PL430867A1 - Iminowe pochodne aldehydów salicylowych i hydrazydów kwasowych, sposób ich wytwarzania oraz ich zastosowanie - Google Patents
Iminowe pochodne aldehydów salicylowych i hydrazydów kwasowych, sposób ich wytwarzania oraz ich zastosowanieInfo
- Publication number
- PL430867A1 PL430867A1 PL430867A PL43086719A PL430867A1 PL 430867 A1 PL430867 A1 PL 430867A1 PL 430867 A PL430867 A PL 430867A PL 43086719 A PL43086719 A PL 43086719A PL 430867 A1 PL430867 A1 PL 430867A1
- Authority
- PL
- Poland
- Prior art keywords
- hoc6h4
- ch3oc6h4
- formula
- salicylaldehydes
- acid hydrazides
- Prior art date
Links
- 229940042795 hydrazides for tuberculosis treatment Drugs 0.000 title abstract 5
- 239000002253 acid Substances 0.000 title abstract 4
- 150000002466 imines Chemical class 0.000 title abstract 3
- 238000002360 preparation method Methods 0.000 title abstract 2
- 150000001299 aldehydes Chemical class 0.000 title 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 abstract 6
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 abstract 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract 3
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 3
- SMQUZDBALVYZAC-UHFFFAOYSA-N salicylaldehyde Chemical compound OC1=CC=CC=C1C=O SMQUZDBALVYZAC-UHFFFAOYSA-N 0.000 abstract 2
- 239000002904 solvent Substances 0.000 abstract 2
- OFLXLNCGODUUOT-UHFFFAOYSA-N acetohydrazide Chemical compound C\C(O)=N\N OFLXLNCGODUUOT-UHFFFAOYSA-N 0.000 abstract 1
- 230000002378 acidificating effect Effects 0.000 abstract 1
- 229940121375 antifungal agent Drugs 0.000 abstract 1
- 239000003429 antifungal agent Substances 0.000 abstract 1
- 238000009835 boiling Methods 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 239000011814 protection agent Substances 0.000 abstract 1
- 239000000376 reactant Substances 0.000 abstract 1
- 239000011541 reaction mixture Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C243/00—Compounds containing chains of nitrogen atoms singly-bound to each other, e.g. hydrazines, triazanes
- C07C243/24—Hydrazines having nitrogen atoms of hydrazine groups acylated by carboxylic acids
- C07C243/38—Hydrazines having nitrogen atoms of hydrazine groups acylated by carboxylic acids with acylating carboxyl groups bound to carbon atoms of six-membered aromatic rings
-
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
- A01N37/28—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof containing the group; Thio analogues thereof
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01P—BIOCIDAL, PEST REPELLANT, PEST ATTRACTANT OR PLANT GROWTH REGULATORY ACTIVITY OF CHEMICAL COMPOUNDS OR PREPARATIONS
- A01P3/00—Fungicides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C243/00—Compounds containing chains of nitrogen atoms singly-bound to each other, e.g. hydrazines, triazanes
- C07C243/24—Hydrazines having nitrogen atoms of hydrazine groups acylated by carboxylic acids
- C07C243/26—Hydrazines having nitrogen atoms of hydrazine groups acylated by carboxylic acids with acylating carboxyl groups bound to hydrogen atoms or to acyclic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C249/00—Preparation of compounds containing nitrogen atoms doubly-bound to a carbon skeleton
- C07C249/16—Preparation of compounds containing nitrogen atoms doubly-bound to a carbon skeleton of hydrazones
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C251/00—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton
- C07C251/72—Hydrazones
- C07C251/86—Hydrazones having doubly-bound carbon atoms of hydrazone groups bound to carbon atoms of six-membered aromatic rings
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Environmental Sciences (AREA)
- Wood Science & Technology (AREA)
- Plant Pathology (AREA)
- Zoology (AREA)
- Engineering & Computer Science (AREA)
- Pest Control & Pesticides (AREA)
- General Health & Medical Sciences (AREA)
- Dentistry (AREA)
- Health & Medical Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Microbiology (AREA)
- Mycology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pyridine Compounds (AREA)
Abstract
Przedmiotem wynalazku są iminowe pochodne aldehydów salicylowych i hydrazydów kwasowych o wzorze 6 lub o wzorze ogólnym 1, w którym R1 oznacza H, t-Bu, Ph, R2 oznacza H, CH3, t-Bu, R3 oznacza H, OCH3, R4 oznacza Ph, 2-HOC6H4, 3-HOC6H4, 4-HOC6H4, 3-CH3OC6H4, 4-CH3OC6H4, 3,5-(HO)2C6H3, 3-pirydyl, 2-(1-HO-naftyl) a n stanowi liczbę 0 lub 1. Wynalazek dotyczy również sposobu wytwarzania iminowych pochodnych aldehydów salicylowych i hydrazydów kwasowych przedstawionych wzorem 6 lub wzorem ogólnym 1, w którym R1 oznacza H, t-Bu, Ph, R2 oznacza H, CH3, t-Bu, R3 oznacza H, OCH3, R4 oznacza Ph, 2-HOC6H4, 3-HOC6H4, 4-HOC6H4, 3-CH3OC6H4, 4-CH3OC6H4, 3,5-(HO)2C6H3, 3-pirydyl, 2-(1-HO-nafty1) a n stanowi liczbę 0 lub 1, polegający na tym, że równomolową mieszaninę aldehydu salicylowego o wzorze 4 lub aldehydów salicylowych o wzorze ogólnym 2, w którym R1 oznacza H, t-Bu, Ph, R2 oznacza H, CH3, t-Bu, R3 oznacza H, OCH3, oraz hydrazydu kwasu octowego 5 lub hydrazydów kwasowych o wzorze ogólnym 3, w których R4 oznacza Ph, 2-HOC6H4, 3-HOC6H4, 4-HOC6H4, 3-CH3OC6H4, 4-CH3OC6H4, 3,5-(HO)2C6H3, 3-pirydyl, 2-(1-HO-naftyl) a n stanowi liczbę 0 lub 1 w rozpuszczalniku traktuje się kwasem octowym i reakcję prowadzi się we wrzącym rozpuszczalniku w temperaturze 338 K do praktycznego przereagowania substratów a następnie z mieszaniny poreakcyjnej wydziela się produkty. Przedmiot wynalazku ujawnia zastosowanie hydrazydo-hydrazonów pochodnych hydrazydów kwasowych i aldehydów salicylowych jako środków ochrony roślin, zwłaszcza środków przeciwgrzybicznych.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PL430867A PL241843B1 (pl) | 2019-08-13 | 2019-08-13 | Iminowe pochodne aldehydów salicylowych i hydrazydów kwasowych, sposób ich wytwarzania oraz ich zastosowanie |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PL430867A PL241843B1 (pl) | 2019-08-13 | 2019-08-13 | Iminowe pochodne aldehydów salicylowych i hydrazydów kwasowych, sposób ich wytwarzania oraz ich zastosowanie |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| PL430867A1 true PL430867A1 (pl) | 2021-02-22 |
| PL241843B1 PL241843B1 (pl) | 2022-12-12 |
Family
ID=74647741
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL430867A PL241843B1 (pl) | 2019-08-13 | 2019-08-13 | Iminowe pochodne aldehydów salicylowych i hydrazydów kwasowych, sposób ich wytwarzania oraz ich zastosowanie |
Country Status (1)
| Country | Link |
|---|---|
| PL (1) | PL241843B1 (pl) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN118164872A (zh) * | 2024-03-12 | 2024-06-11 | 贵州大学 | 一类含席夫碱核心骨架的丁香酚类化合物及其制备方法和应用 |
-
2019
- 2019-08-13 PL PL430867A patent/PL241843B1/pl unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN118164872A (zh) * | 2024-03-12 | 2024-06-11 | 贵州大学 | 一类含席夫碱核心骨架的丁香酚类化合物及其制备方法和应用 |
Also Published As
| Publication number | Publication date |
|---|---|
| PL241843B1 (pl) | 2022-12-12 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Sujatha et al. | Synthesis and antiviral activity of 4, 4′-(arylmethylene) bis (1H-pyrazol-5-ols) against peste des petits ruminant virus (PPRV) | |
| MY159364A (en) | Fungicidal pyrazoles | |
| Rostami et al. | Sulfamic acid as a reusable and green catalyst for efficient and simple synthesis of 2-substituted-2, 3-dihydroquinazolin-4 (1H)-ones in water or methanol | |
| ATE497957T1 (de) | Pyridinderivate als fungizide verbindungen | |
| AR067896A1 (es) | Procedimiento para sintetizar compuestos utiles para tratar hepatitis c | |
| Wróbel et al. | Simple synthesis of N-aryl-2-nitrosoanilines in the reaction of nitroarenes with aniline anion derivatives | |
| EP0418667A2 (de) | Carbonsäureamide | |
| Bairagi et al. | Design, Synthesis and Evaluation of Schiff’s Bases of 4‐Chloro‐3‐coumarin aldehyde as Antimicrobial Agents | |
| Herbert Hall et al. | Syntheses and photophysical properties of some 5 (2)‐aryl‐2 (5)‐(4‐pyridyl) oxazoles and related oxadiazoles and furans | |
| PL430867A1 (pl) | Iminowe pochodne aldehydów salicylowych i hydrazydów kwasowych, sposób ich wytwarzania oraz ich zastosowanie | |
| Christie et al. | Preparation of highly substituted pyrrolidines via an organometallic dipole | |
| Wu et al. | Progress of Trifluoroacetoacetate in the Synthesis of Agrochemicals and Medicines with Fluorine | |
| Ghashang | Bismuth nitrate as an efficient catalyst for the preparation of 2-arylbenzothiazole derivatives | |
| Breuer et al. | Consecutive Alkynylation–Michael Addition–Cyclocondensation (AMAC) Multicomponent Syntheses of α-Pyrones and α-Pyridones | |
| Yu et al. | Synthesis and fungicidal activity of (E)-5-[1-(4-phenyl-2-oxo-1-oxaspiro [4.5] dec-3-en-3-yl) ethylidene]-2-aminoimidazolin-4-one derivatives | |
| Yazdani-Elah-Abadi et al. | Microwave Domino Diastereoselective Synthesis of Novel trans-4, 5-Dihydro-1 H-Furo [2, 3-c] Pyrazoles Using Pyridinium Salts in an Aqueous Medium | |
| Obydennov et al. | Synthesis of 4-oxothiazolidine-2, 5-diylidenes containing thioamide group based on dithiomalonamides | |
| SU677657A3 (ru) | Способ получени -формилированных соединений | |
| Yadigarov et al. | Reaction of 3-Chloro-1-(2, 4, 6-trimethylphenyl) propan-2-one with Amines. | |
| Bondarenko et al. | Reaction of natural isoflavonoids and their analogs with hydroxylamine | |
| DE602006020196D1 (de) | Verfahren zur herstellung einer 3-o-alkylascorbinsäure | |
| Rajora et al. | Microwave assisted transformation of benzimidazolyl chalcones into N1-substituted pyrazolines and evaluation of their antimicrobial activities | |
| Zhang et al. | Iodine-catalyzed three-component reaction of quinazoline-2, 5-diones with aldehydes and styrenes for the synthesis of allylamine derivatives | |
| Dyachenko | Novel method of 4, 6-dimethyl-2-thioxo-1, 2-dihydronicotinonitrile synthesis | |
| De Sarlo et al. | Condensation of Primary Nitro Compounds to Isoxazole Derivatives: Stoichiometric to Catalytic |