AR112278A1 - Proceso mejorado para la preparación de productos intermedios - Google Patents
Proceso mejorado para la preparación de productos intermediosInfo
- Publication number
- AR112278A1 AR112278A1 ARP180102002A AR112278A1 AR 112278 A1 AR112278 A1 AR 112278A1 AR P180102002 A ARP180102002 A AR P180102002A AR 112278 A1 AR112278 A1 AR 112278A1
- Authority
- AR
- Argentina
- Prior art keywords
- chlorocyclopropyl
- chlorophenyl
- chloro
- reacting
- prothioconazole
- Prior art date
Links
- 238000000034 method Methods 0.000 title abstract 2
- 239000013067 intermediate product Substances 0.000 title 1
- MNHVNIJQQRJYDH-UHFFFAOYSA-N 2-[2-(1-chlorocyclopropyl)-3-(2-chlorophenyl)-2-hydroxypropyl]-1,2-dihydro-1,2,4-triazole-3-thione Chemical compound N1=CNC(=S)N1CC(C1(Cl)CC1)(O)CC1=CC=CC=C1Cl MNHVNIJQQRJYDH-UHFFFAOYSA-N 0.000 abstract 4
- 239000005825 Prothioconazole Substances 0.000 abstract 4
- -1 2-chlorobenzyl halide Chemical class 0.000 abstract 3
- JWUJQDFVADABEY-UHFFFAOYSA-N 2-methyltetrahydrofuran Chemical compound CC1CCCO1 JWUJQDFVADABEY-UHFFFAOYSA-N 0.000 abstract 3
- 238000004519 manufacturing process Methods 0.000 abstract 3
- 239000002904 solvent Substances 0.000 abstract 3
- LGNKJFHEXZRYDM-UHFFFAOYSA-N 1-chloro-2-(1-chlorocyclopropyl)-3-(2-chlorophenyl)propan-2-ol Chemical compound C1CC1(Cl)C(CCl)(O)CC1=CC=CC=C1Cl LGNKJFHEXZRYDM-UHFFFAOYSA-N 0.000 abstract 2
- IKKKLHQSHUAIMM-UHFFFAOYSA-N 2-(1-chlorocyclopropyl)-2-[(2-chlorophenyl)methyl]oxirane Chemical compound ClC1=CC=CC=C1CC1(C2(Cl)CC2)OC1 IKKKLHQSHUAIMM-UHFFFAOYSA-N 0.000 abstract 2
- NSPMIYGKQJPBQR-UHFFFAOYSA-N 4H-1,2,4-triazole Chemical compound C=1N=CNN=1 NSPMIYGKQJPBQR-UHFFFAOYSA-N 0.000 abstract 1
- HHUQPWODPBDTLI-UHFFFAOYSA-N Prothioconazole-desthio Chemical compound C1=NC=NN1CC(C1(Cl)CC1)(O)CC1=CC=CC=C1Cl HHUQPWODPBDTLI-UHFFFAOYSA-N 0.000 abstract 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
- 239000011593 sulfur Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D301/00—Preparation of oxiranes
- C07D301/27—Condensation of epihalohydrins or halohydrins with compounds containing active hydrogen atoms
- C07D301/28—Condensation of epihalohydrins or halohydrins with compounds containing active hydrogen atoms by reaction with hydroxyl radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
- C07D249/10—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D249/12—Oxygen or sulfur atoms
-
- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/12—Powders or granules
-
- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/132—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group
- C07C29/136—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH
- C07C29/143—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of ketones
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/36—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring increasing the number of carbon atoms by reactions with formation of hydroxy groups, which may occur via intermediates being derivatives of hydroxy, e.g. O-metal
- C07C29/38—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring increasing the number of carbon atoms by reactions with formation of hydroxy groups, which may occur via intermediates being derivatives of hydroxy, e.g. O-metal by reaction with aldehydes or ketones
- C07C29/40—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring increasing the number of carbon atoms by reactions with formation of hydroxy groups, which may occur via intermediates being derivatives of hydroxy, e.g. O-metal by reaction with aldehydes or ketones with compounds containing carbon-to-metal bonds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D301/00—Preparation of oxiranes
- C07D301/02—Synthesis of the oxirane ring
- C07D301/24—Synthesis of the oxirane ring by splitting off HAL—Y from compounds containing the radical HAL—C—C—OY
- C07D301/26—Y being hydrogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/06—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/02—Systems containing only non-condensed rings with a three-membered ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Environmental Sciences (AREA)
- Dentistry (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Toxicology (AREA)
- Epoxy Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
En la presente solicitud se describe un proceso para preparar 1-cloro-2-(1-clorociclopropil)-3-(2-clorofenil)propan-2-ol y 2-(1-clorociclopropil)-2-[(2-clorofenil)metil]oxirano. Reivindicación 1: Un proceso para la preparación de 1-cloro-2-(1-clorociclopropil)-3-(2-clorofenil)propan-2-ol y 2-(1-clorociclopropil)-2-[(2-clorofenil)metil]oxirano o una mezcla de estos al hacer reaccionar haluro de 2-clorobencilo con 1-cloro-1-cloroacetilciclopropano caracterizado porque la reacción se lleva a cabo en un sistema solvente que comprende metil tetrahidrofurano. Reivindicación 6: Un proceso para preparar protioconazol caracterizado porque comprende: (a) hacer reaccionar haluro de 2-clorobencilo con 1-cloro-1-cloroacetilciclopropano en un sistema solvente que comprende metil tetrahidrofurano; y (b) usar el producto de la etapa (a) para preparar protioconazol. Reivindicación 7: Un proceso para preparar protioconazol caracterizado porque comprende: (a) hacer reaccionar haluro de 2-clorobencilo con 1-cloro-1-cloroacetilciclopropano en un sistema solvente que comprende tetrahidrofurano de metilo; (a) hacer reaccionar el producto de la etapa (a) con 1,2,4-triazol para producir 2-(1-clorociclopropil)-1-(2-clorofenil)-3-(1H-1,2,4-triazol-1-il)propan-2-ol; y (c) hacer reaccionar el producto de la etapa (b) con azufre para producir protioconazol.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IN201831008255 | 2018-03-06 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR112278A1 true AR112278A1 (es) | 2019-10-09 |
Family
ID=67512127
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP180102002 AR112278A1 (es) | 2018-03-06 | 2018-07-18 | Proceso mejorado para la preparación de productos intermedios |
Country Status (9)
Country | Link |
---|---|
US (1) | US20200399236A1 (es) |
EP (2) | EP3762356A4 (es) |
CN (1) | CN112399967A (es) |
AR (1) | AR112278A1 (es) |
CA (1) | CA3093047A1 (es) |
EA (1) | EA202091920A1 (es) |
UA (1) | UA127895C2 (es) |
UY (1) | UY37792A (es) |
WO (1) | WO2019171161A1 (es) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IN201921042108A (es) * | 2019-10-17 | 2021-04-23 | ||
CN114085126B (zh) * | 2021-10-09 | 2023-09-29 | 张北北九食品检验技术有限公司 | 放射性同位素碳-14标记的苄基化合物、丙硫菌唑及其制备方法和在代谢实验中的应用 |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3812967A1 (de) * | 1987-06-24 | 1989-01-05 | Bayer Ag | Azolylmethyl-cyclopropyl-derivate |
DE3942240A1 (de) * | 1989-12-21 | 1991-06-27 | Bayer Ag | Azolylmethyl-cyclopropyl-saccharinaddukte |
DE4027608A1 (de) * | 1990-08-31 | 1992-03-05 | Bayer Ag | Verfahren zur herstellung von 1-chlor-2-(1-chlor-cyclopropyl)-3-(2-chlor-phenyl)-propan-2-ol und/oder 2-(1-chlor-cyclopropyl)-2-(2-chlor-benzyl)-oxiran |
DE4030039A1 (de) * | 1990-09-22 | 1992-03-26 | Bayer Ag | Verfahren zur herstellung von 2-(1-chlor-cyclopropyl)-1- (2-chlor-phenyl)-3-(1,2,4-triazol-1-yl- propan-2-ol |
DE19808570C1 (de) | 1998-02-28 | 1999-03-04 | Metallgesellschaft Ag | Benzylmagnesiumhalogenide oder Allylmagnesiumhalogenide enthaltende Synthesemittel und Verfahren zu deren Herstellung |
DE10233171A1 (de) * | 2002-07-22 | 2004-02-12 | Bayer Cropscience Ag | Kristallmodifikation II des 2-[2-(Chlor-cyclopropyl)-3-(2-chlorphenyl)-2-hydroxy-propyl]-2,4dihydro-3H-1,2,4-triazol-3-thions |
CN105263911A (zh) * | 2012-12-21 | 2016-01-20 | 巴斯夫欧洲公司 | 取代[1,2,4]三唑和咪唑化合物 |
CN104557742A (zh) | 2013-10-15 | 2015-04-29 | 上海生华化学科技有限公司 | 一种丙硫菌唑类似物的制备方法 |
CN106749057B (zh) * | 2016-12-30 | 2019-07-30 | 南京工业大学 | 一种中间体化合物以及丙硫菌唑的合成方法 |
CN106928041A (zh) | 2017-03-02 | 2017-07-07 | 芮城县斯普伦迪生物工程有限公司 | 一种2‑氯苄基‑(1‑氯环丙基)酮的制备方法 |
CN107628928A (zh) * | 2017-09-27 | 2018-01-26 | 长治市晋宁化工有限公司 | 2‑(1‑氯‑环丙烷‑1‑基)‑3‑氯‑1‑(2‑氯‑苯基)‑2‑丙醇的制备方法 |
-
2018
- 2018-06-04 EP EP18908969.1A patent/EP3762356A4/en not_active Withdrawn
- 2018-06-04 CN CN201880090871.3A patent/CN112399967A/zh active Pending
- 2018-06-04 WO PCT/IB2018/053974 patent/WO2019171161A1/en unknown
- 2018-06-04 EA EA202091920A patent/EA202091920A1/ru unknown
- 2018-06-04 CA CA3093047A patent/CA3093047A1/en active Pending
- 2018-06-04 US US16/977,638 patent/US20200399236A1/en active Pending
- 2018-06-04 UA UAA202005814A patent/UA127895C2/uk unknown
- 2018-06-04 EP EP24173628.9A patent/EP4385329A2/en active Pending
- 2018-07-02 UY UY0001037792A patent/UY37792A/es unknown
- 2018-07-18 AR ARP180102002 patent/AR112278A1/es unknown
Also Published As
Publication number | Publication date |
---|---|
CA3093047A1 (en) | 2019-09-12 |
EP3762356A1 (en) | 2021-01-13 |
EP3762356A4 (en) | 2021-09-29 |
EP4385329A2 (en) | 2024-06-19 |
US20200399236A1 (en) | 2020-12-24 |
UA127895C2 (uk) | 2024-02-07 |
BR102018015115A2 (pt) | 2019-09-17 |
AU2018411552A1 (en) | 2020-10-08 |
UY37792A (es) | 2019-04-30 |
EA202091920A1 (ru) | 2020-10-27 |
WO2019171161A8 (en) | 2020-11-05 |
CN112399967A (zh) | 2021-02-23 |
WO2019171161A1 (en) | 2019-09-12 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
MX2018007513A (es) | Metodo para producir 2-[4-(4-clorofenoxi)-2-(trifluorometil)fenil] -1-(1,2,4-triazol-1-il)propan-2-ol. | |
AR112278A1 (es) | Proceso mejorado para la preparación de productos intermedios | |
CL2014000125A1 (es) | Compuesto fungicidas de 1-(2-(2-halo-4-(4-halogen-fenoxi)-fenil)-2-etoxi-etil)-1h-(1,2,4)triazol sustituidos; procesos para preparar dichos compuestos; uso de dichos compuestos para combatir hongos fitopatógenos. | |
PE20080990A1 (es) | Azolilmetiloxiranos, su uso para combatir hongos fitopatogenos, asi como productos que los contienen | |
AR106728A1 (es) | 4-((6-(2-(2,4difluorofenil)-1,1-difluoro-2-hidroxi-3-(1h-1,2,4-triazol-1-il)propil)piridin-3-il)oxi)benzonitrilo y proceso para su preparación | |
SG11202102057SA (en) | Process for the preparation of methyl 6-(2,4-dichlorophenyl)-5-[4-[(3s)-1-(3-fluoropropyl)pyrrolidin-3-yl]oxyphenyl]-8,9-dihydro-7h-benzo[7]annulene-2-carboxylate | |
AR106731A1 (es) | 4-((6-(2-(2,4-difluorofenil)-1,1-difluoro-2-hidroxi-3-(1h-1,2,4-triazol-1-il)propil)piridin-3-il)oxi)benzonitrilo y proceso para su preparación | |
AR106730A1 (es) | 4-((6-(2-(2,4-difluorofenil)-1,1-difluoro-2-hidroxi-3-(1h-1,2,4-triazol-1-il)propil)piridin-3-il)oxi)benzonitrilo y proceso para su preparación | |
WO2007013096A8 (en) | Improved process for the preparation of 2r, 3s-2-(2,4-difluorophenyl)-3-(5-fluoropyrimidin-4-yl)-1-(1h-1,2,4-triazol-1-yl) butan-2-ol (voriconazole) | |
EP3060559A4 (en) | Improved process for the preparation of ((3s,5r)-5-((1h-1,2,4-triazol-1-yl)methyl)-5-(2,4-difluorophenyl)tetrahydrofuran-3-yl)methyl-4-methylbenzenesulfonate | |
NZ206251A (en) | Hydroxyalkyl-azolyl derivatives and fungicidal compositions | |
MX2022005229A (es) | Un nuevo proceso eficaz para la sintesis de 2-amino-5-cloro-n,3-di metilbenzamida. | |
MX2019014836A (es) | Formulaciones estabilizadas que contienen protioconazol con bajo contenido de 2-(1-clorociclopropanil)-1-(2-clorofenil)-3-(1h-1,2,4 -triazol-1-il)propan-2-ol. | |
EP3827099A4 (en) | SMALL RNA PREDICTORS FOR ALZHEIMER'S DISEASE | |
ECSP20023056A (es) | Profármacos de derivados de triazol sustituido y sus usos | |
EP3835427A4 (en) | PROCESS FOR GENERATION OF 3,5-DIHYDROXY-4-METHOXYBENZYL ALCOHOL FROM PLANKTON | |
GB2450268A (en) | Synthesis of 4-[1-(4-Cyano Phenyl)-(1,2,4-Triazol-1-YL)Methyl] Benzonitrile and 4-[1-(1-H-1,2,4-Triazol-1-YL)Methylene Benzonitrile Intermediate | |
BR102013027313A8 (pt) | processo para a preparação seletiva de (1h-1,2,4-triazol-1-il) alcanóis, composto hidrazinil alcanol obtido por tal processo e seu uso | |
WO2008075163A3 (en) | An improved process for the preparation of rizatriptan | |
EP4095121A4 (en) | PROCESS FOR OBTAINING COMPOUNDS, INCLUDING TRIPTANE, BY ALCOHOL COUPLING REACTION | |
EP0090993A3 (en) | Substituted hydroxyalkyl azoles, process for preparing them and their use as antimycotics | |
RU2256655C1 (ru) | Способ получения 1-(4-хлорфенил)-3-(1,2,4-триазол-1-ил-метил)-4,4-диметилпентан-3-ола | |
ES2064351T3 (es) | Procedimiento para la isomerizacion de triazoles simetricos a triazoles asimetricos. | |
MD4505C1 (ro) | Procedeu de sinteză a 3,3-dimetil-1-(1H-1,2,4-triazol-1-il)butan-2-onei | |
PE20231013A1 (es) | Procesos e intermedios para la preparacion de (s)-5-amino-3-(4-((5-fluoro-2-metoxibenzamido)metil)fenil)-1-(1,1,1-trifluoropropan-2-il)-1h-pirazol-4-carboxamida |