ZA200203861B

ZA200203861B - Pesticidal aminoheterocyclamide compounds.

Pesticidal aminoheterocyclamide compounds. Download PDF

Info

Publication number: ZA200203861B
Authority: ZA; South Africa
Prior art keywords: cfs; ccn; formula; alkyl; compounds
Prior art date: 1999-11-18

Application number

ZA200203861A

Other languages

English (en)

Inventor

Pierre Ducray

Jacques Bouvier

Urs Mueller

Original Assignee

Novartis Ag

Priority date

1999-11-18

Filing date

2002-05-15

Publication date

2002-12-05

2002-05-15 Application filed by Novartis Ag filed Critical Novartis Ag

2002-12-05 Publication of ZA200203861B publication Critical patent/ZA200203861B/en

Links

150000001875 compounds Chemical class 0.000 title claims description 93
230000000361 pesticidal effect Effects 0.000 title description 6
229910052739 hydrogen Inorganic materials 0.000 claims description 122
239000000203 mixture Substances 0.000 claims description 67
239000004480 active ingredient Substances 0.000 claims description 62
-1 penta-substituted phenyl Chemical group 0.000 claims description 41
241001465754 Metazoa Species 0.000 claims description 36
238000002360 preparation method Methods 0.000 claims description 24
238000000034 method Methods 0.000 claims description 23
239000001257 hydrogen Substances 0.000 claims description 22
125000001424 substituent group Chemical group 0.000 claims description 20
125000004432 carbon atom Chemical group C* 0.000 claims description 18
229910052736 halogen Inorganic materials 0.000 claims description 18
150000002367 halogens Chemical class 0.000 claims description 16
241000607479 Yersinia pestis Species 0.000 claims description 14
244000045947 parasite Species 0.000 claims description 14
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 12
229910052799 carbon Inorganic materials 0.000 claims description 10
150000002431 hydrogen Chemical class 0.000 claims description 10
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 10
230000008569 process Effects 0.000 claims description 10
239000000969 carrier Substances 0.000 claims description 9
125000004104 aryloxy group Chemical group 0.000 claims description 8
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 8
HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 claims description 5
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 3
125000004093 cyano group Chemical group *C#N 0.000 claims description 3
239000002270 dispersing agent Substances 0.000 claims description 3
239000003054 catalyst Substances 0.000 claims description 2
229910052757 nitrogen Inorganic materials 0.000 claims description 2
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OGHNVEJMJSYVRP-UHFFFAOYSA-N carvedilol Chemical compound COC1=CC=CC=C1OCCNCC(O)COC1=CC=CC2=C1C1=CC=CC=C1N2 OGHNVEJMJSYVRP-UHFFFAOYSA-N 0.000 claims 1
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