IL119496A - Process for the preparation of dihaloazolopyrimidines and the corresponding diols - Google Patents

Process for the preparation of dihaloazolopyrimidines and the corresponding diols

Info

Publication number: IL119496A
Authority: IL; Israel
Prior art keywords: halogen; optionally substituted; cyano; nitro; process according
Prior art date: 1995-10-27

Application number

IL11949696A

Other languages

English (en)

Other versions

IL119496A0 (en

Original Assignee

American Home Prod

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.)

1995-10-27

Filing date

1996-10-27

Publication date

2001-07-24

1996-10-27 Application filed by American Home Prod filed Critical American Home Prod

1997-01-10 Publication of IL119496A0 publication Critical patent/IL119496A0/xx

2001-07-24 Publication of IL119496A publication Critical patent/IL119496A/en

Links

238000000034 method Methods 0.000 title claims abstract description 48
238000002360 preparation method Methods 0.000 title claims abstract description 21
150000002009 diols Chemical class 0.000 title description 2
229910052736 halogen Inorganic materials 0.000 claims abstract description 29
150000002367 halogens Chemical group 0.000 claims abstract description 29
125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 27
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 26
-1 malonic acid ester Chemical class 0.000 claims abstract description 24
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 21
150000003839 salts Chemical class 0.000 claims abstract description 17
239000001257 hydrogen Chemical group 0.000 claims abstract description 16
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 16
230000002140 halogenating effect Effects 0.000 claims abstract description 14
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims abstract description 12
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims abstract description 11
125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims abstract description 11
125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims abstract description 10
OFBLHCZYUXCKJZ-UHFFFAOYSA-N N1C(O)=NC(O)=C2N=CC=C21 Chemical compound N1C(O)=NC(O)=C2N=CC=C21 OFBLHCZYUXCKJZ-UHFFFAOYSA-N 0.000 claims abstract description 9
239000003795 chemical substances by application Substances 0.000 claims abstract description 9
239000011260 aqueous acid Substances 0.000 claims abstract description 8
150000001875 compounds Chemical class 0.000 claims abstract description 8
125000001624 naphthyl group Chemical group 0.000 claims abstract description 8
239000000460 chlorine Substances 0.000 claims abstract description 6
229910052801 chlorine Inorganic materials 0.000 claims abstract description 6
125000001309 chloro group Chemical group Cl* 0.000 claims abstract description 6
150000003512 tertiary amines Chemical class 0.000 claims abstract description 6
125000000882 C2-C6 alkenyl group Chemical group 0.000 claims abstract description 5
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims abstract description 4
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims abstract description 4
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims abstract description 4
229910052794 bromium Inorganic materials 0.000 claims abstract description 4
125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims abstract description 3
125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims abstract 6
125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims abstract 4
239000002904 solvent Substances 0.000 claims description 25
239000000203 mixture Substances 0.000 claims description 24
XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 claims description 18
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 16
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 15
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 13
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 12
125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 12
AUHZEENZYGFFBQ-UHFFFAOYSA-N mesitylene Substances CC1=CC(C)=CC(C)=C1 AUHZEENZYGFFBQ-UHFFFAOYSA-N 0.000 claims description 10
125000001827 mesitylenyl group Chemical group [H]C1=C(C(*)=C(C([H])=C1C([H])([H])[H])C([H])([H])[H])C([H])([H])[H] 0.000 claims description 10
SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical class N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 claims description 9
150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 9
238000009835 boiling Methods 0.000 claims description 8
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 8
239000002253 acid Substances 0.000 claims description 7
125000004429 atom Chemical group 0.000 claims description 7
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 6
125000001188 haloalkyl group Chemical group 0.000 claims description 5
OGFAWKRXZLGJSK-UHFFFAOYSA-N 1-(2,4-dihydroxyphenyl)-2-(4-nitrophenyl)ethanone Chemical compound OC1=CC(O)=CC=C1C(=O)CC1=CC=C([N+]([O-])=O)C=C1 OGFAWKRXZLGJSK-UHFFFAOYSA-N 0.000 claims description 4
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims description 4
UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims description 4
UXCDUFKZSUBXGM-UHFFFAOYSA-N phosphoric tribromide Chemical compound BrP(Br)(Br)=O UXCDUFKZSUBXGM-UHFFFAOYSA-N 0.000 claims description 4
UHZYTMXLRWXGPK-UHFFFAOYSA-N phosphorus pentachloride Chemical compound ClP(Cl)(Cl)(Cl)Cl UHZYTMXLRWXGPK-UHFFFAOYSA-N 0.000 claims description 4
BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 claims description 3
150000001412 amines Chemical class 0.000 claims description 3
125000003277 amino group Chemical group 0.000 claims description 3
229910052500 inorganic mineral Inorganic materials 0.000 claims description 3
239000011707 mineral Substances 0.000 claims description 3
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 3
239000008096 xylene Substances 0.000 claims description 3
125000003545 alkoxy group Chemical group 0.000 claims description 2
125000003118 aryl group Chemical group 0.000 claims description 2
150000003222 pyridines Chemical class 0.000 claims description 2
150000003248 quinolines Chemical class 0.000 claims description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims 2
125000004453 alkoxycarbonyl group Chemical group 0.000 claims 2
150000002148 esters Chemical class 0.000 claims 2
229920005547 polycyclic aromatic hydrocarbon Polymers 0.000 claims 2
239000004215 Carbon black (E152) Substances 0.000 claims 1
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
229930195733 hydrocarbon Natural products 0.000 claims 1
150000002430 hydrocarbons Chemical class 0.000 claims 1
150000002431 hydrogen Chemical group 0.000 abstract description 3
125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 2
125000006527 (C1-C5) alkyl group Chemical group 0.000 abstract 1
125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 1
125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 abstract 1
125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 1
239000002585 base Substances 0.000 description 18
239000000543 intermediate Substances 0.000 description 13
239000007787 solid Substances 0.000 description 10
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 9
238000006243 chemical reaction Methods 0.000 description 9
239000000047 product Substances 0.000 description 9
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
KLSJWNVTNUYHDU-UHFFFAOYSA-N Amitrole Chemical compound NC1=NC=NN1 KLSJWNVTNUYHDU-UHFFFAOYSA-N 0.000 description 5
CYTSAIIWPRPCIU-UHFFFAOYSA-N diethyl 2-(2-chloro-6-fluorophenyl)propanedioate Chemical compound CCOC(=O)C(C(=O)OCC)C1=C(F)C=CC=C1Cl CYTSAIIWPRPCIU-UHFFFAOYSA-N 0.000 description 5
QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 5
SNTWKPAKVQFCCF-UHFFFAOYSA-N 2,3-dihydro-1h-triazole Chemical compound N1NC=CN1 SNTWKPAKVQFCCF-UHFFFAOYSA-N 0.000 description 4
CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 4
235000011167 hydrochloric acid Nutrition 0.000 description 4
229960000443 hydrochloric acid Drugs 0.000 description 4
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
150000003230 pyrimidines Chemical class 0.000 description 3
239000011541 reaction mixture Substances 0.000 description 3
IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 3
LTMRRSWNXVJMBA-UHFFFAOYSA-L 2,2-diethylpropanedioate Chemical compound CCC(CC)(C([O-])=O)C([O-])=O LTMRRSWNXVJMBA-UHFFFAOYSA-L 0.000 description 2
JWYUFVNJZUSCSM-UHFFFAOYSA-N 2-aminobenzimidazole Chemical class C1=CC=C2NC(N)=NC2=C1 JWYUFVNJZUSCSM-UHFFFAOYSA-N 0.000 description 2
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 2
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 2
229910052784 alkaline earth metal Inorganic materials 0.000 description 2
238000005658 halogenation reaction Methods 0.000 description 2
238000005580 one pot reaction Methods 0.000 description 2
239000012074 organic phase Substances 0.000 description 2
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
239000002244 precipitate Substances 0.000 description 2
238000010992 reflux Methods 0.000 description 2
ZHCMLGWKJKQHTQ-UHFFFAOYSA-N 5,7-dichloro-2h-triazolo[4,5-d]pyrimidine Chemical compound N1=C(Cl)N=C(Cl)C2=NNN=C21 ZHCMLGWKJKQHTQ-UHFFFAOYSA-N 0.000 description 1
RVDLHGSZWAELAU-UHFFFAOYSA-N 5-tert-butylthiophene-2-carbonyl chloride Chemical compound CC(C)(C)C1=CC=C(C(Cl)=O)S1 RVDLHGSZWAELAU-UHFFFAOYSA-N 0.000 description 1
ZGUZCNWURZVWBJ-UHFFFAOYSA-N 6-(2-chloro-6-fluorophenyl)-7-hydroxy-1h-[1,2,4]triazolo[1,5-a]pyrimidin-5-one Chemical compound OC1=NC2=NC=NN2C(O)=C1C1=C(F)C=CC=C1Cl ZGUZCNWURZVWBJ-UHFFFAOYSA-N 0.000 description 1
KVGVQTOQSNJTJI-UHFFFAOYSA-N 8-azaxanthine Chemical compound O=C1NC(=O)NC2=C1NN=N2 KVGVQTOQSNJTJI-UHFFFAOYSA-N 0.000 description 1
RBMZETXPKBDNAD-UHFFFAOYSA-N C1(=CC(=CC(=C1)C)C)C.C(C)N(CC)CC Chemical compound C1(=CC(=CC(=C1)C)C)C.C(C)N(CC)CC RBMZETXPKBDNAD-UHFFFAOYSA-N 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
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 1
XUVKTNXVMHYRED-UHFFFAOYSA-M [OH-].[Na+].CC1=CC(C)=CC(C)=C1 Chemical compound [OH-].[Na+].CC1=CC(C)=CC(C)=C1 XUVKTNXVMHYRED-UHFFFAOYSA-M 0.000 description 1
229960000583 acetic acid Drugs 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
239000003905 agrochemical Substances 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
229910000288 alkali metal carbonate Inorganic materials 0.000 description 1
150000008041 alkali metal carbonates Chemical class 0.000 description 1
150000008044 alkali metal hydroxides Chemical class 0.000 description 1
150000001340 alkali metals Chemical class 0.000 description 1
229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 description 1
150000001342 alkaline earth metals Chemical class 0.000 description 1
229940111121 antirheumatic drug quinolines Drugs 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
244000309464 bull Species 0.000 description 1
229910000019 calcium carbonate Inorganic materials 0.000 description 1
AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
239000000920 calcium hydroxide Substances 0.000 description 1
229910001861 calcium hydroxide Inorganic materials 0.000 description 1
235000013877 carbamide Nutrition 0.000 description 1
239000002894 chemical waste Substances 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
238000006482 condensation reaction Methods 0.000 description 1
239000013078 crystal Substances 0.000 description 1
238000004821 distillation Methods 0.000 description 1
UKFXDFUAPNAMPJ-UHFFFAOYSA-N ethylmalonic acid Chemical compound CCC(C(O)=O)C(O)=O UKFXDFUAPNAMPJ-UHFFFAOYSA-N 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
230000000855 fungicidal effect Effects 0.000 description 1
239000012362 glacial acetic acid Substances 0.000 description 1
229940093915 gynecological organic acid Drugs 0.000 description 1
125000000623 heterocyclic group Chemical group 0.000 description 1
238000002955 isolation Methods 0.000 description 1
VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
239000000347 magnesium hydroxide Substances 0.000 description 1
229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
NTEUNCALHORCCY-UHFFFAOYSA-N n,n-diethylethanamine;toluene Chemical compound CCN(CC)CC.CC1=CC=CC=C1 NTEUNCALHORCCY-UHFFFAOYSA-N 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
QSLXBZBOAFVUQR-UHFFFAOYSA-N potassium 2-methylpropan-2-olate 1,3,5-trimethylbenzene Chemical compound [K+].CC(C)(C)[O-].Cc1cc(C)cc(C)c1 QSLXBZBOAFVUQR-UHFFFAOYSA-N 0.000 description 1
229910000027 potassium carbonate Inorganic materials 0.000 description 1
LPNYRYFBWFDTMA-UHFFFAOYSA-N potassium tert-butoxide Chemical compound [K+].CC(C)(C)[O-] LPNYRYFBWFDTMA-UHFFFAOYSA-N 0.000 description 1
239000011369 resultant mixture Substances 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
USSJTACOKOIINZ-UHFFFAOYSA-N sodium ethanolate 1,3,5-trimethylbenzene Chemical compound [Na+].CC[O-].Cc1cc(C)cc(C)c1 USSJTACOKOIINZ-UHFFFAOYSA-N 0.000 description 1
238000003756 stirring Methods 0.000 description 1
YWBFPKPWMSWWEA-UHFFFAOYSA-O triazolopyrimidine Chemical class BrC1=CC=CC(C=2N=C3N=CN[N+]3=C(NCC=3C=CN=CC=3)C=2)=C1 YWBFPKPWMSWWEA-UHFFFAOYSA-O 0.000 description 1
150000003672 ureas Chemical class 0.000 description 1
150000003738 xylenes Chemical class 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Nitrogen Condensed Heterocyclic Rings (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

IL11949696A 1995-10-27 1996-10-27 Process for the preparation of dihaloazolopyrimidines and the corresponding diols IL119496A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US802295P	1995-10-27	1995-10-27

Publications (2)

Publication Number	Publication Date
IL119496A0 IL119496A0 (en)	1997-01-10
IL119496A true IL119496A (en)	2001-07-24

Family

ID=21729405

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL11949696A IL119496A (en)	1995-10-27	1996-10-27	Process for the preparation of dihaloazolopyrimidines and the corresponding diols

Country Status (22)

Country	Link
US (1)	US5808066A (de)
EP (1)	EP0770615B1 (de)
JP (1)	JP4018182B2 (de)
KR (1)	KR100443182B1 (de)
AR (1)	AR004122A1 (de)
AT (1)	ATE243211T1 (de)
BR (1)	BR9605258A (de)
CA (1)	CA2188905C (de)
DE (1)	DE69628712T2 (de)
DK (1)	DK0770615T3 (de)
ES (1)	ES2202419T3 (de)
HU (1)	HU217773B (de)
IL (1)	IL119496A (de)
MX (1)	MX9604882A (de)
PT (1)	PT770615E (de)
RU (1)	RU2147584C1 (de)
SG (1)	SG55239A1 (de)
SI (1)	SI0770615T1 (de)
SK (1)	SK284071B6 (de)
TR (1)	TR199600792A2 (de)
UA (1)	UA48132C2 (de)
ZA (1)	ZA968957B (de)

Families Citing this family (40)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US6117876A (en)	1997-04-14	2000-09-12	American Cyanamid Company	Fungicidal trifluorophenyl-triazolopyrimidines
HUP0100885A3 (en) *	1998-02-11	2002-12-28	American Cyanamid Company Madi	Fungicidal 7-alkyl-triazolopyrimidines
US6117865A (en) *	1998-09-10	2000-09-12	American Cyanamid Company	Fungicidal trifluorophenyl-triazolopyrimidines
US6156925A (en) *	1998-09-25	2000-12-05	American Cyanamid Company	Process for the preparation of halogenated phenylmaloates
US6242451B1 (en) *	1998-09-25	2001-06-05	Klaus-Juergen Pees	Fungicidal trihalophenyl-triazolopyrimidines
US6380202B1 (en) *	1998-09-25	2002-04-30	Basf Aktiengesellschaft	Fungicidal fluoro-substituted 7-heterocyclyl-triazolopyrimidines
US6559151B2 (en)	2000-05-08	2003-05-06	Basf Aktiengesellschaft	6-(2-trifluoromethyl-phenyl)-triazolopyrimidines
US6756379B2 (en)	2001-07-26	2004-06-29	Taro Pharmaceutical Industries Ltd.	Non-sedating barbiturate compounds as neuroprotective agents
US7683071B2 (en) *	2000-07-26	2010-03-23	Taro Pharmaceuticals Industries Ltd.	Composition and method for improved bioavailability and enhanced brain delivery of 5,5-diphenyl barbituric acid
US6939873B2 (en) *	2000-07-26	2005-09-06	Taro Pharmaceuticals Industries Limited	Non-sedating barbituric acid derivatives
DE10063115A1 (de) *	2000-12-18	2002-06-27	Bayer Ag	Triazolopyrimidine
JP2002249492A (ja) *	2000-12-22	2002-09-06	Nippon Bayer Agrochem Co Ltd	トリアゾロピリミジン類
DE10121101A1 (de) *	2001-04-27	2002-10-31	Bayer Ag	Triazolopyrimidine
KR100619216B1 (ko)	2001-07-05	2006-09-08	바스프 악티엔게젤샤프트	살진균성 트리아졸로피리미딘, 이의 제조방법 및 유해진균 방제를 위한 이의 용도 및 상기 화합물을 포함하는조성물
US7038047B2 (en)	2001-07-18	2006-05-02	Basf Aktiengesellschaft	Substituted 6-(2-methoxyphenyl) triazolopyrimides as fungicides
HUP0401488A2 (hu)	2001-07-26	2004-12-28	Basf Aktiengesellschaft	Fungicid hatású 7-amino-triazolopirimidinek, előállításuk, alkalmazásuk és ilyeneket tartalmazó készítmények
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1996
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- 1996-10-16 DK DK96307528T patent/DK0770615T3/da active
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Publication number	Publication date
JP4018182B2 (ja)	2007-12-05
SK284071B6 (sk)	2004-09-08
SG55239A1 (en)	1998-12-21
HUP9602957A3 (en)	1998-01-28
KR970021081A (ko)	1997-05-28
ATE243211T1 (de)	2003-07-15
HU217773B (hu)	2000-04-28
US5808066A (en)	1998-09-15
SI0770615T1 (en)	2003-12-31
EP0770615B1 (de)	2003-06-18
JPH09124651A (ja)	1997-05-13
ZA968957B (en)	1998-04-24
SK137796A3 (en)	1997-05-07
DK0770615T3 (da)	2003-07-14
AR004122A1 (es)	1998-09-30
BR9605258A (pt)	1998-07-21
IL119496A0 (en)	1997-01-10
CA2188905C (en)	2005-12-06
TR199600792A2 (tr)	1997-05-21
EP0770615A1 (de)	1997-05-02
HU9602957D0 (en)	1996-12-30
UA48132C2 (uk)	2002-08-15
DE69628712D1 (de)	2003-07-24
KR100443182B1 (ko)	2005-04-19
PT770615E (pt)	2003-10-31
HUP9602957A2 (en)	1997-06-30
DE69628712T2 (de)	2004-04-29
ES2202419T3 (es)	2004-04-01
RU2147584C1 (ru)	2000-04-20
CA2188905A1 (en)	1997-04-28
MX9604882A (es)	1997-04-30

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KR102026059B1 (ko)	2019-09-26	치환된 5-플루오로-1h-피라졸로피리딘의 제조 방법
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