU575132B2 (en)	1988-07-21	Preperation of amidinoureas
CA1266050A (fr)	1990-02-20	Procede de preparation de nouveaux derives de l'indole carboxamide et de leurs sels
US3395230A (en)	1968-07-30	Bis-phenyl thiocarbamate ester compositions
KR890004199B1 (ko)	1989-10-27	술포닐 우레아 유도체의 제조방법
IL43282A (en)	1976-07-30	N,n,n'-trimethyl-n'-(5-substituted-1,3,4-thiadiazol-2-yl)-ureas having selective herbicidal activity
HU196906B (en)	1989-02-28	Process for production of derivatives of new substituated diaryl-sulpholid and medical compositions containing these compounds as active substances
EP0526093A1 (fr)	1993-02-03	Médicaments non-stéroide comme inhibiteurs de 5-alpha réductase
JPS62195307A (ja)	1987-08-28	農園芸用殺菌剤
CH461509A (fr)	1968-08-31	Procédé de préparation de quinazolines
IE43858B1 (en)	1981-06-17	Phenylthionocarbomoyl alkylcarbaminate derivatives