GB1140088A - Benzimidazole complexes - Google Patents
Benzimidazole complexesInfo
- Publication number
- GB1140088A GB1140088A GB19208/66A GB1920866A GB1140088A GB 1140088 A GB1140088 A GB 1140088A GB 19208/66 A GB19208/66 A GB 19208/66A GB 1920866 A GB1920866 A GB 1920866A GB 1140088 A GB1140088 A GB 1140088A
- Authority
- GB
- United Kingdom
- Prior art keywords
- ethyl
- dichloro
- furoate
- complexes
- acid
- 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.)
- Expired
Links
- 125000003785 benzimidazolyl group Chemical class N1=C(NC2=C1C=CC=C2)* 0.000 title 1
- 150000003839 salts Chemical class 0.000 abstract 4
- -1 halophenyl radical Chemical group 0.000 abstract 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical class [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 abstract 2
- 239000005864 Sulphur Substances 0.000 abstract 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 2
- 150000001556 benzimidazoles Chemical class 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001301 oxygen Substances 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- BNJMRELGMDUDDB-UHFFFAOYSA-N $l^{1}-sulfanylbenzene Chemical compound [S]C1=CC=CC=C1 BNJMRELGMDUDDB-UHFFFAOYSA-N 0.000 abstract 1
- YIWQMCDHLUECFK-UHFFFAOYSA-N 2,2,3,3-tetrachlorooxolane Chemical compound ClC1(Cl)CCOC1(Cl)Cl YIWQMCDHLUECFK-UHFFFAOYSA-N 0.000 abstract 1
- OFTKFKYVSBNYEC-UHFFFAOYSA-N 2-furoyl chloride Chemical compound ClC(=O)C1=CC=CO1 OFTKFKYVSBNYEC-UHFFFAOYSA-N 0.000 abstract 1
- UCQKVWANZGPZQF-UHFFFAOYSA-N 3,5-dichlorofuran-2-carboxylic acid Chemical compound OC(=O)C=1OC(Cl)=CC=1Cl UCQKVWANZGPZQF-UHFFFAOYSA-N 0.000 abstract 1
- VTLYSVKHSBKBNC-UHFFFAOYSA-N 4,5-dichlorofuran-2-carboxylic acid Chemical compound OC(=O)C1=CC(Cl)=C(Cl)O1 VTLYSVKHSBKBNC-UHFFFAOYSA-N 0.000 abstract 1
- BPYVAQCDJRTUHR-UHFFFAOYSA-N 4-chlorofuran-2-carboxylic acid Chemical compound OC(=O)C1=CC(Cl)=CO1 BPYVAQCDJRTUHR-UHFFFAOYSA-N 0.000 abstract 1
- LSJKFMKHHXFLSX-UHFFFAOYSA-N 5-nitro-2-phenylaniline Chemical group NC1=CC([N+]([O-])=O)=CC=C1C1=CC=CC=C1 LSJKFMKHHXFLSX-UHFFFAOYSA-N 0.000 abstract 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 abstract 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical class [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 abstract 1
- NHXSTXWKZVAVOQ-UHFFFAOYSA-N Ethyl furoate Chemical compound CCOC(=O)C1=CC=CO1 NHXSTXWKZVAVOQ-UHFFFAOYSA-N 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 abstract 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 abstract 1
- 229960000583 acetic acid Drugs 0.000 abstract 1
- 238000005904 alkaline hydrolysis reaction Methods 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000004414 alkyl thio group Chemical group 0.000 abstract 1
- 230000000507 anthelmentic effect Effects 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 229910052793 cadmium Inorganic materials 0.000 abstract 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 238000005660 chlorination reaction Methods 0.000 abstract 1
- 229910052804 chromium Inorganic materials 0.000 abstract 1
- 239000011651 chromium Substances 0.000 abstract 1
- 229910017052 cobalt Inorganic materials 0.000 abstract 1
- 239000010941 cobalt Substances 0.000 abstract 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 abstract 1
- 229910052802 copper Inorganic materials 0.000 abstract 1
- 239000010949 copper Substances 0.000 abstract 1
- VZCGXLVTQVOWKB-UHFFFAOYSA-N ethyl 2,3,4,5-tetrachlorooxolane-2-carboxylate Chemical compound CCOC(=O)C1(Cl)OC(Cl)C(Cl)C1Cl VZCGXLVTQVOWKB-UHFFFAOYSA-N 0.000 abstract 1
- VWHFBLQNEJUILB-UHFFFAOYSA-N ethyl 3,5-dichlorofuran-2-carboxylate Chemical compound C(C)OC(=O)C=1OC(=CC1Cl)Cl VWHFBLQNEJUILB-UHFFFAOYSA-N 0.000 abstract 1
- VSBLJUZVABUKOY-UHFFFAOYSA-N ethyl 4,5-dichlorofuran-2-carboxylate Chemical compound C(C)OC(=O)C=1OC(=C(C1)Cl)Cl VSBLJUZVABUKOY-UHFFFAOYSA-N 0.000 abstract 1
- CUBNSRFLRNKOBD-UHFFFAOYSA-N ethyl 5-chlorofuran-2-carboxylate Chemical compound CCOC(=O)C1=CC=C(Cl)O1 CUBNSRFLRNKOBD-UHFFFAOYSA-N 0.000 abstract 1
- 125000004494 ethyl ester group Chemical group 0.000 abstract 1
- 239000012362 glacial acetic acid Substances 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 125000005059 halophenyl group Chemical group 0.000 abstract 1
- 125000001072 heteroaryl group Chemical group 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 238000005984 hydrogenation reaction Methods 0.000 abstract 1
- 230000007062 hydrolysis Effects 0.000 abstract 1
- 238000006460 hydrolysis reaction Methods 0.000 abstract 1
- 229910052742 iron Chemical class 0.000 abstract 1
- 239000011133 lead Chemical class 0.000 abstract 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 abstract 1
- 229910052751 metal Inorganic materials 0.000 abstract 1
- 239000002184 metal Substances 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 229910052750 molybdenum Inorganic materials 0.000 abstract 1
- 239000011733 molybdenum Substances 0.000 abstract 1
- 229910052759 nickel Inorganic materials 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 238000007363 ring formation reaction Methods 0.000 abstract 1
- 125000001544 thienyl group Chemical group 0.000 abstract 1
- 239000011135 tin Substances 0.000 abstract 1
- 229910052718 tin Inorganic materials 0.000 abstract 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 abstract 1
- 229910052721 tungsten Inorganic materials 0.000 abstract 1
- 239000010937 tungsten Substances 0.000 abstract 1
- 229910052725 zinc Inorganic materials 0.000 abstract 1
- 239000011701 zinc Substances 0.000 abstract 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
- C07D235/18—Benzimidazoles; Hydrogenated benzimidazoles with aryl radicals directly attached in position 2
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US45381265A | 1965-05-06 | 1965-05-06 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1140088A true GB1140088A (en) | 1969-01-15 |
Family
ID=23802169
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB19208/66A Expired GB1140088A (en) | 1965-05-06 | 1966-05-02 | Benzimidazole complexes |
Country Status (7)
| Country | Link |
|---|---|
| BE (1) | BE680588A (enrdf_load_html_response) |
| BR (1) | BR6679256D0 (enrdf_load_html_response) |
| CH (1) | CH480349A (enrdf_load_html_response) |
| DE (1) | DE1620002A1 (enrdf_load_html_response) |
| ES (1) | ES326290A1 (enrdf_load_html_response) |
| GB (1) | GB1140088A (enrdf_load_html_response) |
| NL (1) | NL6606229A (enrdf_load_html_response) |
-
1966
- 1966-05-02 GB GB19208/66A patent/GB1140088A/en not_active Expired
- 1966-05-05 BR BR179256/66A patent/BR6679256D0/pt unknown
- 1966-05-05 CH CH651866A patent/CH480349A/de not_active IP Right Cessation
- 1966-05-05 DE DE19661620002 patent/DE1620002A1/de active Pending
- 1966-05-05 BE BE680588D patent/BE680588A/xx unknown
- 1966-05-06 NL NL6606229A patent/NL6606229A/xx unknown
- 1966-05-23 ES ES0326290A patent/ES326290A1/es not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| ES326290A1 (es) | 1967-03-01 |
| BE680588A (enrdf_load_html_response) | 1966-11-07 |
| DE1620002A1 (de) | 1970-03-12 |
| CH480349A (de) | 1969-10-31 |
| BR6679256D0 (pt) | 1973-09-04 |
| NL6606229A (enrdf_load_html_response) | 1966-11-07 |
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