SK89996A3 - Aryl and heteroaryl pyrimidines and herbicidal agents containing them - Google Patents

Aryl and heteroaryl pyrimidines and herbicidal agents containing them Download PDF

Info

Publication number: SK89996A3
Authority: SK; Slovakia
Prior art keywords: group; optionally substituted; alkyl; phenyl; aryl
Prior art date: 1994-01-12

Application number

SK899-96A

Other languages

English (en)

Slovak (sk)

Inventor

John W Baum

Joe T Bamberg

Jonas A Grina

Original Assignee

Sandoz 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.)

1994-01-12

Filing date

1995-01-11

Publication date

1996-11-06

1995-01-11 Application filed by Sandoz Ag filed Critical Sandoz Ag

1996-11-06 Publication of SK89996A3 publication Critical patent/SK89996A3/sk

Links

-1 heteroaryl pyrimidines Chemical class 0.000 title claims abstract description 36
125000003118 aryl group Chemical group 0.000 title claims abstract description 6
239000004009 herbicide Substances 0.000 title abstract description 10
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 42
239000000203 mixture Substances 0.000 claims abstract description 20
125000000714 pyrimidinyl group Chemical group 0.000 claims abstract description 19
229910052717 sulfur Inorganic materials 0.000 claims abstract description 9
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract description 6
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 3
125000006615 aromatic heterocyclic group Chemical group 0.000 claims abstract description 3
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 3
229910052757 nitrogen Inorganic materials 0.000 claims abstract description 3
229910052760 oxygen Inorganic materials 0.000 claims abstract description 3
239000001301 oxygen Substances 0.000 claims abstract description 3
239000011593 sulfur Substances 0.000 claims abstract description 3
125000000217 alkyl group Chemical group 0.000 claims description 48
125000004432 carbon atom Chemical group C* 0.000 claims description 26
125000004076 pyridyl group Chemical group 0.000 claims description 20
125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 18
125000004183 alkoxy alkyl group Chemical group 0.000 claims description 17
125000003545 alkoxy group Chemical group 0.000 claims description 17
125000001188 haloalkyl group Chemical group 0.000 claims description 17
125000005843 halogen group Chemical group 0.000 claims description 17
125000003342 alkenyl group Chemical group 0.000 claims description 15
150000001768 cations Chemical class 0.000 claims description 15
125000001624 naphthyl group Chemical group 0.000 claims description 14
125000004591 piperonyl group Chemical group C(C1=CC=2OCOC2C=C1)* 0.000 claims description 14
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 13
230000002363 herbicidal effect Effects 0.000 claims description 13
229960005235 piperonyl butoxide Drugs 0.000 claims description 13
125000005493 quinolyl group Chemical group 0.000 claims description 13
125000001424 substituent group Chemical group 0.000 claims description 13
125000003884 phenylalkyl group Chemical group 0.000 claims description 11
125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 claims description 10
125000004541 benzoxazolyl group Chemical group O1C(=NC2=C1C=CC=C2)* 0.000 claims description 10
229910052739 hydrogen Inorganic materials 0.000 claims description 10
125000001041 indolyl group Chemical group 0.000 claims description 10
229910052736 halogen Inorganic materials 0.000 claims description 9
150000002367 halogens Chemical class 0.000 claims description 9
229910052708 sodium Inorganic materials 0.000 claims description 9
125000004663 dialkyl amino group Chemical group 0.000 claims description 8
125000005561 phenanthryl group Chemical group 0.000 claims description 8
229910052783 alkali metal Inorganic materials 0.000 claims description 7
229910052784 alkaline earth metal Inorganic materials 0.000 claims description 7
229910052791 calcium Inorganic materials 0.000 claims description 7
239000003085 diluting agent Substances 0.000 claims description 7
229910052749 magnesium Inorganic materials 0.000 claims description 7
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 7
125000004430 oxygen atom Chemical group O* 0.000 claims description 7
229910052700 potassium Inorganic materials 0.000 claims description 7
150000001340 alkali metals Chemical class 0.000 claims description 6
125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 6
125000003282 alkyl amino group Chemical group 0.000 claims description 6
125000004093 cyano group Chemical group *C#N 0.000 claims description 6
125000004438 haloalkoxy group Chemical group 0.000 claims description 6
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 6
KIWSYRHAAPLJFJ-DNZSEPECSA-N n-[(e,2z)-4-ethyl-2-hydroxyimino-5-nitrohex-3-enyl]pyridine-3-carboxamide Chemical compound [O-][N+](=O)C(C)C(/CC)=C/C(=N/O)/CNC(=O)C1=CC=CN=C1 KIWSYRHAAPLJFJ-DNZSEPECSA-N 0.000 claims description 6
XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical class [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 claims description 6
125000004434 sulfur atom Chemical group 0.000 claims description 6
NRZWQKGABZFFKE-UHFFFAOYSA-N trimethylsulfonium Chemical compound C[S+](C)C NRZWQKGABZFFKE-UHFFFAOYSA-N 0.000 claims description 6
YRYSAWZMIRQUBO-UHFFFAOYSA-N trimethylsulfoxonium Chemical compound C[S+](C)(C)=O YRYSAWZMIRQUBO-UHFFFAOYSA-N 0.000 claims description 6
125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 5
125000000304 alkynyl group Chemical group 0.000 claims description 5
239000001257 hydrogen Substances 0.000 claims description 5
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 5
125000005017 substituted alkenyl group Chemical group 0.000 claims description 5
125000000547 substituted alkyl group Chemical group 0.000 claims description 5
125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims description 4
125000002541 furyl group Chemical group 0.000 claims description 4
125000001072 heteroaryl group Chemical group 0.000 claims description 4
125000001786 isothiazolyl group Chemical group 0.000 claims description 4
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 4
125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims description 3
125000004414 alkyl thio group Chemical group 0.000 claims description 3
125000004644 alkyl sulfinyl group Chemical group 0.000 claims description 2
125000004429 atom Chemical group 0.000 claims description 2
125000002883 imidazolyl group Chemical group 0.000 claims description 2
125000005956 isoquinolyl group Chemical group 0.000 claims description 2
125000000842 isoxazolyl group Chemical group 0.000 claims description 2
125000001715 oxadiazolyl group Chemical group 0.000 claims description 2
125000002971 oxazolyl group Chemical group 0.000 claims description 2
125000003226 pyrazolyl group Chemical group 0.000 claims description 2
125000000168 pyrrolyl group Chemical group 0.000 claims description 2
125000002294 quinazolinyl group Chemical group N1=C(N=CC2=CC=CC=C12)* 0.000 claims description 2
125000001567 quinoxalinyl group Chemical group N1=C(C=NC2=CC=CC=C12)* 0.000 claims description 2
125000003107 substituted aryl group Chemical group 0.000 claims description 2
125000001113 thiadiazolyl group Chemical group 0.000 claims description 2
125000000335 thiazolyl group Chemical group 0.000 claims description 2
125000001544 thienyl group Chemical group 0.000 claims description 2
229940083082 pyrimidine derivative acting on arteriolar smooth muscle Drugs 0.000 abstract 1
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 75
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 57
239000011734 sodium Substances 0.000 description 40
150000001875 compounds Chemical class 0.000 description 38
239000007787 solid Substances 0.000 description 31
239000000243 solution Substances 0.000 description 24
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 21
WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 18
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 16
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 15
238000002360 preparation method Methods 0.000 description 15
241000196324 Embryophyta Species 0.000 description 14
229960003512 nicotinic acid Drugs 0.000 description 14
239000011664 nicotinic acid Substances 0.000 description 14
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
238000000354 decomposition reaction Methods 0.000 description 11
239000004480 active ingredient Substances 0.000 description 10
238000010992 reflux Methods 0.000 description 10
238000012360 testing method Methods 0.000 description 9
DDWXPXDQWQEBBY-UHFFFAOYSA-N methyl 2-[3-(dimethylamino)prop-2-enoyl]pyridine-3-carboxylate Chemical compound COC(=O)C1=CC=CN=C1C(=O)C=CN(C)C DDWXPXDQWQEBBY-UHFFFAOYSA-N 0.000 description 8
238000003828 vacuum filtration Methods 0.000 description 8
238000005160 1H NMR spectroscopy Methods 0.000 description 7
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
238000001819 mass spectrum Methods 0.000 description 5
238000000034 method Methods 0.000 description 5
230000001629 suppression Effects 0.000 description 5
239000004094 surface-active agent Substances 0.000 description 5
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
239000011575 calcium Substances 0.000 description 4
125000002768 hydroxyalkyl group Chemical group 0.000 description 4
239000011777 magnesium Substances 0.000 description 4
238000002844 melting Methods 0.000 description 4
230000008018 melting Effects 0.000 description 4
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
239000011541 reaction mixture Substances 0.000 description 4
238000003756 stirring Methods 0.000 description 4
239000000725 suspension Substances 0.000 description 4
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 3
239000002253 acid Substances 0.000 description 3
238000009472 formulation Methods 0.000 description 3
239000007788 liquid Substances 0.000 description 3
238000012986 modification Methods 0.000 description 3
230000004048 modification Effects 0.000 description 3
230000008635 plant growth Effects 0.000 description 3
239000000843 powder Substances 0.000 description 3
239000002244 precipitate Substances 0.000 description 3
238000010898 silica gel chromatography Methods 0.000 description 3
239000007921 spray Substances 0.000 description 3
238000005507 spraying Methods 0.000 description 3
239000004563 wettable powder Substances 0.000 description 3
KPPVNWGJXFMGAM-UUILKARUSA-N (e)-2-methyl-1-(6-methyl-3,4-dihydro-2h-quinolin-1-yl)but-2-en-1-one Chemical compound CC1=CC=C2N(C(=O)C(/C)=C/C)CCCC2=C1 KPPVNWGJXFMGAM-UUILKARUSA-N 0.000 description 2
125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 description 2
125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 description 2
239000005995 Aluminium silicate Substances 0.000 description 2
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
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 2
CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
208000027418 Wounds and injury Diseases 0.000 description 2
125000005078 alkoxycarbonylalkyl group Chemical group 0.000 description 2
235000012211 aluminium silicate Nutrition 0.000 description 2
150000001409 amidines Chemical class 0.000 description 2
230000033228 biological regulation Effects 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
239000013078 crystal Substances 0.000 description 2
230000006378 damage Effects 0.000 description 2
230000000694 effects Effects 0.000 description 2
239000004495 emulsifiable concentrate Substances 0.000 description 2
239000000706 filtrate Substances 0.000 description 2
239000008187 granular material Substances 0.000 description 2
208000014674 injury Diseases 0.000 description 2
230000000749 insecticidal effect Effects 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
238000004519 manufacturing process Methods 0.000 description 2
239000000463 material Substances 0.000 description 2
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 2
239000003094 microcapsule Substances 0.000 description 2
239000002245 particle Substances 0.000 description 2
230000000885 phytotoxic effect Effects 0.000 description 2
239000000047 product Substances 0.000 description 2
230000001105 regulatory effect Effects 0.000 description 2
229920005552 sodium lignosulfonate Polymers 0.000 description 2
239000011550 stock solution Substances 0.000 description 2
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
SZUVGFMDDVSKSI-WIFOCOSTSA-N (1s,2s,3s,5r)-1-(carboxymethyl)-3,5-bis[(4-phenoxyphenyl)methyl-propylcarbamoyl]cyclopentane-1,2-dicarboxylic acid Chemical compound O=C([C@@H]1[C@@H]([C@](CC(O)=O)([C@H](C(=O)N(CCC)CC=2C=CC(OC=3C=CC=CC=3)=CC=2)C1)C(O)=O)C(O)=O)N(CCC)CC(C=C1)=CC=C1OC1=CC=CC=C1 SZUVGFMDDVSKSI-WIFOCOSTSA-N 0.000 description 1
WWTBZEKOSBFBEM-SPWPXUSOSA-N (2s)-2-[[2-benzyl-3-[hydroxy-[(1r)-2-phenyl-1-(phenylmethoxycarbonylamino)ethyl]phosphoryl]propanoyl]amino]-3-(1h-indol-3-yl)propanoic acid Chemical compound N([C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)O)C(=O)C(CP(O)(=O)[C@H](CC=1C=CC=CC=1)NC(=O)OCC=1C=CC=CC=1)CC1=CC=CC=C1 WWTBZEKOSBFBEM-SPWPXUSOSA-N 0.000 description 1
125000006273 (C1-C3) alkyl group Chemical group 0.000 description 1
GDYXPZCCNRBQNS-VOTSOKGWSA-N (e)-3-phenylprop-2-enimidamide Chemical compound NC(=N)\C=C\C1=CC=CC=C1 GDYXPZCCNRBQNS-VOTSOKGWSA-N 0.000 description 1
ONBQEOIKXPHGMB-VBSBHUPXSA-N 1-[2-[(2s,3r,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-4,6-dihydroxyphenyl]-3-(4-hydroxyphenyl)propan-1-one Chemical compound O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1OC1=CC(O)=CC(O)=C1C(=O)CCC1=CC=C(O)C=C1 ONBQEOIKXPHGMB-VBSBHUPXSA-N 0.000 description 1
125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 description 1
AAILEWXSEQLMNI-UHFFFAOYSA-N 1h-pyridazin-6-one Chemical class OC1=CC=CN=N1 AAILEWXSEQLMNI-UHFFFAOYSA-N 0.000 description 1
CGNBQYFXGQHUQP-UHFFFAOYSA-N 2,3-dinitroaniline Chemical class NC1=CC=CC([N+]([O-])=O)=C1[N+]([O-])=O CGNBQYFXGQHUQP-UHFFFAOYSA-N 0.000 description 1
GQIZPSYLKHRSNS-UHFFFAOYSA-N 2-(3-chlorophenoxy)ethanimidamide Chemical compound NC(=N)COC1=CC=CC(Cl)=C1 GQIZPSYLKHRSNS-UHFFFAOYSA-N 0.000 description 1
JYUCDFZMJMRPHS-UHFFFAOYSA-N 2-acetylpyridine-3-carboxylic acid Chemical compound CC(=O)C1=NC=CC=C1C(O)=O JYUCDFZMJMRPHS-UHFFFAOYSA-N 0.000 description 1
YSUIQYOGTINQIN-UZFYAQMZSA-N 2-amino-9-[(1S,6R,8R,9S,10R,15R,17R,18R)-8-(6-aminopurin-9-yl)-9,18-difluoro-3,12-dihydroxy-3,12-bis(sulfanylidene)-2,4,7,11,13,16-hexaoxa-3lambda5,12lambda5-diphosphatricyclo[13.2.1.06,10]octadecan-17-yl]-1H-purin-6-one Chemical compound NC1=NC2=C(N=CN2[C@@H]2O[C@@H]3COP(S)(=O)O[C@@H]4[C@@H](COP(S)(=O)O[C@@H]2[C@@H]3F)O[C@H]([C@H]4F)N2C=NC3=C2N=CN=C3N)C(=O)N1 YSUIQYOGTINQIN-UZFYAQMZSA-N 0.000 description 1
TVTJUIAKQFIXCE-HUKYDQBMSA-N 2-amino-9-[(2R,3S,4S,5R)-4-fluoro-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-7-prop-2-ynyl-1H-purine-6,8-dione Chemical compound NC=1NC(C=2N(C(N(C=2N=1)[C@@H]1O[C@@H]([C@H]([C@H]1O)F)CO)=O)CC#C)=O TVTJUIAKQFIXCE-HUKYDQBMSA-N 0.000 description 1
JTQBLCCOULSWKX-UHFFFAOYSA-N 3-chloro-4-methylbenzenecarboximidamide Chemical compound CC1=CC=C(C(N)=N)C=C1Cl JTQBLCCOULSWKX-UHFFFAOYSA-N 0.000 description 1
KWDHABCUIIRLJP-UHFFFAOYSA-N 3-chlorobenzenecarboximidamide;hydrochloride Chemical compound Cl.NC(=N)C1=CC=CC(Cl)=C1 KWDHABCUIIRLJP-UHFFFAOYSA-N 0.000 description 1
OSTGTIZRQZOYAH-UHFFFAOYSA-N 4-fluorobenzenecarboximidamide Chemical compound NC(=N)C1=CC=C(F)C=C1 OSTGTIZRQZOYAH-UHFFFAOYSA-N 0.000 description 1
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
240000006995 Abutilon theophrasti Species 0.000 description 1
240000001592 Amaranthus caudatus Species 0.000 description 1
235000009328 Amaranthus caudatus Nutrition 0.000 description 1
244000237956 Amaranthus retroflexus Species 0.000 description 1
235000013479 Amaranthus retroflexus Nutrition 0.000 description 1
235000007320 Avena fatua Nutrition 0.000 description 1
241000209764 Avena fatua Species 0.000 description 1
244000075850 Avena orientalis Species 0.000 description 1
244000140786 Brassica hirta Species 0.000 description 1
241001148727 Bromus tectorum Species 0.000 description 1
125000004399 C1-C4 alkenyl group Chemical group 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
244000025254 Cannabis sativa Species 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
229920000742 Cotton Polymers 0.000 description 1
206010011878 Deafness Diseases 0.000 description 1
241000380130 Ehrharta erecta Species 0.000 description 1
IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 1
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
244000068988 Glycine max Species 0.000 description 1
235000010469 Glycine max Nutrition 0.000 description 1
244000060234 Gmelina philippensis Species 0.000 description 1
244000299507 Gossypium hirsutum Species 0.000 description 1
206010053759 Growth retardation Diseases 0.000 description 1
239000005909 Kieselgur Substances 0.000 description 1
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
ZSXGLVDWWRXATF-UHFFFAOYSA-N N,N-dimethylformamide dimethyl acetal Chemical compound COC(OC)N(C)C ZSXGLVDWWRXATF-UHFFFAOYSA-N 0.000 description 1
PVNIIMVLHYAWGP-UHFFFAOYSA-N Niacin Chemical class OC(=O)C1=CC=CN=C1 PVNIIMVLHYAWGP-UHFFFAOYSA-N 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
240000007594 Oryza sativa Species 0.000 description 1
235000007164 Oryza sativa Nutrition 0.000 description 1
244000088461 Panicum crus-galli Species 0.000 description 1
235000011999 Panicum crusgalli Nutrition 0.000 description 1
239000004372 Polyvinyl alcohol Substances 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
240000003461 Setaria viridis Species 0.000 description 1
235000002248 Setaria viridis Nutrition 0.000 description 1
KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical class [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
244000061457 Solanum nigrum Species 0.000 description 1
235000002594 Solanum nigrum Nutrition 0.000 description 1
235000021307 Triticum Nutrition 0.000 description 1
244000098338 Triticum aestivum Species 0.000 description 1
240000008042 Zea mays Species 0.000 description 1
235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
235000002017 Zea mays subsp mays Nutrition 0.000 description 1
241001148683 Zostera marina Species 0.000 description 1
BQVJCMMLDJPBFZ-UHFFFAOYSA-N [amino(phenyl)methylidene]azanium;chloride;hydrate Chemical compound O.Cl.NC(=N)C1=CC=CC=C1 BQVJCMMLDJPBFZ-UHFFFAOYSA-N 0.000 description 1
239000013543 active substance Substances 0.000 description 1
239000000654 additive Substances 0.000 description 1
150000001335 aliphatic alkanes Chemical class 0.000 description 1
235000012735 amaranth Nutrition 0.000 description 1
239000004178 amaranth Substances 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
150000003863 ammonium salts Chemical class 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
230000001147 anti-toxic effect Effects 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
239000003849 aromatic solvent Substances 0.000 description 1
238000003556 assay Methods 0.000 description 1
XRWSZZJLZRKHHD-WVWIJVSJSA-N asunaprevir Chemical compound O=C([C@@H]1C[C@H](CN1C(=O)[C@@H](NC(=O)OC(C)(C)C)C(C)(C)C)OC1=NC=C(C2=CC=C(Cl)C=C21)OC)N[C@]1(C(=O)NS(=O)(=O)C2CC2)C[C@H]1C=C XRWSZZJLZRKHHD-WVWIJVSJSA-N 0.000 description 1
JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 description 1
238000010533 azeotropic distillation Methods 0.000 description 1
229910052788 barium Inorganic materials 0.000 description 1
DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
239000002585 base Substances 0.000 description 1
235000010233 benzoic acid Nutrition 0.000 description 1
150000001559 benzoic acids Chemical class 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
235000011920 black pudding Nutrition 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
239000004490 capsule suspension Substances 0.000 description 1
150000004657 carbamic acid derivatives Chemical class 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
VXIVSQZSERGHQP-UHFFFAOYSA-N chloroacetamide Chemical class NC(=O)CCl VXIVSQZSERGHQP-UHFFFAOYSA-N 0.000 description 1
229940125904 compound 1 Drugs 0.000 description 1
229940126543 compound 14 Drugs 0.000 description 1
229940126142 compound 16 Drugs 0.000 description 1
229940126208 compound 22 Drugs 0.000 description 1
229940125961 compound 24 Drugs 0.000 description 1
229940125851 compound 27 Drugs 0.000 description 1
239000007859 condensation product Substances 0.000 description 1
235000005822 corn Nutrition 0.000 description 1
230000007797 corrosion Effects 0.000 description 1
238000005260 corrosion Methods 0.000 description 1
125000000753 cycloalkyl group Chemical group 0.000 description 1
WMPOZLHMGVKUEJ-UHFFFAOYSA-N decanedioyl dichloride Chemical compound ClC(=O)CCCCCCCCC(Cl)=O WMPOZLHMGVKUEJ-UHFFFAOYSA-N 0.000 description 1
230000035613 defoliation Effects 0.000 description 1
239000008367 deionised water Substances 0.000 description 1
229910021641 deionized water Inorganic materials 0.000 description 1
238000011161 development Methods 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
YDEXUEFDPVHGHE-GGMCWBHBSA-L disodium;(2r)-3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Na+].[Na+].COC1=CC=CC(C[C@H](CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O YDEXUEFDPVHGHE-GGMCWBHBSA-L 0.000 description 1
239000004491 dispersible concentrate Substances 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
238000009826 distribution Methods 0.000 description 1
MOTZDAYCYVMXPC-UHFFFAOYSA-N dodecyl hydrogen sulfate Chemical compound CCCCCCCCCCCCOS(O)(=O)=O MOTZDAYCYVMXPC-UHFFFAOYSA-N 0.000 description 1
238000001035 drying Methods 0.000 description 1
239000003480 eluent Substances 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
VJYFKVYYMZPMAB-UHFFFAOYSA-N ethoprophos Chemical compound CCCSP(=O)(OCC)SCCC VJYFKVYYMZPMAB-UHFFFAOYSA-N 0.000 description 1
239000002024 ethyl acetate extract Substances 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
238000001914 filtration Methods 0.000 description 1
229910052731 fluorine Inorganic materials 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
238000005187 foaming Methods 0.000 description 1
230000000855 fungicidal effect Effects 0.000 description 1
230000008570 general process Effects 0.000 description 1
230000012010 growth Effects 0.000 description 1
208000037824 growth disorder Diseases 0.000 description 1
231100000001 growth retardation Toxicity 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
238000010348 incorporation Methods 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
230000002401 inhibitory effect Effects 0.000 description 1
230000005764 inhibitory process Effects 0.000 description 1
239000011630 iodine Substances 0.000 description 1
229910052740 iodine Inorganic materials 0.000 description 1
JJWLVOIRVHMVIS-UHFFFAOYSA-O isopropylaminium Chemical compound CC(C)[NH3+] JJWLVOIRVHMVIS-UHFFFAOYSA-O 0.000 description 1
229920005610 lignin Polymers 0.000 description 1
229910052943 magnesium sulfate Inorganic materials 0.000 description 1
235000019341 magnesium sulphate Nutrition 0.000 description 1
238000004949 mass spectrometry Methods 0.000 description 1
COTNUBDHGSIOTA-UHFFFAOYSA-N meoh methanol Chemical compound OC.OC COTNUBDHGSIOTA-UHFFFAOYSA-N 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
150000002739 metals Chemical class 0.000 description 1
238000002156 mixing Methods 0.000 description 1
MELCHBVBYGSSOC-UHFFFAOYSA-N naphthalene-1-carboximidamide Chemical compound C1=CC=C2C(C(=N)N)=CC=CC2=C1 MELCHBVBYGSSOC-UHFFFAOYSA-N 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
230000000737 periodic effect Effects 0.000 description 1
230000000361 pesticidal effect Effects 0.000 description 1
239000000546 pharmaceutical excipient Substances 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
239000011591 potassium Substances 0.000 description 1
XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
230000008569 process Effects 0.000 description 1
235000009566 rice Nutrition 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
239000000741 silica gel Substances 0.000 description 1
229910002027 silica gel Inorganic materials 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
238000005245 sintering Methods 0.000 description 1
235000017557 sodium bicarbonate Nutrition 0.000 description 1
229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
235000019333 sodium laurylsulphate Nutrition 0.000 description 1
239000002689 soil Substances 0.000 description 1
239000012265 solid product Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
239000007858 starting material Substances 0.000 description 1
230000000638 stimulation Effects 0.000 description 1
229910052712 strontium Inorganic materials 0.000 description 1
CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
150000003558 thiocarbamic acid derivatives Chemical class 0.000 description 1
150000003918 triazines Chemical class 0.000 description 1
239000004562 water dispersible granule Substances 0.000 description 1
238000009736 wetting Methods 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
239000008096 xylene Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
- A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings

Landscapes

Organic Chemistry (AREA)
Chemical & Material Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Health & Medical Sciences (AREA)
Environmental Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Plant Pathology (AREA)
Pest Control & Pesticides (AREA)
Agronomy & Crop Science (AREA)
Plural Heterocyclic Compounds (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Pyridine Compounds (AREA)
Nitrogen Condensed Heterocyclic Rings (AREA)

SK899-96A 1994-01-12 1995-01-11 Aryl and heteroaryl pyrimidines and herbicidal agents containing them SK89996A3 (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US18025794A	1994-01-12	1994-01-12
PCT/EP1995/000086 WO1995019358A1 (en)	1994-01-12	1995-01-11	Herbicidal aryl and heteroaryl pyrimidines

Publications (1)

Publication Number	Publication Date
SK89996A3 true SK89996A3 (en)	1996-11-06

Family

ID=22659797

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SK899-96A SK89996A3 (en)	1994-01-12	1995-01-11	Aryl and heteroaryl pyrimidines and herbicidal agents containing them

Country Status (16)

Country	Link
EP (1)	EP0739341B1 (de)
JP (1)	JPH09508108A (de)
CN (1)	CN1044809C (de)
AT (1)	ATE180778T1 (de)
AU (1)	AU689532B2 (de)
BR (1)	BR9506482A (de)
CA (1)	CA2174730A1 (de)
CZ (1)	CZ205096A3 (de)
DE (1)	DE69510033T2 (de)
HU (1)	HUT74440A (de)
IL (1)	IL112290A (de)
MX (1)	MX9602493A (de)
PL (1)	PL314224A1 (de)
SK (1)	SK89996A3 (de)
WO (1)	WO1995019358A1 (de)
ZA (1)	ZA95221B (de)

Families Citing this family (23)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CO5210940A1 (es) *	1999-05-04	2002-10-30	Novartis Ag	Compuestos plaguicidas derivados de pirimidina y composiciones que los contienen
AR029489A1 (es)	2000-03-10	2003-07-02	Euro Celtique Sa	Piridinas, pirimidinas, pirazinas, triazinas sustituidas por arilo, composiciones farmaceuticas y el uso de las mismas para la manufactura de un medicamento
BR0109247A (pt)	2000-03-16	2002-12-17	Basf Ag	Processo para a preparação de 7-(pirazol-3-il) benzoxazóis, composto, uso de compostos, composição, e, processo para o combate de crescimento indesejado de planta
GB2361236B (en)	2000-03-29	2002-04-24	Cyclacel Ltd	Pyrimidines useful against proliferative disorders
DE60214701T2 (de)	2001-04-13	2007-09-13	Vertex Pharmaceuticals Inc., Cambridge	Inhibitoren von c-jun-n-terminalen-kinasen (jnk) und anderen proteinkinasen
AR037233A1 (es)	2001-09-07	2004-11-03	Euro Celtique Sa	Piridinas aril sustituidas, composiciones farmaceuticas y el uso de dichos compuestos para la elaboracion de un medicamento
AR036873A1 (es)	2001-09-07	2004-10-13	Euro Celtique Sa	Piridinas aril sustituidas a, composiciones farmaceuticas y el uso de las mismas para la preparacion de un medicamento
TWI329105B (en)	2002-02-01	2010-08-21	Rigel Pharmaceuticals Inc	2,4-pyrimidinediamine compounds and their uses
GB0215844D0 (en)	2002-07-09	2002-08-14	Novartis Ag	Organic compounds
IL166241A0 (en)	2002-07-29	2006-01-15	Rigel Pharmaceuticals Inc	Method of treating or preventing autoimmune diseases with 2,4-pyrimidinedinediamine compounds
ES2421139T3 (es)	2003-07-30	2013-08-29	Rigel Pharmaceuticals, Inc.	Compuestos de 2,4-pirimidindiamina para su uso en el tratamiento o la prevención de enfermedades autoinmunitarias
JP2007532669A (ja) *	2004-04-13	2007-11-15	イカジェンインコーポレイテッド	カリウムイオンチャネル調節剤としての多環式ピリミジン
JP4602686B2 (ja) *	2004-04-15	2010-12-22	広栄化学工業株式会社	２，６−ジハロゲノ−４−アリールピリジン類の製造法
CA2576159A1 (en)	2004-08-27	2006-03-02	Cyclacel Limited	Purine and pyrimidine cdk inhibitors and their use for the treatment of autoimmune diseases
JP2008515992A (ja) *	2004-10-13	2008-05-15	ピーティーシーセラピューティクス，インコーポレーテッド	体細胞変異に起因する疾患の阻止／治療用医薬を製造するための規定化合物の使用
ATE540035T1 (de)	2004-11-24	2012-01-15	Rigel Pharmaceuticals Inc	Spiro-2,4-pyrimidindiamin-verbindungen und ihre verwendungen
US7449458B2 (en)	2005-01-19	2008-11-11	Rigel Pharmaceuticals, Inc.	Prodrugs of 2,4-pyrimidinediamine compounds and their uses
CN102325736A (zh)	2009-01-09	2012-01-18	斯蒂芬·阿尔特	土工聚合物组合物
WO2014023670A1 (de) *	2012-08-07	2014-02-13	Bayer Cropscience Ag	Herbizid wirksame 6'-phenyl-2,2'-bipyridin-3-carbonsäure-derivate
US20150291553A1 (en) *	2012-08-07	2015-10-15	Bayer Cropscience Ag	Herbicidally active 2'-phenyl-2,4'-bipyridine-3-carboxylic acid derivatives
WO2014086738A1 (de) *	2012-12-06	2014-06-12	Bayer Cropscience Ag	Herbizid wirksame 4-amino-6-acyloxymethylpyrimidine und 4-amino-2-acyloxymethylpyridine
BR112017003745A2 (pt)	2014-08-29	2017-12-05	Tes Pharma S R L	inibidores de semialdeído descarboxilase de ácido alfa-amino-beta-carboximucônico
WO2018019552A1 (en) *	2016-07-25	2018-02-01	Basf Se	Herbicidal pyrimidine compounds

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3623302A1 (de) *	1985-11-09	1987-05-14	Bayer Ag	Nicotinsaeurederivate
DE4031798A1 (de) *	1990-10-08	1992-04-09	Hoechst Ag	Pyridylpyrimidine, verfahren zu ihrer herstellung, sie enthaltende mittel und ihre verwendung als fungizide
DE4035141A1 (de) *	1990-11-06	1992-05-07	Bayer Ag	Substituierte sulfonylaminotriazolylpyrimidine

1995
- 1995-01-10 IL IL11229095A patent/IL112290A/en not_active IP Right Cessation
- 1995-01-11 CA CA002174730A patent/CA2174730A1/en not_active Abandoned
- 1995-01-11 DE DE69510033T patent/DE69510033T2/de not_active Expired - Fee Related
- 1995-01-11 PL PL95314224A patent/PL314224A1/xx unknown
- 1995-01-11 AT AT95906329T patent/ATE180778T1/de active
- 1995-01-11 CN CN95191207A patent/CN1044809C/zh not_active Expired - Fee Related
- 1995-01-11 MX MX9602493A patent/MX9602493A/es unknown
- 1995-01-11 WO PCT/EP1995/000086 patent/WO1995019358A1/en not_active Ceased
- 1995-01-11 JP JP7518829A patent/JPH09508108A/ja active Pending
- 1995-01-11 AU AU14559/95A patent/AU689532B2/en not_active Ceased
- 1995-01-11 BR BR9506482A patent/BR9506482A/pt not_active Application Discontinuation
- 1995-01-11 EP EP95906329A patent/EP0739341B1/de not_active Expired - Lifetime
- 1995-01-11 CZ CZ962050A patent/CZ205096A3/cs unknown
- 1995-01-11 HU HU9601905A patent/HUT74440A/hu unknown
- 1995-01-11 SK SK899-96A patent/SK89996A3/sk unknown
- 1995-01-12 ZA ZA95221A patent/ZA95221B/xx unknown

Also Published As

Publication number	Publication date
HUT74440A (en)	1996-12-30
WO1995019358A1 (en)	1995-07-20
EP0739341B1 (de)	1999-06-02
AU1455995A (en)	1995-08-01
JPH09508108A (ja)	1997-08-19
MX9602493A (es)	1997-03-29
ATE180778T1 (de)	1999-06-15
IL112290A0 (en)	1995-03-30
EP0739341A1 (de)	1996-10-30
BR9506482A (pt)	1997-10-07
HU9601905D0 (en)	1996-09-30
PL314224A1 (en)	1996-09-02
DE69510033D1 (de)	1999-07-08
DE69510033T2 (de)	1999-10-28
CN1138859A (zh)	1996-12-25
CA2174730A1 (en)	1995-07-20
IL112290A (en)	1999-01-26
ZA95221B (en)	1996-07-12
CZ205096A3 (en)	1996-10-16
AU689532B2 (en)	1998-04-02
CN1044809C (zh)	1999-08-25

Publication	Publication Date	Title
EP0739341B1 (de)	1999-06-02	Aryl- und heteroaryl- pyrimidine als herbizide
LT3663B (en)	1996-01-25	Pyridine derivatives, process for their production, herbicidal method and composition
EP0184385A2 (de)	1986-06-11	N-[(4,6-Dimethoxypyrimidin-2-yl)aminocarbonyl]-3-trifluoromethylpyridin-2-sulfonamide oder Salze davon, diese enthaltendes herbizides Mittel und Verfahren zur Herstellung dieser Verbindung
JPH057385B2 (de)	1993-01-28
RU2066321C1 (ru)	1996-09-10	Производные пиридина или их соли, способ их получения, гербицидная композиция и способ уничтожения сорняков
CA1225399A (en)	1987-08-11	Carbamoyltriazoles, and their production and use
JPH05194492A (ja)	1993-08-03	除草剤及び植物成長制御剤としてのピリジルスルホニル尿素化合物の塩類、それらの製造及びそれらの利用方法
BG62051B1 (bg)	1999-01-29	Хербициден пиридинсулфонамид
US6124243A (en)	2000-09-26	Method of controlling graminaceous weeds
HU208230B (en)	1993-09-28	Herbicidal compositions comprising pyrimidine derivatives as active ingredient and process for producing the active ingredient and for using the composition
SK609586A3 (en)	1998-01-14	Semicarbazones and thiosemicarbazones
PL179601B1 (pl)	2000-09-29	Podstawiony zwiazek benzotriazolowy i kompozycja herbicydowa PL PL PL PL PL PL PL
US5863865A (en)	1999-01-26	Herbicidal 4-benzoylisoxazoles derivatives
US5139565A (en)	1992-08-18	Substituted pyridinesulfonamide compounds, and herbicidal compositions containing them
AU665818B2 (en)	1996-01-18	Novel arylindazoles and their use as herbicides
HU206592B (en)	1992-12-28	Herbicide and growth controlling compositions containing substituted sulfonyl-diamide derivatives as active components and process for producing the active components
AU603265B2 (en)	1990-11-08	Fungicidal pyridyl cyclopropane carboxamidines
JPS61236766A (ja)	1986-10-22	ｏ−置換フエノキシ複素環化合物、その製造法およびそれを有効成分とする除草剤
US6046136A (en)	2000-04-04	Herbicidal heterocyclic N-oxides compounds
US3999974A (en)	1976-12-28	Barbituric acid derivatives
US5536703A (en)	1996-07-16	Herbicidal substituted benzoyl bicycloalkanediones
JPH04226964A (ja)	1992-08-17	除草剤スルホニルウレア誘導体
DE3880988T2 (de)	1993-09-16	Cinnolin-derivate, verfahren zu deren herstellung und diese enthaltende herbizide zusammenstellungen.
US4927452A (en)	1990-05-22	1-carbonyl-2-pyrazoline derivatives having herbicidal activity
JP2997287B2 (ja)	2000-01-11	３―置換アルキルサリチレートを基礎としたフエノキシスルホニル尿素、それらの製造方法およびそれらの除草剤および植物生長調整剤としての使用方法