IL37165A - Tetrazolo(1,5-a)quinoline agents for the control of plant-pathogenic organisms - Google Patents
Tetrazolo(1,5-a)quinoline agents for the control of plant-pathogenic organismsInfo
- Publication number
- IL37165A IL37165A IL37165A IL3716571A IL37165A IL 37165 A IL37165 A IL 37165A IL 37165 A IL37165 A IL 37165A IL 3716571 A IL3716571 A IL 3716571A IL 37165 A IL37165 A IL 37165A
- Authority
- IL
- Israel
- Prior art keywords
- quinoline
- compound
- composition
- formula
- compounds
- Prior art date
Links
- HHFCAUSIBNOUOP-UHFFFAOYSA-N tetrazolo[1,5-a]quinoline Chemical compound C1=CC2=NN=NN2C2=CC=CC=C21 HHFCAUSIBNOUOP-UHFFFAOYSA-N 0.000 title claims abstract description 7
- 239000000203 mixture Substances 0.000 claims abstract description 61
- 238000000034 method Methods 0.000 claims abstract description 46
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 claims description 145
- 150000001875 compounds Chemical class 0.000 claims description 139
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims description 43
- 239000001257 hydrogen Substances 0.000 claims description 34
- 229910052739 hydrogen Inorganic materials 0.000 claims description 34
- -1 cyano, hydroxy Chemical group 0.000 claims description 30
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 23
- 125000001424 substituent group Chemical group 0.000 claims description 22
- IOVCWXUNBOPUCH-UHFFFAOYSA-N Nitrous acid Chemical compound ON=O IOVCWXUNBOPUCH-UHFFFAOYSA-N 0.000 claims description 15
- 239000002253 acid Substances 0.000 claims description 15
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 14
- 150000002431 hydrogen Chemical class 0.000 claims description 13
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 13
- 239000007787 solid Substances 0.000 claims description 13
- 239000002270 dispersing agent Substances 0.000 claims description 11
- 244000000003 plant pathogen Species 0.000 claims description 11
- 238000002360 preparation method Methods 0.000 claims description 9
- 150000003839 salts Chemical class 0.000 claims description 8
- 125000003342 alkenyl group Chemical group 0.000 claims description 7
- 125000000304 alkynyl group Chemical group 0.000 claims description 5
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 5
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 5
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 5
- 239000011707 mineral Substances 0.000 claims description 5
- 241000233866 Fungi Species 0.000 claims description 4
- 125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 claims description 3
- 239000004480 active ingredient Substances 0.000 claims description 3
- 125000000852 azido group Chemical group *N=[N+]=[N-] 0.000 claims description 3
- 229910052736 halogen Inorganic materials 0.000 claims description 3
- 150000002367 halogens Chemical class 0.000 claims description 3
- 230000008569 process Effects 0.000 claims description 3
- DOOWXKYLEPTSIO-UHFFFAOYSA-N 5-methyltetrazolo[1,5-a]quinoline Chemical group C1=CC=C2C(C)=CC3=NN=NN3C2=C1 DOOWXKYLEPTSIO-UHFFFAOYSA-N 0.000 claims description 2
- XUTRWXRFMMTYCO-UHFFFAOYSA-N 9-chloro-4,5-dihydrotetrazolo[1,5-a]quinoline Chemical group ClC=1C=CC=C2CCC=3N(C12)N=NN3 XUTRWXRFMMTYCO-UHFFFAOYSA-N 0.000 claims description 2
- ACACVKXUSYYFOC-UHFFFAOYSA-N 9-chlorotetrazolo[1,5-a]quinoline Chemical group ClC=1C=CC=C2C=CC=3N(C12)N=NN3 ACACVKXUSYYFOC-UHFFFAOYSA-N 0.000 claims description 2
- YEYXCZTWSPNDQP-UHFFFAOYSA-N 9-methyltetrazolo[1,5-a]quinoline Chemical group CC=1C=CC=C2C=CC=3N(C12)N=NN3 YEYXCZTWSPNDQP-UHFFFAOYSA-N 0.000 claims description 2
- 230000002140 halogenating effect Effects 0.000 claims description 2
- 150000003248 quinolines Chemical class 0.000 claims description 2
- 239000013543 active substance Substances 0.000 claims 11
- 125000001475 halogen functional group Chemical group 0.000 claims 10
- XWABVGAOWUEUCD-UHFFFAOYSA-N 9-methyl-4,5-dihydrotetrazolo[1,5-a]quinoline Chemical compound CC=1C=CC=C2CCC=3N(C12)N=NN3 XWABVGAOWUEUCD-UHFFFAOYSA-N 0.000 claims 1
- 239000012677 causal agent Substances 0.000 claims 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims 1
- 230000002538 fungal effect Effects 0.000 abstract description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 51
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 36
- 241000196324 Embryophyta Species 0.000 description 35
- 239000000047 product Substances 0.000 description 33
- 239000000243 solution Substances 0.000 description 33
- 238000006243 chemical reaction Methods 0.000 description 30
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 28
- 241000209094 Oryza Species 0.000 description 25
- 235000007164 Oryza sativa Nutrition 0.000 description 25
- 235000009566 rice Nutrition 0.000 description 25
- 239000011541 reaction mixture Substances 0.000 description 23
- 201000010099 disease Diseases 0.000 description 21
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 21
- 238000012360 testing method Methods 0.000 description 16
- 238000011156 evaluation Methods 0.000 description 15
- 125000005843 halogen group Chemical group 0.000 description 15
- 239000007788 liquid Substances 0.000 description 15
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 13
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 12
- 239000002689 soil Substances 0.000 description 12
- 239000002904 solvent Substances 0.000 description 12
- 239000004576 sand Substances 0.000 description 11
- 238000004458 analytical method Methods 0.000 description 10
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 10
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 9
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 239000000725 suspension Substances 0.000 description 9
- 238000006722 reduction reaction Methods 0.000 description 7
- 239000007858 starting material Substances 0.000 description 7
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- 239000012141 concentrate Substances 0.000 description 6
- 239000000428 dust Substances 0.000 description 6
- 238000011065 in-situ storage Methods 0.000 description 6
- 230000009467 reduction Effects 0.000 description 6
- 235000010288 sodium nitrite Nutrition 0.000 description 6
- 239000007921 spray Substances 0.000 description 6
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 6
- 240000008067 Cucumis sativus Species 0.000 description 5
- 241000221785 Erysiphales Species 0.000 description 5
- 239000005457 ice water Substances 0.000 description 5
- 238000000926 separation method Methods 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 239000004094 surface-active agent Substances 0.000 description 5
- 235000010799 Cucumis sativus var sativus Nutrition 0.000 description 4
- PXIPVTKHYLBLMZ-UHFFFAOYSA-N Sodium azide Chemical compound [Na+].[N-]=[N+]=[N-] PXIPVTKHYLBLMZ-UHFFFAOYSA-N 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 150000007513 acids Chemical class 0.000 description 4
- 229910052783 alkali metal Inorganic materials 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- 239000007900 aqueous suspension Substances 0.000 description 4
- 230000001580 bacterial effect Effects 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
- 239000003995 emulsifying agent Substances 0.000 description 4
- 238000001914 filtration Methods 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- 238000010899 nucleation Methods 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- VLCMRTMCMQJSKM-UHFFFAOYSA-N phenyl-[4-phenyl-8-(trifluoromethyl)quinolin-3-yl]methanone Chemical compound C=1C=CC=CC=1C(=O)C1=CN=C2C(C(F)(F)F)=CC=CC2=C1C1=CC=CC=C1 VLCMRTMCMQJSKM-UHFFFAOYSA-N 0.000 description 4
- 238000000746 purification Methods 0.000 description 4
- LISFMEBWQUVKPJ-UHFFFAOYSA-N quinolin-2-ol Chemical compound C1=CC=C2NC(=O)C=CC2=C1 LISFMEBWQUVKPJ-UHFFFAOYSA-N 0.000 description 4
- 239000012429 reaction media Substances 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 208000024891 symptom Diseases 0.000 description 4
- 150000005635 2-haloquinolines Chemical class 0.000 description 3
- SZWPCUFXCNZZHY-UHFFFAOYSA-N 4,5-dihydrotetrazolo[1,5-a]quinoline Chemical compound C1CC2=CC=CC=C2N2C1=NN=N2 SZWPCUFXCNZZHY-UHFFFAOYSA-N 0.000 description 3
- RWGCICFWYGPRSW-UHFFFAOYSA-N 9-(ethoxymethyl)tetrazolo[1,5-a]quinoline Chemical compound C(C)OCC=1C=CC=C2C=CC=3N(C12)N=NN3 RWGCICFWYGPRSW-UHFFFAOYSA-N 0.000 description 3
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 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 3
- 206010061217 Infestation Diseases 0.000 description 3
- 241000227653 Lycopersicon Species 0.000 description 3
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 3
- 231100000674 Phytotoxicity Toxicity 0.000 description 3
- 241000918585 Pythium aphanidermatum Species 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000005984 hydrogenation reaction Methods 0.000 description 3
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 244000052769 pathogen Species 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- 229920006395 saturated elastomer Polymers 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 238000005507 spraying Methods 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical class OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 2
- ZNMGSDCIFYNPEK-UHFFFAOYSA-N 5-bromotetrazolo[1,5-a]quinoline Chemical compound BrC1=CC=2N(C3=CC=CC=C13)N=NN2 ZNMGSDCIFYNPEK-UHFFFAOYSA-N 0.000 description 2
- IRERXHZJMKGHII-UHFFFAOYSA-N 5-chlorotetrazolo[1,5-a]quinoline Chemical compound C1=CC=C2C(Cl)=CC3=NN=NN3C2=C1 IRERXHZJMKGHII-UHFFFAOYSA-N 0.000 description 2
- HZGKWCXXTAGNFC-UHFFFAOYSA-N 8-methyltetrazolo[1,5-a]quinoline Chemical compound C1=CC2=NN=NN2C2=CC(C)=CC=C21 HZGKWCXXTAGNFC-UHFFFAOYSA-N 0.000 description 2
- CVTZSIHAYZHHDZ-UHFFFAOYSA-N 9-(bromomethyl)tetrazolo[1,5-a]quinoline Chemical compound BrCC=1C=CC=C2C=CC=3N(C12)N=NN3 CVTZSIHAYZHHDZ-UHFFFAOYSA-N 0.000 description 2
- 229920001817 Agar Polymers 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 239000004342 Benzoyl peroxide Substances 0.000 description 2
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 241000222199 Colletotrichum Species 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- PCLIMKBDDGJMGD-UHFFFAOYSA-N N-bromosuccinimide Chemical compound BrN1C(=O)CCC1=O PCLIMKBDDGJMGD-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- 244000046052 Phaseolus vulgaris Species 0.000 description 2
- 206010034972 Photosensitivity reaction Diseases 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 239000008272 agar Substances 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- 150000001540 azides Chemical class 0.000 description 2
- 235000019400 benzoyl peroxide Nutrition 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 125000005745 ethoxymethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])* 0.000 description 2
- 239000000417 fungicide Substances 0.000 description 2
- 239000010440 gypsum Substances 0.000 description 2
- 229910052602 gypsum Inorganic materials 0.000 description 2
- 230000026030 halogenation Effects 0.000 description 2
- 238000005658 halogenation reaction Methods 0.000 description 2
- 239000004009 herbicide Substances 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 239000002917 insecticide Substances 0.000 description 2
- 229910052740 iodine Inorganic materials 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- MUMZUERVLWJKNR-UHFFFAOYSA-N oxoplatinum Chemical compound [Pt]=O MUMZUERVLWJKNR-UHFFFAOYSA-N 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 239000011574 phosphorus Substances 0.000 description 2
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 2
- 208000007578 phototoxic dermatitis Diseases 0.000 description 2
- 231100000018 phototoxicity Toxicity 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 229910003446 platinum oxide Inorganic materials 0.000 description 2
- 229910052903 pyrophyllite Inorganic materials 0.000 description 2
- 239000012258 stirred mixture Substances 0.000 description 2
- 238000010189 synthetic method Methods 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- NWZSZGALRFJKBT-KNIFDHDWSA-N (2s)-2,6-diaminohexanoic acid;(2s)-2-hydroxybutanedioic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O.NCCCC[C@H](N)C(O)=O NWZSZGALRFJKBT-KNIFDHDWSA-N 0.000 description 1
- PGGPUUOZTMQXOK-UHFFFAOYSA-N (6-chloro-3,4-dihydroquinolin-2-yl)hydrazine Chemical compound ClC=1C=C2CCC(=NC2=CC1)NN PGGPUUOZTMQXOK-UHFFFAOYSA-N 0.000 description 1
- PXDPUQZKEHNDAT-UHFFFAOYSA-N (6-methoxy-3,4-dihydroquinolin-2-yl)hydrazine Chemical compound N(N)C1=NC2=CC=C(C=C2CC1)OC PXDPUQZKEHNDAT-UHFFFAOYSA-N 0.000 description 1
- FILJMIULBHQKBA-UHFFFAOYSA-N (8-chloro-4-propyl-3,4-dihydroquinolin-2-yl)hydrazine Chemical compound ClC=1C=CC=C2C(CC(=NC12)NN)CCC FILJMIULBHQKBA-UHFFFAOYSA-N 0.000 description 1
- UJCPSHGLLVRPFC-UHFFFAOYSA-N 1,8-dimethylquinolin-2-one Chemical compound C1=CC(=O)N(C)C2=C1C=CC=C2C UJCPSHGLLVRPFC-UHFFFAOYSA-N 0.000 description 1
- NFNIRGPPIRJASP-UHFFFAOYSA-N 1-hydroxyquinolin-2-one Chemical compound C1=CC=C2C=CC(=O)N(O)C2=C1 NFNIRGPPIRJASP-UHFFFAOYSA-N 0.000 description 1
- KXZSVYHFYHTNBI-UHFFFAOYSA-N 1h-quinoline-2-thione Chemical compound C1=CC=CC2=NC(S)=CC=C21 KXZSVYHFYHTNBI-UHFFFAOYSA-N 0.000 description 1
- GAOXVBFIXYNMPI-UHFFFAOYSA-N 2-(tetrazolo[1,5-a]quinolin-9-yl)acetonitrile Chemical compound C(#N)CC=1C=CC=C2C=CC=3N(C12)N=NN3 GAOXVBFIXYNMPI-UHFFFAOYSA-N 0.000 description 1
- AQJPQJBGNLDISF-UHFFFAOYSA-N 2-chloro-6-ethyl-3-methylquinoline Chemical compound N1=C(Cl)C(C)=CC2=CC(CC)=CC=C21 AQJPQJBGNLDISF-UHFFFAOYSA-N 0.000 description 1
- ZLKRFLIUXVCYKM-UHFFFAOYSA-N 2-chloro-8-methylquinoline Chemical compound C1=C(Cl)N=C2C(C)=CC=CC2=C1 ZLKRFLIUXVCYKM-UHFFFAOYSA-N 0.000 description 1
- RVJHLZFALCBCIW-UHFFFAOYSA-N 2-chloro-8-nitroquinoline Chemical compound C1=C(Cl)N=C2C([N+](=O)[O-])=CC=CC2=C1 RVJHLZFALCBCIW-UHFFFAOYSA-N 0.000 description 1
- KIRRFWCTOASSJC-UHFFFAOYSA-N 2-hydrazinyl-3,4-dihydroquinoline-8-carbonitrile Chemical compound C(#N)C=1C=CC=C2CCC(=NC12)NN KIRRFWCTOASSJC-UHFFFAOYSA-N 0.000 description 1
- RQKYMHOXEANZSS-UHFFFAOYSA-N 3,4-dihydroquinolin-2-ylhydrazine Chemical compound C1=CC=C2CCC(NN)=NC2=C1 RQKYMHOXEANZSS-UHFFFAOYSA-N 0.000 description 1
- INUNLMUAPJVRME-UHFFFAOYSA-N 3-chloropropanoyl chloride Chemical compound ClCCC(Cl)=O INUNLMUAPJVRME-UHFFFAOYSA-N 0.000 description 1
- SJWMBVSZJUAJIC-UHFFFAOYSA-N 4,4-bis(methylsulfanyl)-1,3-dihydroquinolin-2-one Chemical compound CSC1(CC(NC2=CC=CC=C12)=O)SC SJWMBVSZJUAJIC-UHFFFAOYSA-N 0.000 description 1
- NLDOEEUPMLQTQN-UHFFFAOYSA-N 4,5-dichloro-4,5-dihydrotetrazolo[1,5-a]quinoline Chemical compound ClC1C=2N(C3=CC=CC=C3C1Cl)N=NN2 NLDOEEUPMLQTQN-UHFFFAOYSA-N 0.000 description 1
- QDYJUSLJEXSILA-UHFFFAOYSA-N 4,5-dichloro-9-methyl-4,5-dihydrotetrazolo[1,5-a]quinoline Chemical compound ClC1C=2N(C3=C(C=CC=C3C1Cl)C)N=NN2 QDYJUSLJEXSILA-UHFFFAOYSA-N 0.000 description 1
- BHQCQFFYRZLCQQ-UHFFFAOYSA-N 4-(3,7,12-trihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1h-cyclopenta[a]phenanthren-17-yl)pentanoic acid Chemical compound OC1CC2CC(O)CCC2(C)C2C1C1CCC(C(CCC(O)=O)C)C1(C)C(O)C2 BHQCQFFYRZLCQQ-UHFFFAOYSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 1
- PSYDZPWQNCTPSH-UHFFFAOYSA-N 5,9-dichloro-4-methyltetrazolo[1,5-a]quinoline Chemical compound ClC1=C(C=2N(C3=C(C=CC=C13)Cl)N=NN2)C PSYDZPWQNCTPSH-UHFFFAOYSA-N 0.000 description 1
- IHKARKYCSPNCOE-UHFFFAOYSA-N 5,9-dichlorotetrazolo[1,5-a]quinoline Chemical compound ClC1=CC=2N(C3=C(C=CC=C13)Cl)N=NN2 IHKARKYCSPNCOE-UHFFFAOYSA-N 0.000 description 1
- NPCHHUUAEKZDSK-UHFFFAOYSA-N 5-(bromomethyl)tetrazolo[1,5-a]quinoline Chemical compound BrCC1=CC=2N(C3=CC=CC=C13)N=NN2 NPCHHUUAEKZDSK-UHFFFAOYSA-N 0.000 description 1
- OERVOMUQLSLUBJ-UHFFFAOYSA-N 5-(methoxymethyl)tetrazolo[1,5-a]quinoline Chemical compound COCC1=CC=2N(C3=CC=CC=C13)N=NN2 OERVOMUQLSLUBJ-UHFFFAOYSA-N 0.000 description 1
- IJJWOSAXNHWBPR-HUBLWGQQSA-N 5-[(3as,4s,6ar)-2-oxo-1,3,3a,4,6,6a-hexahydrothieno[3,4-d]imidazol-4-yl]-n-(6-hydrazinyl-6-oxohexyl)pentanamide Chemical compound N1C(=O)N[C@@H]2[C@H](CCCCC(=O)NCCCCCC(=O)NN)SC[C@@H]21 IJJWOSAXNHWBPR-HUBLWGQQSA-N 0.000 description 1
- CBGANACUFGKQRG-UHFFFAOYSA-N 5-azidotetrazolo[1,5-a]quinoline tetrazolo[1,5-a]quinolin-5-ylmethanamine Chemical compound N(=[N+]=[N-])C1=CC=2N(C3=CC=CC=C13)N=NN2.NCC2=CC=1N(C3=CC=CC=C23)N=NN1 CBGANACUFGKQRG-UHFFFAOYSA-N 0.000 description 1
- CVICEEPAFUYBJG-UHFFFAOYSA-N 5-chloro-2,2-difluoro-1,3-benzodioxole Chemical group C1=C(Cl)C=C2OC(F)(F)OC2=C1 CVICEEPAFUYBJG-UHFFFAOYSA-N 0.000 description 1
- VBVXRCQOTWKASO-UHFFFAOYSA-N 5-chloro-4-ethyltetrazolo[1,5-a]quinoline Chemical compound ClC1=C(C=2N(C3=CC=CC=C13)N=NN2)CC VBVXRCQOTWKASO-UHFFFAOYSA-N 0.000 description 1
- LNGHFHMHVPZAEI-UHFFFAOYSA-N 5-chloro-9-methyltetrazolo[1,5-a]quinoline Chemical compound ClC1=CC=2N(C3=C(C=CC=C13)C)N=NN2 LNGHFHMHVPZAEI-UHFFFAOYSA-N 0.000 description 1
- ZSVKFKXNDGRUCT-UHFFFAOYSA-N 7-chlorotetrazolo[1,5-a]quinoline Chemical compound C1=CC2=NN=NN2C2=CC=C(Cl)C=C12 ZSVKFKXNDGRUCT-UHFFFAOYSA-N 0.000 description 1
- KPCZNAJNCBVEGO-UHFFFAOYSA-N 7-methoxy-4,5-dihydrotetrazolo[1,5-a]quinoline Chemical compound C1CC2=NN=NN2C2=CC=C(OC)C=C12 KPCZNAJNCBVEGO-UHFFFAOYSA-N 0.000 description 1
- XDALRUCOJSFQHF-UHFFFAOYSA-N 8-chloro-4-propylsulfanyl-3,4-dihydro-1H-quinolin-2-one Chemical compound ClC=1C=CC=C2C(CC(NC=12)=O)SCCC XDALRUCOJSFQHF-UHFFFAOYSA-N 0.000 description 1
- SLZBGODISVKKIX-UHFFFAOYSA-N 8-methylsulfanyl-3,4-dihydro-1H-quinolin-2-one Chemical compound CSC=1C=CC=C2CCC(NC=12)=O SLZBGODISVKKIX-UHFFFAOYSA-N 0.000 description 1
- JVGSXUOUBVUFTP-UHFFFAOYSA-N 9-bromo-5-methyltetrazolo[1,5-a]quinoline Chemical compound BrC=1C=CC=C2C(=CC=3N(C12)N=NN3)C JVGSXUOUBVUFTP-UHFFFAOYSA-N 0.000 description 1
- BIGHANSBJYNBRZ-UHFFFAOYSA-N 9-chloro-5-propyl-4,5-dihydrotetrazolo[1,5-a]quinoline Chemical compound ClC=1C=CC=C2C(CC=3N(C12)N=NN3)CCC BIGHANSBJYNBRZ-UHFFFAOYSA-N 0.000 description 1
- RJMDSCFHYUDRHS-UHFFFAOYSA-N 9-ethyl-5-methyltetrazolo[1,5-a]quinoline Chemical compound C(C)C=1C=CC=C2C(=CC=3N(C12)N=NN3)C RJMDSCFHYUDRHS-UHFFFAOYSA-N 0.000 description 1
- 241000589158 Agrobacterium Species 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 1
- IVRMZWNICZWHMI-UHFFFAOYSA-N Azide Chemical compound [N-]=[N+]=[N-] IVRMZWNICZWHMI-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- WLIYFQKEQQQJMC-UHFFFAOYSA-N N-(tetrazolo[1,5-a]quinolin-9-yl)acetamide Chemical compound C(C)(=O)NC=1C=CC=C2C=CC=3N(C12)N=NN3 WLIYFQKEQQQJMC-UHFFFAOYSA-N 0.000 description 1
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N N-phenyl amine Natural products NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 1
- LDUMKMVPKVZZMU-UHFFFAOYSA-N N1=NN=C2N1C1=CC=CC=C1C=C2.N2=CC=CC1=CC=CC=C21 Chemical compound N1=NN=C2N1C1=CC=CC=C1C=C2.N2=CC=CC1=CC=CC=C21 LDUMKMVPKVZZMU-UHFFFAOYSA-N 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 101100313649 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) POT1 gene Proteins 0.000 description 1
- 206010039509 Scab Diseases 0.000 description 1
- 241001061127 Thione Species 0.000 description 1
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 1
- 208000027418 Wounds and injury Diseases 0.000 description 1
- 101100161758 Yarrowia lipolytica (strain CLIB 122 / E 150) POX3 gene Proteins 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- AZFNGPAYDKGCRB-XCPIVNJJSA-M [(1s,2s)-2-amino-1,2-diphenylethyl]-(4-methylphenyl)sulfonylazanide;chlororuthenium(1+);1-methyl-4-propan-2-ylbenzene Chemical compound [Ru+]Cl.CC(C)C1=CC=C(C)C=C1.C1=CC(C)=CC=C1S(=O)(=O)[N-][C@@H](C=1C=CC=CC=1)[C@@H](N)C1=CC=CC=C1 AZFNGPAYDKGCRB-XCPIVNJJSA-M 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 238000005273 aeration Methods 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 230000009435 amidation Effects 0.000 description 1
- 238000007112 amidation reaction Methods 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- 150000001448 anilines Chemical class 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 229960000892 attapulgite Drugs 0.000 description 1
- 230000003190 augmentative effect Effects 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 125000001246 bromo group Chemical group Br* 0.000 description 1
- 125000005997 bromomethyl group Chemical group 0.000 description 1
- 244000309464 bull Species 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000009903 catalytic hydrogenation reaction Methods 0.000 description 1
- 238000010531 catalytic reduction reaction Methods 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 238000012258 culturing Methods 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 230000003292 diminished effect Effects 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 235000021186 dishes Nutrition 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000000921 elemental analysis Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 239000012458 free base Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- IKDUDTNKRLTJSI-UHFFFAOYSA-N hydrazine monohydrate Substances O.NN IKDUDTNKRLTJSI-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- JUINSXZKUKVTMD-UHFFFAOYSA-N hydrogen azide Chemical compound N=[N+]=[N-] JUINSXZKUKVTMD-UHFFFAOYSA-N 0.000 description 1
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 238000007373 indentation Methods 0.000 description 1
- 208000014674 injury Diseases 0.000 description 1
- 238000011081 inoculation Methods 0.000 description 1
- 239000002054 inoculum Substances 0.000 description 1
- 239000011872 intimate mixture Substances 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 150000002828 nitro derivatives Chemical class 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 231100001085 no phototoxicity Toxicity 0.000 description 1
- 229910000510 noble metal Inorganic materials 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 238000005580 one pot reaction Methods 0.000 description 1
- 235000015205 orange juice Nutrition 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 230000001717 pathogenic effect Effects 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000003209 petroleum derivative Substances 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 1
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 1
- TZLVRPLSVNESQC-UHFFFAOYSA-N potassium azide Chemical compound [K+].[N-]=[N+]=[N-] TZLVRPLSVNESQC-UHFFFAOYSA-N 0.000 description 1
- 239000004304 potassium nitrite Substances 0.000 description 1
- 235000010289 potassium nitrite Nutrition 0.000 description 1
- 239000001965 potato dextrose agar Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 230000002062 proliferating effect Effects 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000008223 sterile water Substances 0.000 description 1
- 239000002352 surface water Substances 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- 239000012085 test solution Substances 0.000 description 1
- XUCMFFGAWNYTTO-UHFFFAOYSA-N tetrazolo[1,5-a]quinolin-5-ylmethanamine Chemical compound NCC1=CC=2N(C3=CC=CC=C13)N=NN2 XUCMFFGAWNYTTO-UHFFFAOYSA-N 0.000 description 1
- OWUKCZZTRFFUAS-UHFFFAOYSA-N tetrazolo[1,5-a]quinolin-5-ylmethanol Chemical compound OCC1=CC=2N(C3=CC=CC=C13)N=NN2 OWUKCZZTRFFUAS-UHFFFAOYSA-N 0.000 description 1
- FCFDMVSXGPYNPJ-UHFFFAOYSA-N tetrazolo[1,5-a]quinolin-9-amine Chemical compound NC=1C=CC=C2C=CC=3N(C12)N=NN3 FCFDMVSXGPYNPJ-UHFFFAOYSA-N 0.000 description 1
- 231100000167 toxic agent Toxicity 0.000 description 1
- 239000003440 toxic substance Substances 0.000 description 1
- 229940086542 triethylamine Drugs 0.000 description 1
- 238000007039 two-step reaction Methods 0.000 description 1
- 239000010455 vermiculite Substances 0.000 description 1
- 229910052902 vermiculite Inorganic materials 0.000 description 1
- 235000019354 vermiculite Nutrition 0.000 description 1
- 230000003612 virological effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D215/38—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D215/18—Halogen atoms or nitro radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D215/48—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Quinoline Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US5332070A | 1970-07-08 | 1970-07-08 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| IL37165A true IL37165A (en) | 1977-05-31 |
Family
ID=21983402
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL37165A IL37165A (en) | 1970-07-08 | 1971-06-27 | Tetrazolo(1,5-a)quinoline agents for the control of plant-pathogenic organisms |
Country Status (26)
| Country | Link |
|---|---|
| US (1) | US3764681A (da) |
| JP (4) | JPS5328487B1 (da) |
| KR (1) | KR780000450B1 (da) |
| AR (1) | AR194342A1 (da) |
| AT (2) | AT321641B (da) |
| BE (1) | BE769600A (da) |
| BG (2) | BG18867A3 (da) |
| CA (1) | CA995221A (da) |
| CH (1) | CH554637A (da) |
| DE (2) | DE2134146C3 (da) |
| DK (1) | DK139069B (da) |
| ES (2) | ES392993A1 (da) |
| FR (1) | FR2098255B1 (da) |
| GB (2) | GB1327311A (da) |
| HU (1) | HU163863B (da) |
| IE (1) | IE35416B1 (da) |
| IL (1) | IL37165A (da) |
| MY (2) | MY7500263A (da) |
| NL (1) | NL156575B (da) |
| PH (1) | PH10293A (da) |
| PL (3) | PL90713B1 (da) |
| SE (2) | SE372691B (da) |
| SU (2) | SU649293A3 (da) |
| TR (1) | TR18087A (da) |
| YU (1) | YU36027B (da) |
| ZA (1) | ZA714210B (da) |
Families Citing this family (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3953457A (en) * | 1972-07-28 | 1976-04-27 | Eli Lilly And Company | Agent for the control of plant-pathogenic organisms |
| US3907993A (en) * | 1974-03-14 | 1975-09-23 | Dow Chemical Co | Method for systemically controlling plant disease employing certain pyridazines |
| US3911127A (en) * | 1974-03-14 | 1975-10-07 | Dow Chemical Co | Systemic plant protectant methods employing certain pyridazines |
| US3974286A (en) * | 1975-02-07 | 1976-08-10 | Eli Lilly And Company | S-Triazolo [5,1-b]benzothiazoles as fungicidal agents |
| US3988455A (en) * | 1975-06-10 | 1976-10-26 | Eli Lilly And Company | Ditetrazolo(1,5-a:5',1'-c)quinoxalines for control of soil-borne phytopathogens |
| US4008322A (en) * | 1975-06-10 | 1977-02-15 | Eli Lilly And Company | Triazolo(4,3-a)quinoxalines for control of rice |
| US3987196A (en) * | 1975-06-10 | 1976-10-19 | Eli Lilly And Company | Tetrazolo(1,5-a)quinoxalines for control of phytopathogens |
| US4001227A (en) * | 1975-12-22 | 1977-01-04 | Eli Lilly And Company | Tetrazolo- and triazolobenzothiazines |
| DE3210979A1 (de) * | 1982-03-25 | 1983-09-29 | Basf Ag, 6700 Ludwigshafen | 3-chlor-8-cyano-chinoline, verfahren zu ihrer herstellung und ihre verwendung zur bekaempfung unerwuenschten pflanzenwuchses |
| US4496569A (en) * | 1983-03-25 | 1985-01-29 | The Dow Chemical Company | Antiallergic (1H-tetrazol-5-yl)tetrazolo[1,5-a]quinolines and derivatives thereof |
| US5153196A (en) * | 1991-06-05 | 1992-10-06 | Eli Lilly And Company | Excitatory amino acid receptor antagonists and methods for the use thereof |
| US5196421A (en) * | 1991-06-05 | 1993-03-23 | Eli Lilly And Company | Excitatory amino acid receptor antagonists in methods for the use thereof |
| ES2120185T3 (es) * | 1994-03-25 | 1998-10-16 | Merrell Pharma Inc | Procedimiento para preparar (1h-tetrazol-5-il)tetrazolo(1,5-a)quinolinas y naftiridinas. |
| US5693811A (en) * | 1996-06-21 | 1997-12-02 | Minnesota Mining And Manufacturing Company | Process for preparing tetrahdroimidazoquinolinamines |
| US5741908A (en) | 1996-06-21 | 1998-04-21 | Minnesota Mining And Manufacturing Company | Process for reparing imidazoquinolinamines |
| UA67760C2 (uk) * | 1997-12-11 | 2004-07-15 | Міннесота Майнінг Енд Мануфакчурінг Компані | Імідазонафтиридин та тетрагідроімідазонафтиридин, фармацевтична композиція, спосіб індукування біосинтезу цитокінів та спосіб лікування вірусної інфекції, проміжні сполуки |
| US8436176B2 (en) * | 2004-12-30 | 2013-05-07 | Medicis Pharmaceutical Corporation | Process for preparing 2-methyl-1-(2-methylpropyl)-1H-imidazo[4,5-c][1,5]naphthyridin-4-amine |
| AU2006223148A1 (en) * | 2005-03-14 | 2006-09-21 | 3M Innovative Properties Company | Method of treating actinic keratosis |
| DE102009007038A1 (de) | 2009-02-02 | 2010-08-05 | Merck Patent Gmbh | Metallkomplexe |
| CN116444527A (zh) * | 2023-03-30 | 2023-07-18 | 中国工程物理研究院化工材料研究所 | 一种稠合三环骨架的高效构筑方法及其含能衍生物的合成方法 |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1251327B (de) * | 1964-10-26 | 1967-10-05 | Eastman Kodak Company, Rochester, NY (V St A) | Verfahren zur Her Stellung von in 5 Stellung substituierten 1 Aryl-lH-tetrazolen |
| US3389137A (en) * | 1965-08-03 | 1968-06-18 | American Cyanamid Co | Heterocyclic phosphine imide compounds and preparation |
-
1970
- 1970-07-08 US US00053320A patent/US3764681A/en not_active Expired - Lifetime
-
1971
- 1971-06-27 IL IL37165A patent/IL37165A/en unknown
- 1971-06-28 ZA ZA714210A patent/ZA714210B/xx unknown
- 1971-06-29 CA CA116,943A patent/CA995221A/en not_active Expired
- 1971-06-30 IE IE839/71A patent/IE35416B1/xx unknown
- 1971-07-02 YU YU1756/71A patent/YU36027B/xx unknown
- 1971-07-05 GB GB3134171A patent/GB1327311A/en not_active Expired
- 1971-07-05 GB GB2711772A patent/GB1327312A/en not_active Expired
- 1971-07-05 SE SE7108670A patent/SE372691B/xx unknown
- 1971-07-06 PH PH12603A patent/PH10293A/en unknown
- 1971-07-06 JP JP4986871A patent/JPS5328487B1/ja active Pending
- 1971-07-06 TR TR18087A patent/TR18087A/xx unknown
- 1971-07-07 DK DK334571AA patent/DK139069B/da not_active IP Right Cessation
- 1971-07-07 PL PL1971176328A patent/PL90713B1/pl unknown
- 1971-07-07 ES ES392993A patent/ES392993A1/es not_active Expired
- 1971-07-07 PL PL1971156555A patent/PL89008B1/pl unknown
- 1971-07-07 HU HUEI380A patent/HU163863B/hu unknown
- 1971-07-07 KR KR7102340A patent/KR780000450B1/ko active
- 1971-07-07 PL PL1971149272A patent/PL81817B1/pl unknown
- 1971-07-07 BE BE769600A patent/BE769600A/xx not_active IP Right Cessation
- 1971-07-08 NL NL7109476.A patent/NL156575B/xx not_active IP Right Cessation
- 1971-07-08 SU SU711685174A patent/SU649293A3/ru active
- 1971-07-08 DE DE2134146A patent/DE2134146C3/de not_active Expired
- 1971-07-08 AT AT595871A patent/AT321641B/de not_active IP Right Cessation
- 1971-07-08 AT AT859572A patent/AT326662B/de not_active IP Right Cessation
- 1971-07-08 DE DE2166398A patent/DE2166398C3/de not_active Expired
- 1971-07-08 BG BG18020A patent/BG18867A3/xx unknown
- 1971-07-08 FR FR7125106A patent/FR2098255B1/fr not_active Expired
- 1971-07-08 BG BG7100022531A patent/BG25438A1/xx unknown
- 1971-07-08 AR AR236681A patent/AR194342A1/es active
- 1971-07-08 CH CH1006871A patent/CH554637A/xx not_active IP Right Cessation
-
1972
- 1972-05-26 SU SU721788406A patent/SU648103A3/ru active
-
1974
- 1974-04-30 ES ES425853A patent/ES425853A1/es not_active Expired
- 1974-07-30 SE SE7409801A patent/SE422061B/xx unknown
-
1975
- 1975-12-30 MY MY263/75A patent/MY7500263A/xx unknown
- 1975-12-30 MY MY262/75A patent/MY7500262A/xx unknown
-
1976
- 1976-10-08 JP JP51121162A patent/JPS5257194A/ja active Granted
- 1976-10-08 JP JP51121163A patent/JPS5257195A/ja active Granted
- 1976-10-08 JP JP51121161A patent/JPS5257322A/ja active Granted
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