PE20211395A1 - Proceso de preparacion de dos derivados de 4-{[(2s)-2-{4-[5-cloro-2-(1h-1,2,3-triazol-1-il)fenil]-5-metoxi-2-oxopiridin-1(2h)-il}butanoil]amino}-2-fluorobenzamida - Google Patents
Proceso de preparacion de dos derivados de 4-{[(2s)-2-{4-[5-cloro-2-(1h-1,2,3-triazol-1-il)fenil]-5-metoxi-2-oxopiridin-1(2h)-il}butanoil]amino}-2-fluorobenzamidaInfo
- Publication number
- PE20211395A1 PE20211395A1 PE2020001408A PE2020001408A PE20211395A1 PE 20211395 A1 PE20211395 A1 PE 20211395A1 PE 2020001408 A PE2020001408 A PE 2020001408A PE 2020001408 A PE2020001408 A PE 2020001408A PE 20211395 A1 PE20211395 A1 PE 20211395A1
- Authority
- PE
- Peru
- Prior art keywords
- chloro
- triazol
- phenyl
- fluorobenzamide
- amino
- Prior art date
Links
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 title 1
- VCCBXIRSNXUBQG-UHFFFAOYSA-N 4-[5-chloro-2-(4-chlorotriazol-1-yl)phenyl]-5-methoxy-1H-pyridin-2-one Chemical compound ClC=1C=CC(=C(C=1)C1=CC(NC=C1OC)=O)N1N=NC(=C1)Cl VCCBXIRSNXUBQG-UHFFFAOYSA-N 0.000 abstract 1
- ASMGZJJSJBTIQV-UHFFFAOYSA-N 4-[5-chloro-2-[4-(trifluoromethyl)triazol-1-yl]phenyl]-5-methoxy-1H-pyridin-2-one Chemical compound COC1=CNC(=O)C=C1C1=C(C=CC(Cl)=C1)N1C=C(N=N1)C(F)(F)F ASMGZJJSJBTIQV-UHFFFAOYSA-N 0.000 abstract 1
- QLYMODAZQKOBHU-MRVPVSSYSA-N 4-[[(2R)-2-bromobutanoyl]amino]-2-fluorobenzamide Chemical compound Br[C@@H](C(=O)NC1=CC(=C(C(=O)N)C=C1)F)CC QLYMODAZQKOBHU-MRVPVSSYSA-N 0.000 abstract 1
- FPAKZDLGEHHCTC-IBGZPJMESA-N 4-[[(2S)-2-[4-[5-chloro-2-(4-chlorotriazol-1-yl)phenyl]-5-methoxy-2-oxopyridin-1-yl]butanoyl]amino]-2-fluorobenzamide Chemical compound CC[C@H](N1C=C(OC)C(=CC1=O)C1=C(C=CC(Cl)=C1)N1C=C(Cl)N=N1)C(=O)NC1=CC(F)=C(C=C1)C(N)=O FPAKZDLGEHHCTC-IBGZPJMESA-N 0.000 abstract 1
- XYWIPYBIIRTJMM-IBGZPJMESA-N 4-[[(2S)-2-[4-[5-chloro-2-[4-(trifluoromethyl)triazol-1-yl]phenyl]-5-methoxy-2-oxopyridin-1-yl]butanoyl]amino]-2-fluorobenzamide Chemical compound CC[C@H](N1C=C(OC)C(=CC1=O)C1=C(C=CC(Cl)=C1)N1C=C(N=N1)C(F)(F)F)C(=O)NC1=CC(F)=C(C=C1)C(N)=O XYWIPYBIIRTJMM-IBGZPJMESA-N 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 239000002904 solvent Substances 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
- C07D401/02—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
- C07D401/10—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 linked by a carbon chain containing aromatic 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
- C07C237/28—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a non-condensed six-membered aromatic ring of the carbon skeleton
- C07C237/30—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a non-condensed six-membered aromatic ring of the carbon skeleton having the nitrogen atom of the carboxamide group bound to hydrogen atoms or to acyclic carbon atoms
Abstract
La presente invencion se refiere a un proceso para preparar 4-{[(2S)-2-{4-[5-cloro-2-(4-cloro-1H-1,2,3-triazol-1-il)fenil]-5-metoxi-2-oxopiridin-1(2H)-il}butanoil]amino}-2-fluorobenzamida (formula I) o 4-({(2S)-2-[4-{5-cloro-2-[4-(trifluorometil)-1H-1,2,3-triazol-1-il]fenil}-5-metoxi-2-oxopiridin-1(2H)-il]butanoil}amino)-2-fluorobenzamida (formula II), caracterizado porque 4-[5-cloro-2-(4-cloro-1H-1,2,3-triazol-1-il)fenil]-5-metoxipiridin-2(1H)-ona (XVI-Cl) o 4-{5-cloro-2-[4-(trifluorometil)-1H-1,2,3-triazol-1-il]fenil}-5-metoxipiridin-2(1H)-ona (XVI-CF3) se hace reaccionar con 4-{[(2R)-2-bromobutanoil]amino}-2-fluorobenzamida (XIX) en presencia de una base en un solvente, posteriormente se aisla el compuesto de la formula (I) o (II).
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP18161983 | 2018-03-15 | ||
PCT/EP2019/055815 WO2019175043A1 (en) | 2018-03-15 | 2019-03-08 | Preparative process of two 4-{[(2s)-2-{4-[5-chloro-2-(1h-1,2,3-triazol-1-yl)phenyl]-5-methoxy-2-oxopyridin-1(2h)-yl}butanoyl]amino}-2-fluorobenzamide derivatives |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20211395A1 true PE20211395A1 (es) | 2021-07-27 |
Family
ID=61683650
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2020001408A PE20211395A1 (es) | 2018-03-15 | 2019-03-08 | Proceso de preparacion de dos derivados de 4-{[(2s)-2-{4-[5-cloro-2-(1h-1,2,3-triazol-1-il)fenil]-5-metoxi-2-oxopiridin-1(2h)-il}butanoil]amino}-2-fluorobenzamida |
Country Status (28)
Country | Link |
---|---|
US (1) | US11542245B2 (es) |
EP (2) | EP3889147A1 (es) |
JP (1) | JP7287978B2 (es) |
KR (1) | KR20200131241A (es) |
CN (1) | CN111770917B (es) |
AR (1) | AR117400A1 (es) |
AU (1) | AU2019236369B2 (es) |
BR (1) | BR112020018562A2 (es) |
CA (1) | CA3093733A1 (es) |
CL (1) | CL2020002371A1 (es) |
DK (1) | DK3765452T3 (es) |
ES (1) | ES2920449T3 (es) |
HR (1) | HRP20220565T1 (es) |
HU (1) | HUE058796T2 (es) |
IL (2) | IL300463A (es) |
JO (1) | JOP20200232B1 (es) |
LT (1) | LT3765452T (es) |
MX (1) | MX2020009580A (es) |
PE (1) | PE20211395A1 (es) |
PL (1) | PL3765452T3 (es) |
PT (1) | PT3765452T (es) |
RS (1) | RS63338B1 (es) |
SG (1) | SG11202006710RA (es) |
SI (1) | SI3765452T1 (es) |
TW (1) | TWI823911B (es) |
UA (1) | UA126940C2 (es) |
UY (1) | UY38147A (es) |
WO (1) | WO2019175043A1 (es) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20220140558A (ko) * | 2020-02-11 | 2022-10-18 | 케미노바 에이/에스 | (r)-2-아미노부탄산으로부터 s-베플루부타미드를 합성하는 방법 |
EP4304714A1 (en) | 2021-03-09 | 2024-01-17 | Bayer Aktiengesellschaft | Crystalline forms of (4s)-2 4-chloro-4-ethyl-7 3-fluoro-3 5-methoxy-3 2,5-dioxo-1 4-(trifluoromethyl)-3 2h-6-aza-3(4,1)-pyridina-1(1)-[1,2,3]triazola-2(1,2),7(1)-5 dibenzenaheptaphane-7 4-carboxamide |
WO2022189280A1 (en) | 2021-03-09 | 2022-09-15 | Bayer Aktiengesellschaft | Solvates of (4s)-24-chloro-4-ethyl-73-fluoro-35-methoxy-32,5-dioxo-14-(trifluoro-methyl)-32 h-6- aza-3(4,1)-pyridina-1(1)-[1,2,3]triazola-2(1,2),7(1)-dibenzenaheptaphane-74-carboxamide |
CA3212644A1 (en) | 2021-03-09 | 2022-09-15 | Bayer Aktiengesellschaft | Pharmaceutical dosage forms comprising (4s)-24-chloro-4-ethyl-73-fluoro-35-methoxy-32,5- dioxo-14-(trifluoromethyl)-32h-6-aza-3(4,1)-pyridina-1(1)-[1,2,3]triazola-2(1,2),7(1)- dibenzenaheptaphane-74-carboxamide |
WO2023174399A1 (zh) * | 2022-03-18 | 2023-09-21 | 苏州晶云药物科技股份有限公司 | 取代的氧代吡啶类衍生物的晶型及其制备方法 |
CN116535392B (zh) * | 2023-06-26 | 2023-09-05 | 成都施贝康生物医药科技有限公司 | 一种氧代吡啶类化合物的制备方法及中间体和应用 |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2396079A1 (en) | 2000-01-07 | 2001-07-19 | Transform Pharmaceuticals, Inc. | High-throughput formation, identification, and analysis of diverse solid-forms |
TWI633089B (zh) | 2013-03-28 | 2018-08-21 | 拜耳製藥股份有限公司 | 經取代的酮基吡啶衍生物 |
JO3703B1 (ar) * | 2015-07-09 | 2021-01-31 | Bayer Pharma AG | مشتقات أوكسوبيريدين مستبدلة |
CN107793396B (zh) | 2016-08-31 | 2021-02-26 | 江苏恒瑞医药股份有限公司 | 环氧基取代的氧代吡啶类衍生物、其制备方法及其在医药上的应用 |
EP3898611A1 (en) * | 2018-12-17 | 2021-10-27 | Bayer Aktiengesellschaft | Substituted oxopyridine derivatives for the treatment and/or prophylaxis of thrombotic or thromboembolic disorders and/or thrombotic or thromboembolic complications |
EP3898634A1 (en) * | 2018-12-21 | 2021-10-27 | Bayer Aktiengesellschaft | Substituted oxopyridine derivatives |
MA54521A (fr) * | 2018-12-21 | 2022-03-30 | Bayer Ag | Dérivés d'oxopyridine substitués |
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2019
- 2019-03-08 CN CN201980016087.2A patent/CN111770917B/zh active Active
- 2019-03-08 HR HRP20220565TT patent/HRP20220565T1/hr unknown
- 2019-03-08 JP JP2020548726A patent/JP7287978B2/ja active Active
- 2019-03-08 RS RS20220611A patent/RS63338B1/sr unknown
- 2019-03-08 IL IL300463A patent/IL300463A/en unknown
- 2019-03-08 JO JOP/2020/0232A patent/JOP20200232B1/ar active
- 2019-03-08 KR KR1020207026104A patent/KR20200131241A/ko unknown
- 2019-03-08 MX MX2020009580A patent/MX2020009580A/es unknown
- 2019-03-08 UA UAA202006635A patent/UA126940C2/uk unknown
- 2019-03-08 PE PE2020001408A patent/PE20211395A1/es unknown
- 2019-03-08 ES ES19708556T patent/ES2920449T3/es active Active
- 2019-03-08 CA CA3093733A patent/CA3093733A1/en active Pending
- 2019-03-08 DK DK19708556.6T patent/DK3765452T3/da active
- 2019-03-08 BR BR112020018562-0A patent/BR112020018562A2/pt unknown
- 2019-03-08 EP EP21169162.1A patent/EP3889147A1/en not_active Withdrawn
- 2019-03-08 SG SG11202006710RA patent/SG11202006710RA/en unknown
- 2019-03-08 WO PCT/EP2019/055815 patent/WO2019175043A1/en active Application Filing
- 2019-03-08 SI SI201930224T patent/SI3765452T1/sl unknown
- 2019-03-08 IL IL277240A patent/IL277240B2/en unknown
- 2019-03-08 PT PT197085566T patent/PT3765452T/pt unknown
- 2019-03-08 HU HUE19708556A patent/HUE058796T2/hu unknown
- 2019-03-08 AU AU2019236369A patent/AU2019236369B2/en active Active
- 2019-03-08 PL PL19708556.6T patent/PL3765452T3/pl unknown
- 2019-03-08 EP EP19708556.6A patent/EP3765452B1/en active Active
- 2019-03-08 US US16/980,210 patent/US11542245B2/en active Active
- 2019-03-08 LT LTEPPCT/EP2019/055815T patent/LT3765452T/lt unknown
- 2019-03-13 TW TW108108373A patent/TWI823911B/zh active
- 2019-03-15 AR ARP190100659A patent/AR117400A1/es unknown
- 2019-03-15 UY UY38147A patent/UY38147A/es unknown
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2020
- 2020-09-14 CL CL2020002371A patent/CL2020002371A1/es unknown
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