AR126248A1 - Un proceso para la preparación de diamidas antranílicas bicíclicas de fórmula (i) e intermediarios de las mismas - Google Patents
Un proceso para la preparación de diamidas antranílicas bicíclicas de fórmula (i) e intermediarios de las mismasInfo
- Publication number
- AR126248A1 AR126248A1 ARP220101674A ARP220101674A AR126248A1 AR 126248 A1 AR126248 A1 AR 126248A1 AR P220101674 A ARP220101674 A AR P220101674A AR P220101674 A ARP220101674 A AR P220101674A AR 126248 A1 AR126248 A1 AR 126248A1
- Authority
- AR
- Argentina
- Prior art keywords
- formula
- salt
- compound
- group
- alkyl
- Prior art date
Links
- 238000000034 method Methods 0.000 title abstract 4
- 150000001470 diamides Chemical class 0.000 title abstract 3
- 150000003839 salts Chemical class 0.000 abstract 38
- 150000001875 compounds Chemical class 0.000 abstract 32
- 239000002904 solvent Substances 0.000 abstract 10
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 8
- 229910052739 hydrogen Inorganic materials 0.000 abstract 8
- 239000001257 hydrogen Substances 0.000 abstract 8
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 6
- 239000003153 chemical reaction reagent Substances 0.000 abstract 6
- 229910052736 halogen Inorganic materials 0.000 abstract 5
- 150000002367 halogens Chemical class 0.000 abstract 5
- 150000002431 hydrogen Chemical group 0.000 abstract 5
- WEVYAHXRMPXWCK-UHFFFAOYSA-N methyl cyanide Natural products CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 abstract 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 5
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 abstract 4
- 230000003301 hydrolyzing effect Effects 0.000 abstract 4
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 3
- -1 1H-pyrazol-1-yl Chemical class 0.000 abstract 3
- 229940059260 amidate Drugs 0.000 abstract 3
- 150000001412 amines Chemical class 0.000 abstract 3
- 230000008878 coupling Effects 0.000 abstract 3
- 238000010168 coupling process Methods 0.000 abstract 3
- 238000005859 coupling reaction Methods 0.000 abstract 3
- NPUKDXXFDDZOKR-LLVKDONJSA-N etomidate Chemical compound CCOC(=O)C1=CN=CN1[C@H](C)C1=CC=CC=C1 NPUKDXXFDDZOKR-LLVKDONJSA-N 0.000 abstract 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- 125000002619 bicyclic group Chemical group 0.000 abstract 2
- ITVPBBDAZKBMRP-UHFFFAOYSA-N chloro-dioxido-oxo-$l^{5}-phosphane;hydron Chemical compound OP(O)(Cl)=O ITVPBBDAZKBMRP-UHFFFAOYSA-N 0.000 abstract 2
- 238000004519 manufacturing process Methods 0.000 abstract 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 2
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 1
- ZJGSHCNIWOBHOH-UHFFFAOYSA-N 1-cyanoethylphosphonic acid Chemical class N#CC(C)P(O)(O)=O ZJGSHCNIWOBHOH-UHFFFAOYSA-N 0.000 abstract 1
- ZYVYEJXMYBUCMN-UHFFFAOYSA-N 1-methoxy-2-methylpropane Chemical compound COCC(C)C ZYVYEJXMYBUCMN-UHFFFAOYSA-N 0.000 abstract 1
- 125000004793 2,2,2-trifluoroethoxy group Chemical group FC(CO*)(F)F 0.000 abstract 1
- KWMBADTWRIGGGG-UHFFFAOYSA-N 2-diethoxyphosphorylacetonitrile Chemical compound CCOP(=O)(CC#N)OCC KWMBADTWRIGGGG-UHFFFAOYSA-N 0.000 abstract 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 1
- JNCMHMUGTWEVOZ-UHFFFAOYSA-N F[CH]F Chemical group F[CH]F JNCMHMUGTWEVOZ-UHFFFAOYSA-N 0.000 abstract 1
- 108010081348 HRT1 protein Hairy Chemical group 0.000 abstract 1
- 102100021881 Hairy/enhancer-of-split related with YRPW motif protein 1 Human genes 0.000 abstract 1
- VDIKHHGNSVEWPF-UHFFFAOYSA-N OC(=O)CN1N=CC=C1C=O Chemical class OC(=O)CN1N=CC=C1C=O VDIKHHGNSVEWPF-UHFFFAOYSA-N 0.000 abstract 1
- 150000007960 acetonitrile Chemical class 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- 125000005347 halocycloalkyl group Chemical group 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 239000013067 intermediate product Substances 0.000 abstract 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 abstract 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 abstract 1
Classifications
-
- 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)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Plural Heterocyclic Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IN202111028885 | 2021-06-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR126248A1 true AR126248A1 (es) | 2023-10-04 |
Family
ID=82703044
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP220101674A AR126248A1 (es) | 2021-06-28 | 2022-06-27 | Un proceso para la preparación de diamidas antranílicas bicíclicas de fórmula (i) e intermediarios de las mismas |
Country Status (4)
| Country | Link |
|---|---|
| AR (1) | AR126248A1 (zh) |
| TW (1) | TW202317562A (zh) |
| UY (1) | UY39833A (zh) |
| WO (1) | WO2023275705A1 (zh) |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3728256A1 (en) | 2017-12-20 | 2020-10-28 | PI Industries Ltd. | Pyrazolopyridine-diamides, their use as insecticide and processes for preparing the same |
| EP3927685A4 (en) * | 2019-02-22 | 2022-11-23 | PI Industries Ltd. | PROCESS FOR THE SYNTHESIS OF ANTHRANILIC DIAMIDE COMPOUNDS AND ASSOCIATED INTERMEDIATES |
| WO2021010492A1 (en) * | 2019-07-17 | 2021-01-21 | Ono Pharmaceutical Co., Ltd. | Compound having kdm5 inhibitory activity and pharmaceutical use thereof |
| TW202220557A (zh) * | 2020-07-27 | 2022-06-01 | 印度商皮埃企業有限公司 | 包含吡唑並吡啶鄰氨基苯甲酰胺化合物、其氧化物或鹽的農藥活性混合物 |
-
2022
- 2022-06-27 WO PCT/IB2022/055939 patent/WO2023275705A1/en unknown
- 2022-06-27 AR ARP220101674A patent/AR126248A1/es unknown
- 2022-06-28 TW TW111124150A patent/TW202317562A/zh unknown
- 2022-06-28 UY UY0001039833A patent/UY39833A/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| WO2023275705A1 (en) | 2023-01-05 |
| UY39833A (es) | 2023-01-31 |
| TW202317562A (zh) | 2023-05-01 |
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