AR099989A1 - Proceso de preparación de (s)-1-(1-(4-cloro-3-fluorofenil)-2-hidroxietil)-4-(2-((1-metil-1h-pirazol-5-il)amino)pirimidin-4-il)-2(1h)-ona y sus sales - Google Patents
Proceso de preparación de (s)-1-(1-(4-cloro-3-fluorofenil)-2-hidroxietil)-4-(2-((1-metil-1h-pirazol-5-il)amino)pirimidin-4-il)-2(1h)-ona y sus salesInfo
- Publication number
- AR099989A1 AR099989A1 ARP150101063A ARP150101063A AR099989A1 AR 099989 A1 AR099989 A1 AR 099989A1 AR P150101063 A ARP150101063 A AR P150101063A AR P150101063 A ARP150101063 A AR P150101063A AR 099989 A1 AR099989 A1 AR 099989A1
- Authority
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- Argentina
- Prior art keywords
- formula
- compound
- approximately
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Links
- -1 1- (4-CHLORO-3-FLUOROPHENYL) -2-HYDROXYETHYL Chemical class 0.000 title abstract 3
- 238000002360 preparation method Methods 0.000 title abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 14
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 2
- 239000003795 chemical substances by application Substances 0.000 abstract 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- 239000003960 organic solvent Substances 0.000 abstract 2
- 238000000634 powder X-ray diffraction Methods 0.000 abstract 2
- ZNGGAPYUQROFJC-QMMMGPOBSA-N (1r)-1-(4-chloro-3-fluorophenyl)ethane-1,2-diol Chemical compound OC[C@H](O)C1=CC=C(Cl)C(F)=C1 ZNGGAPYUQROFJC-QMMMGPOBSA-N 0.000 abstract 1
- NAWXUBYGYWOOIX-SFHVURJKSA-N (2s)-2-[[4-[2-(2,4-diaminoquinazolin-6-yl)ethyl]benzoyl]amino]-4-methylidenepentanedioic acid Chemical compound C1=CC2=NC(N)=NC(N)=C2C=C1CCC1=CC=C(C(=O)N[C@@H](CC(=C)C(O)=O)C(O)=O)C=C1 NAWXUBYGYWOOIX-SFHVURJKSA-N 0.000 abstract 1
- FRSBDALHVZFPHT-UHFFFAOYSA-N 2-chloro-1-(4-chloro-3-fluorophenyl)ethanone Chemical compound FC1=CC(C(=O)CCl)=CC=C1Cl FRSBDALHVZFPHT-UHFFFAOYSA-N 0.000 abstract 1
- SCOJKGRNQDKFRP-UHFFFAOYSA-N 2-chloro-n-methoxy-n-methylacetamide Chemical compound CON(C)C(=O)CCl SCOJKGRNQDKFRP-UHFFFAOYSA-N 0.000 abstract 1
- JESRNIJXVIFVOV-UHFFFAOYSA-N 2-methylpyrazol-3-amine Chemical compound CN1N=CC=C1N JESRNIJXVIFVOV-UHFFFAOYSA-N 0.000 abstract 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 abstract 1
- AGYWDGVTLKNTBS-UHFFFAOYSA-N 4-bromo-1-chloro-2-fluorobenzene Chemical compound FC1=CC(Br)=CC=C1Cl AGYWDGVTLKNTBS-UHFFFAOYSA-N 0.000 abstract 1
- RAEXTEKKMYSCEX-UHFFFAOYSA-N CS(=O)(=O)C1=NC=CC(=N1)C1=CC(NC=C1)=O Chemical compound CS(=O)(=O)C1=NC=CC(=N1)C1=CC(NC=C1)=O RAEXTEKKMYSCEX-UHFFFAOYSA-N 0.000 abstract 1
- 101001110310 Lentilactobacillus kefiri NADP-dependent (R)-specific alcohol dehydrogenase Proteins 0.000 abstract 1
- 239000004280 Sodium formate Substances 0.000 abstract 1
- 239000000010 aprotic solvent Substances 0.000 abstract 1
- SRSXLGNVWSONIS-UHFFFAOYSA-M benzenesulfonate Chemical class [O-]S(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-M 0.000 abstract 1
- KOPOQZFJUQMUML-UHFFFAOYSA-N chlorosilane Chemical compound Cl[SiH3] KOPOQZFJUQMUML-UHFFFAOYSA-N 0.000 abstract 1
- 235000019253 formic acid Nutrition 0.000 abstract 1
- 238000006263 metalation reaction Methods 0.000 abstract 1
- 150000002901 organomagnesium compounds Chemical class 0.000 abstract 1
- 239000007800 oxidant agent Substances 0.000 abstract 1
- 239000003880 polar aprotic solvent Substances 0.000 abstract 1
- HLBBKKJFGFRGMU-UHFFFAOYSA-M sodium formate Chemical compound [Na+].[O-]C=O HLBBKKJFGFRGMU-UHFFFAOYSA-M 0.000 abstract 1
- 235000019254 sodium formate Nutrition 0.000 abstract 1
- YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical compound ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P17/00—Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms
- C12P17/16—Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms containing two or more hetero rings
- C12P17/165—Heterorings having nitrogen atoms as the only ring heteroatoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/13—Crystalline forms, e.g. polymorphs
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biotechnology (AREA)
- Genetics & Genomics (AREA)
- General Engineering & Computer Science (AREA)
- Microbiology (AREA)
- Biochemistry (AREA)
- Epidemiology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pyridine Compounds (AREA)
Abstract
Reivindicación 1: Un proceso para la preparación de un compuesto de fórmula (8), comprendiendo el proceso los pasos de: (a) contactar 4-bromo-1-cloro-2-fluorobenceno de fórmula (12) con un agente de metalación en un solvente orgánico aprótico para proporcionar un compuesto de organomagnesio, el cual se hace reaccionar con 2-cloro-N-metoxi-N-metilacetamida de fórmula (13) para proporcionar 2-cloro-1-(4-cloro-3-fluorofenil)etanona de fórmula (2); (b) contactar el compuesto de fórmula (2) con formiato sódico y ácido fórmico en etanol acuoso para proporcionar 1-(4-cloro-3-fluorofenil)-2-hidroxietanona de fórmula (3); (c) contactar el compuesto de fórmula (3) con una ceto reductasa para proporcionar (R)-1-(4-cloro-3-fluorofenil)etan-1,2-diol de fórmula (4); (d) contactar el compuesto de fórmula (4) con un cloruro de sililo (Rᵃ)₃SiCl y por lo menos una base en un solvente aprótico no polar para proporcionar el compuesto de fórmula (5), y posteriormente agregar cloruro de sulfonilo RᵇS(O)₂Cl para proporcionar el compuesto de fórmula (6); (e) contactar 4-(2-(metilsulfonil)pirimidin-4-il)piridin-2(1H)-ona de fórmula (7) con una base fuerte en un solvente orgánico y posteriormente agregar el compuesto de fórmula (6) para proporcionar el compuesto de fórmula (11); (f) tratar el compuesto de fórmula (11) con un agente oxidante para proporcionar el compuesto de fórmula (1); (g) tratar 1-metil-1H-pirazol-5-amina con una base fuerte en un solvente aprótico a temperatura reducida de fórmula (10) y agregar el compuesto de fórmula (1) para proporcionar el compuesto de fórmula (9); y, (h) contactar el compuesto de fórmula (9) con un agente des-sililante para proporcionar el compuesto de fórmula (8). Reivindicación 15: Una sal besilato cristalina de acuerdo con la reivindicación 14 donde el patrón de difracción de polvo de rayos X comprende por lo menos cinco picos de difracción de XRPD (expresados en grados 2q) seleccionados del grupo que consiste en aproximadamente 6.126, aproximadamente 14.679, aproximadamente 16.327, aproximadamente 17.358, aproximadamente 17.358, aproximadamente 19.716, aproximadamente 25.754, aproximadamente 25.942 y aproximadamente 26.976.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN2014075011 | 2014-04-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR099989A1 true AR099989A1 (es) | 2016-08-31 |
Family
ID=54287327
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP150101063A AR099989A1 (es) | 2014-04-09 | 2015-04-08 | Proceso de preparación de (s)-1-(1-(4-cloro-3-fluorofenil)-2-hidroxietil)-4-(2-((1-metil-1h-pirazol-5-il)amino)pirimidin-4-il)-2(1h)-ona y sus sales |
Country Status (22)
Country | Link |
---|---|
US (4) | US20170022183A1 (es) |
EP (2) | EP3129025B1 (es) |
JP (3) | JP6723926B2 (es) |
KR (3) | KR20230006043A (es) |
CN (3) | CN112645927A (es) |
AR (1) | AR099989A1 (es) |
AU (2) | AU2015245743B2 (es) |
BR (2) | BR122020014933B8 (es) |
CA (2) | CA2945098C (es) |
ES (1) | ES2733495T3 (es) |
HR (1) | HRP20191306T1 (es) |
IL (2) | IL248205B (es) |
MX (2) | MX2016013162A (es) |
MY (2) | MY196320A (es) |
NZ (1) | NZ725450A (es) |
PL (1) | PL3129025T3 (es) |
RU (1) | RU2684102C2 (es) |
SG (1) | SG11201608421XA (es) |
SI (1) | SI3129025T1 (es) |
TW (2) | TWI762806B (es) |
WO (1) | WO2015154674A1 (es) |
ZA (1) | ZA201607066B (es) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ES2857649T3 (es) * | 2012-03-01 | 2021-09-29 | Array Biopharma Inc | Inhibidores de serina/treonina cinasa |
US9532987B2 (en) | 2013-09-05 | 2017-01-03 | Genentech, Inc. | Use of a combination of a MEK inhibitor and an ERK inhibitor for treatment of hyperproliferative diseases |
CN106029672B (zh) | 2013-12-06 | 2019-03-29 | 基因泰克公司 | 丝氨酸/苏氨酸激酶抑制剂 |
ES2733495T3 (es) | 2014-04-09 | 2019-11-29 | Genentech Inc | Proceso para la fabricación de medicamentos |
TN2018000119A1 (en) | 2015-11-09 | 2019-10-04 | Astrazeneca Ab | Dihydroimidazopyrazinone derivatives useful in the treatment of cancer |
AU2017249229A1 (en) | 2016-04-15 | 2018-10-04 | Genentech, Inc. | Diagnostic and therapeutic methods for cancer |
TWI827550B (zh) | 2017-09-08 | 2024-01-01 | 美商建南德克公司 | 癌症之診斷及治療方法 |
US20210008047A1 (en) | 2018-02-13 | 2021-01-14 | Vib Vzw | Targeting minimal residual disease in cancer with rxr antagonists |
CN114746410A (zh) * | 2019-12-05 | 2022-07-12 | 阿斯利康有限公司 | 用于生产式(i)的方法和中间体 |
CN115710158A (zh) * | 2021-08-23 | 2023-02-24 | 凯特立斯(深圳)科技有限公司 | 一种不对称催化制备替格瑞洛中间体的方法 |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
MY130778A (en) * | 2001-02-09 | 2007-07-31 | Vertex Pharma | Heterocyclic inhibitiors of erk2 and uses thereof |
US6869966B2 (en) * | 2002-09-30 | 2005-03-22 | Banyu Pharmaceutical Co., Ltd. | N-substituted-2-oxodihydropyridine derivatives |
AU2007229552C1 (en) * | 2006-03-29 | 2013-06-13 | F. Hoffmann-La Roche Ag | Pyridine and pyrimidine derivatives as mGluR2 antagonists |
WO2009061761A2 (en) * | 2007-11-06 | 2009-05-14 | E. I. Du Pont De Nemours And Company | Fungicidal heterocyclic amines |
ES2857649T3 (es) * | 2012-03-01 | 2021-09-29 | Array Biopharma Inc | Inhibidores de serina/treonina cinasa |
WO2015130976A1 (en) * | 2014-02-27 | 2015-09-03 | Canon U.S.A., Inc. | Placement apparatus |
ES2733495T3 (es) | 2014-04-09 | 2019-11-29 | Genentech Inc | Proceso para la fabricación de medicamentos |
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2015
- 2015-04-08 ES ES15776904T patent/ES2733495T3/es active Active
- 2015-04-08 AU AU2015245743A patent/AU2015245743B2/en active Active
- 2015-04-08 EP EP15776904.3A patent/EP3129025B1/en active Active
- 2015-04-08 TW TW108130327A patent/TWI762806B/zh active
- 2015-04-08 CN CN202011466648.XA patent/CN112645927A/zh active Pending
- 2015-04-08 MX MX2016013162A patent/MX2016013162A/es active IP Right Grant
- 2015-04-08 WO PCT/CN2015/076083 patent/WO2015154674A1/en active Application Filing
- 2015-04-08 PL PL15776904T patent/PL3129025T3/pl unknown
- 2015-04-08 CN CN201580029835.2A patent/CN106659721B/zh active Active
- 2015-04-08 BR BR122020014933A patent/BR122020014933B8/pt active IP Right Grant
- 2015-04-08 SG SG11201608421XA patent/SG11201608421XA/en unknown
- 2015-04-08 MY MYPI2021005412A patent/MY196320A/en unknown
- 2015-04-08 EP EP19152874.4A patent/EP3494971A1/en active Pending
- 2015-04-08 BR BR112016023391-3A patent/BR112016023391B1/pt active IP Right Grant
- 2015-04-08 KR KR1020227045548A patent/KR20230006043A/ko active IP Right Grant
- 2015-04-08 NZ NZ725450A patent/NZ725450A/en unknown
- 2015-04-08 RU RU2016139286A patent/RU2684102C2/ru active
- 2015-04-08 SI SI201530799T patent/SI3129025T1/sl unknown
- 2015-04-08 CN CN202010547624.0A patent/CN111777594B/zh active Active
- 2015-04-08 MY MYPI2016001816A patent/MY188526A/en unknown
- 2015-04-08 AR ARP150101063A patent/AR099989A1/es unknown
- 2015-04-08 KR KR1020167030901A patent/KR102490955B1/ko active IP Right Grant
- 2015-04-08 CA CA2945098A patent/CA2945098C/en active Active
- 2015-04-08 MX MX2020010384A patent/MX2020010384A/es unknown
- 2015-04-08 CA CA3167641A patent/CA3167641A1/en active Pending
- 2015-04-08 KR KR1020207009606A patent/KR20200038553A/ko not_active Application Discontinuation
- 2015-04-08 TW TW104111317A patent/TWI678366B/zh active
- 2015-04-08 JP JP2016561841A patent/JP6723926B2/ja active Active
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2016
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- 2016-10-06 IL IL248205A patent/IL248205B/en active IP Right Grant
- 2016-10-13 ZA ZA2016/07066A patent/ZA201607066B/en unknown
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2018
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2019
- 2019-07-18 HR HRP20191306TT patent/HRP20191306T1/hr unknown
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- 2019-08-13 IL IL26869019A patent/IL268690A/en unknown
- 2019-12-18 US US16/718,602 patent/US11066389B2/en active Active
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- 2020-03-02 JP JP2020035010A patent/JP6974524B2/ja active Active
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2021
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