IL98743A - חומרי ביניים מתיל-2-)מתיל מותמר( -אלפא-אוקסובנזנאצטט עבור קוטלי פטריות - Google Patents
חומרי ביניים מתיל-2-)מתיל מותמר( -אלפא-אוקסובנזנאצטט עבור קוטלי פטריותInfo
- Publication number
- IL98743A IL98743A IL9874388A IL9874388A IL98743A IL 98743 A IL98743 A IL 98743A IL 9874388 A IL9874388 A IL 9874388A IL 9874388 A IL9874388 A IL 9874388A IL 98743 A IL98743 A IL 98743A
- Authority
- IL
- Israel
- Prior art keywords
- phenyl
- optionally substituted
- heteroaryl
- methyl
- compounds
- Prior art date
Links
- 239000000543 intermediate Substances 0.000 title description 4
- 239000000417 fungicide Substances 0.000 title description 3
- -1 Methyl 2-(substituted methyl)-alpha-oxobenzeneacetate Chemical class 0.000 title description 2
- 150000001875 compounds Chemical class 0.000 claims description 33
- 125000001072 heteroaryl group Chemical group 0.000 claims description 14
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 14
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 10
- 125000000217 alkyl group Chemical group 0.000 claims description 9
- 229910052757 nitrogen Inorganic materials 0.000 claims description 7
- 125000001424 substituent group Chemical group 0.000 claims description 5
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- 239000005864 Sulphur Substances 0.000 claims description 2
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 1
- 125000004627 thianthrenyl group Chemical group C1(=CC=CC=2SC3=CC=CC=C3SC12)* 0.000 claims 1
- 238000000034 method Methods 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 125000000468 ketone group Chemical group 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N Acrylic acid Chemical group OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- AMWRITDGCCNYAT-UHFFFAOYSA-L hydroxy(oxo)manganese;manganese Chemical compound [Mn].O[Mn]=O.O[Mn]=O AMWRITDGCCNYAT-UHFFFAOYSA-L 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- QBYIENPQHBMVBV-HFEGYEGKSA-N (2R)-2-hydroxy-2-phenylacetic acid Chemical class O[C@@H](C(O)=O)c1ccccc1.O[C@@H](C(O)=O)c1ccccc1 QBYIENPQHBMVBV-HFEGYEGKSA-N 0.000 description 1
- QEBYEVQKHRUYPE-UHFFFAOYSA-N 2-(2-chlorophenyl)-5-[(1-methylpyrazol-3-yl)methyl]-4-[[methyl(pyridin-3-ylmethyl)amino]methyl]-1h-pyrazolo[4,3-c]pyridine-3,6-dione Chemical compound C1=CN(C)N=C1CN1C(=O)C=C2NN(C=3C(=CC=CC=3)Cl)C(=O)C2=C1CN(C)CC1=CC=CN=C1 QEBYEVQKHRUYPE-UHFFFAOYSA-N 0.000 description 1
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000004230 Fast Yellow AB Substances 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
- 229930194542 Keto Natural products 0.000 description 1
- LOMVENUNSWAXEN-UHFFFAOYSA-N Methyl oxalate Chemical compound COC(=O)C(=O)OC LOMVENUNSWAXEN-UHFFFAOYSA-N 0.000 description 1
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000005213 alkyl heteroaryl group Chemical group 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 125000003784 fluoroethyl group Chemical group [H]C([H])(F)C([H])([H])* 0.000 description 1
- 125000005553 heteroaryloxy group Chemical group 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 125000005350 hydroxycycloalkyl group Chemical group 0.000 description 1
- 239000013461 intermediate chemical Substances 0.000 description 1
- 125000005647 linker group Chemical group 0.000 description 1
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 1
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical class [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 description 1
- 125000005704 oxymethylene group Chemical group [H]C([H])([*:2])O[*:1] 0.000 description 1
- WLJVXDMOQOGPHL-UHFFFAOYSA-N phenylacetic acid Chemical class OC(=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-UHFFFAOYSA-N 0.000 description 1
- 238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 1
- 229910052711 selenium Inorganic materials 0.000 description 1
- 239000011669 selenium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 125000000547 substituted alkyl group Chemical group 0.000 description 1
- CZDYPVPMEAXLPK-UHFFFAOYSA-N tetramethylsilane Chemical compound C[Si](C)(C)C CZDYPVPMEAXLPK-UHFFFAOYSA-N 0.000 description 1
- 238000000844 transformation Methods 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB878702845A GB8702845D0 (en) | 1987-02-09 | 1987-02-09 | Fungicides |
| GB878710594A GB8710594D0 (en) | 1987-05-05 | 1987-05-05 | Fungicides |
| IL8512288A IL85122A (he) | 1987-02-09 | 1988-01-19 | תולדות מתיל 2-]2-)1-אלק)נ(יל מותמר(פניל[-3- מתוקסיפרופנואט, הכנתן ותכשירים קוטלי פטריות המכיליםאותן |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| IL98743A true IL98743A (he) | 1996-10-16 |
Family
ID=27263311
Family Applications (5)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL107289A IL107289A (en) | 1987-02-09 | 1988-01-19 | METHYL a(o-SUBSTITUTED PHENYL)-b-METHOXY- ACRYLATE DERIVATIVES, THEIR PREPARATION AND FUNGICIDAL COMPOSITIONS CONTAINING THEM |
| IL9874388A IL98743A (he) | 1987-02-09 | 1988-01-19 | חומרי ביניים מתיל-2-)מתיל מותמר( -אלפא-אוקסובנזנאצטט עבור קוטלי פטריות |
| IL98741A IL98741A (en) | 1987-02-09 | 1988-01-19 | Methyl 3-methoxy-2- ((2-chloromethyl or formyl) phenyl) acrylates |
| IL9874288A IL98742A (he) | 1987-02-09 | 1988-01-19 | מתיל-2- )מתיל מותמר( -אלפא- )דימתוקסימתיל( -בנזנאצטט |
| IL107289A IL107289A0 (en) | 1987-02-09 | 1993-10-14 | Methyl a-phenylacrylate derivatives, their preparation and fungicidal compositions containing them |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL107289A IL107289A (en) | 1987-02-09 | 1988-01-19 | METHYL a(o-SUBSTITUTED PHENYL)-b-METHOXY- ACRYLATE DERIVATIVES, THEIR PREPARATION AND FUNGICIDAL COMPOSITIONS CONTAINING THEM |
Family Applications After (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL98741A IL98741A (en) | 1987-02-09 | 1988-01-19 | Methyl 3-methoxy-2- ((2-chloromethyl or formyl) phenyl) acrylates |
| IL9874288A IL98742A (he) | 1987-02-09 | 1988-01-19 | מתיל-2- )מתיל מותמר( -אלפא- )דימתוקסימתיל( -בנזנאצטט |
| IL107289A IL107289A0 (en) | 1987-02-09 | 1993-10-14 | Methyl a-phenylacrylate derivatives, their preparation and fungicidal compositions containing them |
Country Status (1)
| Country | Link |
|---|---|
| IL (5) | IL107289A (he) |
-
1988
- 1988-01-19 IL IL107289A patent/IL107289A/xx not_active IP Right Cessation
- 1988-01-19 IL IL9874388A patent/IL98743A/he not_active IP Right Cessation
- 1988-01-19 IL IL98741A patent/IL98741A/xx not_active IP Right Cessation
- 1988-01-19 IL IL9874288A patent/IL98742A/he not_active IP Right Cessation
-
1993
- 1993-10-14 IL IL107289A patent/IL107289A0/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| IL107289A0 (en) | 1994-01-25 |
| IL98741A (en) | 1993-03-15 |
| IL98742A (he) | 1996-06-18 |
| IL107289A (en) | 1997-06-10 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FF | Patent granted | ||
| KB | Patent renewed | ||
| KB | Patent renewed | ||
| KB | Patent renewed | ||
| HC | Change of name of proprietor(s) | ||
| KB | Patent renewed | ||
| EXP | Patent expired |