NO750172L - - Google Patents

Info

Publication number: NO750172L
Authority: NO; Norway
Prior art keywords: trifluoromethyl; benzimidazole; animals; formula; integer
Prior art date: 1974-01-22

Application number

NO750172A

Other languages

English (en)

Norwegian (no)

Inventor

W Traber

E Aufderhaar

Original Assignee

Ciba Geigy Ag

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.)

1974-01-22

Filing date

1975-01-21

Publication date

1975-08-18

1975-01-21 Application filed by Ciba Geigy Ag filed Critical Ciba Geigy Ag

1975-08-18 Publication of NO750172L publication Critical patent/NO750172L/no

Links

239000000654 additive Substances 0.000 claims description 11
230000000996 additive effect Effects 0.000 claims description 7
229910052736 halogen Inorganic materials 0.000 claims description 7
150000002367 halogens Chemical class 0.000 claims description 7
MXFMPTXDHSDMTI-UHFFFAOYSA-N 2-(trifluoromethyl)-1h-benzimidazole Chemical class C1=CC=C2NC(C(F)(F)F)=NC2=C1 MXFMPTXDHSDMTI-UHFFFAOYSA-N 0.000 claims description 6
125000003342 alkenyl group Chemical group 0.000 claims description 6
125000000217 alkyl group Chemical group 0.000 claims description 5
150000001875 compounds Chemical class 0.000 claims description 5
244000000013 helminth Species 0.000 claims description 5
-1 haloalkyl radical Chemical class 0.000 claims description 4
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 3
125000003302 alkenyloxy group Chemical group 0.000 claims description 3
125000005136 alkenylsulfinyl group Chemical group 0.000 claims description 3
125000005108 alkenylthio group Chemical group 0.000 claims description 3
125000003545 alkoxy group Chemical group 0.000 claims description 3
125000004414 alkyl thio group Chemical group 0.000 claims description 3
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 3
150000007529 inorganic bases Chemical class 0.000 claims description 3
150000007530 organic bases Chemical class 0.000 claims description 3
229910052760 oxygen Inorganic materials 0.000 claims description 3
239000001301 oxygen Substances 0.000 claims description 3
150000003839 salts Chemical class 0.000 claims description 3
229910052717 sulfur Inorganic materials 0.000 claims description 3
239000011593 sulfur Substances 0.000 claims description 3
HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 claims description 2
125000005137 alkenylsulfonyl group Chemical group 0.000 claims description 2
125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 2
229910052740 iodine Inorganic materials 0.000 claims description 2
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QZWHWHNCPFEXLL-UHFFFAOYSA-N propan-2-yl n-[2-(1,3-thiazol-4-yl)-3h-benzimidazol-5-yl]carbamate Chemical compound N1C2=CC(NC(=O)OC(C)C)=CC=C2N=C1C1=CSC=N1 QZWHWHNCPFEXLL-UHFFFAOYSA-N 0.000 description 2
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IVFPIHZOFZLQJG-UHFFFAOYSA-N (5-methyl-2-propan-2-ylphenyl) n-(3-methylbutyl)carbamate Chemical compound CC(C)CCNC(=O)OC1=CC(C)=CC=C1C(C)C IVFPIHZOFZLQJG-UHFFFAOYSA-N 0.000 description 1
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IDIICHZCEIGXGB-UHFFFAOYSA-N 1-piperazinecarbodithioic acid Chemical compound SC(=S)N1CCNCC1 IDIICHZCEIGXGB-UHFFFAOYSA-N 0.000 description 1
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RPAJWWXZIQJVJF-UHFFFAOYSA-N 2,4-dichloro-6-(3,5-dichloro-2-hydroxyphenyl)sulfinylphenol Chemical compound OC1=C(Cl)C=C(Cl)C=C1S(=O)C1=CC(Cl)=CC(Cl)=C1O RPAJWWXZIQJVJF-UHFFFAOYSA-N 0.000 description 1
DWYHDSLIWMUSOO-UHFFFAOYSA-N 2-phenyl-1h-benzimidazole Chemical compound C1=CC=CC=C1C1=NC2=CC=CC=C2N1 DWYHDSLIWMUSOO-UHFFFAOYSA-N 0.000 description 1
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
AKPDNTFQNKKHSP-UHFFFAOYSA-N 4,6,7-trichloro-5-(3,4-dichlorophenoxy)-2-(trifluoromethyl)-1h-benzimidazole Chemical compound ClC=1C(Cl)=C2NC(C(F)(F)F)=NC2=C(Cl)C=1OC1=CC=C(Cl)C(Cl)=C1 AKPDNTFQNKKHSP-UHFFFAOYSA-N 0.000 description 1
ZSIQWWYOUYOECH-UHFFFAOYSA-N 4-bromo-5-methyl-2-propan-2-ylphenol Chemical compound CC(C)C1=CC(Br)=C(C)C=C1O ZSIQWWYOUYOECH-UHFFFAOYSA-N 0.000 description 1
WFJIVOKAWHGMBH-UHFFFAOYSA-N 4-hexylbenzene-1,3-diol Chemical compound CCCCCCC1=CC=C(O)C=C1O WFJIVOKAWHGMBH-UHFFFAOYSA-N 0.000 description 1
OUYBTFOUTJAWPZ-UHFFFAOYSA-N 4-iodo-5-methyl-2-propan-2-ylphenol Chemical compound CC(C)C1=CC(I)=C(C)C=C1O OUYBTFOUTJAWPZ-UHFFFAOYSA-N 0.000 description 1
NPTFBPRYLUYMJD-UHFFFAOYSA-N 4-phenylsulfanyl-2-(trifluoromethyl)-1h-benzimidazole Chemical class C=12NC(C(F)(F)F)=NC2=CC=CC=1SC1=CC=CC=C1 NPTFBPRYLUYMJD-UHFFFAOYSA-N 0.000 description 1
GLACISAPVWQBBO-UHFFFAOYSA-N 5-(4-bromophenoxy)-4,6,7-trichloro-2-(trifluoromethyl)-1h-benzimidazole Chemical compound ClC1=C2NC(C(F)(F)F)=NC2=C(Cl)C(Cl)=C1OC1=CC=C(Br)C=C1 GLACISAPVWQBBO-UHFFFAOYSA-N 0.000 description 1
ALJHHTHBYJROOG-UHFFFAOYSA-N 7-(dimethylamino)phenothiazin-3-one Chemical compound C1=CC(=O)C=C2SC3=CC(N(C)C)=CC=C3N=C21 ALJHHTHBYJROOG-UHFFFAOYSA-N 0.000 description 1
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MGYMHQJELJYRQS-UHFFFAOYSA-N Ascaridole Chemical compound C1CC2(C)OOC1(C(C)C)C=C2 MGYMHQJELJYRQS-UHFFFAOYSA-N 0.000 description 1
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235000012222 talc Nutrition 0.000 description 1
239000003784 tall oil Substances 0.000 description 1
WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 description 1
229960004546 thiabendazole Drugs 0.000 description 1
239000004308 thiabendazole Substances 0.000 description 1
235000010296 thiabendazole Nutrition 0.000 description 1
230000002110 toxicologic effect Effects 0.000 description 1
231100000723 toxicological property Toxicity 0.000 description 1
QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
239000011782 vitamin Substances 0.000 description 1
229940088594 vitamin Drugs 0.000 description 1
229930003231 vitamin Natural products 0.000 description 1
235000013343 vitamin Nutrition 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/06—Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
- C07D235/10—Radicals substituted by halogen atoms or nitro radicals

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Fodder In General (AREA)

NO750172A 1974-01-22 1975-01-21 NO750172L (nl)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH81974		1974-01-22

Publications (1)

Publication Number	Publication Date
NO750172L true NO750172L (nl)	1975-08-18

Family

ID=4195926

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO750172A NO750172L (nl)	1974-01-22	1975-01-21

Country Status (17)

Country	Link
US (1)	US3987181A (nl)
JP (1)	JPS50101512A (nl)
AU (1)	AU7747375A (nl)
BE (1)	BE824586A (nl)
DE (1)	DE2502116A1 (nl)
DK (1)	DK645374A (nl)
ES (1)	ES433982A1 (nl)
FI (1)	FI369174A (nl)
FR (1)	FR2258179B1 (nl)
GB (1)	GB1491742A (nl)
IE (1)	IE40363B1 (nl)
IL (1)	IL46473A (nl)
LU (1)	LU71694A1 (nl)
NL (1)	NL7500699A (nl)
NO (1)	NO750172L (nl)
SE (1)	SE7500571L (nl)
ZA (1)	ZA75392B (nl)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4205077A (en) *	1977-04-12	1980-05-27	Ciba-Geigy Corporation	Benzimidazole sulphides as anthelmintic agents
GB8426367D0 (en) *	1984-10-18	1984-11-21	Shell Int Research	Heteroaromatic ether herbicides
DE3621301A1 (de) *	1986-06-25	1988-01-07	Bayer Ag	2-trifluormethyl-benzimidazole
IE910278A1 (en) *	1990-02-16	1991-08-28	Ici Plc	Heterocyclic compounds
ATE402924T1 (de) *	2003-03-03	2008-08-15	Mycosol Inc	Pyridiniumsalze und deren verwendung
UA115981C2 (uk) *	2012-04-20	2018-01-25	Меріал, Інк.	Паразитицидні композиції, що містять похідні бензимідазолу, способи їх одержання та застосування

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3506767A (en) *	1965-08-06	1970-04-14	Geigy Chem Corp	Benzimidazole compositions and methods of use
US3749789A (en) *	1970-02-27	1973-07-31	Merck & Co Inc	Anthelmintic compositions containing benzimidazoles and method of use
US3749734A (en) *	1971-07-12	1973-07-31	Merck & Co Inc	1-cyanobenzimidazoles

1974
- 1974-12-11 DK DK645374A patent/DK645374A/da unknown
- 1974-12-19 FI FI3691/74A patent/FI369174A/fi unknown
1975
- 1975-01-17 US US05/541,980 patent/US3987181A/en not_active Expired - Lifetime
- 1975-01-20 GB GB2308/75A patent/GB1491742A/en not_active Expired
- 1975-01-20 DE DE19752502116 patent/DE2502116A1/de not_active Withdrawn
- 1975-01-20 SE SE7500571A patent/SE7500571L/xx unknown
- 1975-01-21 NL NL7500699A patent/NL7500699A/nl not_active Application Discontinuation
- 1975-01-21 JP JP50009219A patent/JPS50101512A/ja active Pending
- 1975-01-21 IL IL46473A patent/IL46473A/xx unknown
- 1975-01-21 FR FR7501759A patent/FR2258179B1/fr not_active Expired
- 1975-01-21 NO NO750172A patent/NO750172L/no unknown
- 1975-01-21 ES ES433982A patent/ES433982A1/es not_active Expired
- 1975-01-21 ZA ZA00750392A patent/ZA75392B/xx unknown
- 1975-01-21 BE BE152541A patent/BE824586A/xx unknown
- 1975-01-21 IE IE105/75A patent/IE40363B1/xx unknown
- 1975-01-21 LU LU71694*A patent/LU71694A1/xx unknown
- 1975-01-21 AU AU77473/75A patent/AU7747375A/en not_active Expired

Also Published As

Publication number	Publication date
FR2258179A1 (nl)	1975-08-18
NL7500699A (nl)	1975-07-24
ZA75392B (en)	1976-01-28
IE40363L (en)	1975-07-22
FI369174A (nl)	1975-07-23
IL46473A0 (en)	1975-04-25
IL46473A (en)	1978-07-31
ES433982A1 (es)	1976-11-16
LU71694A1 (nl)	1975-12-09
SE7500571L (nl)	1975-07-23
BE824586A (fr)	1975-07-22
GB1491742A (en)	1977-11-16
DK645374A (nl)	1975-09-29
DE2502116A1 (de)	1975-07-24
FR2258179B1 (nl)	1978-07-28
US3987181A (en)	1976-10-19
IE40363B1 (en)	1979-05-09
JPS50101512A (nl)	1975-08-12
AU7747375A (en)	1976-07-22

Publication	Publication Date	Title
FI56531C (fi)	1980-02-11	Foerfarande foer framstaellning av isotiocyanobenstiazoler med anthelmintisk och mikrobicid verkan
JP4163746B2 (ja)	2008-10-08	内部寄生虫を駆除するためのジオキソモルホリンの使用、新規ジオキソモルホリンおよびそれらの製造方法
JPH10511341A (ja)	1998-11-04	環状デプシペプチドのスルホニル化、スルフェニル化およびリン酸化の方法
NO750172L (nl)	1975-08-18
US3676561A (en)	1972-07-11	Anthelmintic compositions containing new carbamates and thiocarbamates and method of use
EP0230400A2 (de)	1987-07-29	N-3-(5-Trifluormethyl-pyridyl-2-oxy)-phenyl-N'-benzoylharnstoffe zur Bekämpfung von Helminthen an Nutztieren
DE2225071A1 (de)	1972-12-07	Verfahren zur Herstellung von heterocyclischen Verbindungen und deren Verwendung
US4151298A (en)	1979-04-24	Anthelmintic compositions
US3755406A (en)	1973-08-28	Isothiocyano diphenylamines
NZ210247A (en)	1988-01-08	Anthelmintic compositions containing levamisole derivatives
CN106061484B (zh)	2020-01-24	体内寄生虫防除剂
DE2016622A1 (en)	1971-10-21	Anthelmintic benzimidazole deriv
CH642359A5 (en)	1984-04-13	Benzimidazole derivatives
JPS5948420A (ja)	1984-03-19	駆虫剤
IE48383B1 (en)	1984-12-26	Benzothiazole derivatives anthelmintics
US3558784A (en)	1971-01-26	Anthelmintic compositions and methods of controlling parasitic helminths in animals
CN106029069B (zh)	2020-01-24	体内寄生虫防除剂
US3928437A (en)	1975-12-23	Phenoxy-phenyl, phenylthiophenyl, phenylsulfonylphenyl and phenylaminophenyl diaminothioureas
DE2800764A1 (de)	1978-07-13	Anthelmintika
US3968209A (en)	1976-07-06	Anthelmintic use of phosphorylated thioureas
CH507196A (de)	1971-05-15	Verfahren zur Herstellung neuer Isothiocyanato-diphenylamine
US3475444A (en)	1969-10-28	Complexes of 2-substituted benzimidazoles and bis-halogenated phenols
US3867535A (en)	1975-02-18	Thiadiazolium salts as antihelmintic agents
CA1217430A (en)	1987-02-03	Anthelmintics
DE2258279A1 (de)	1973-06-07	Kondensationsprodukte und ihre anwendung