AR087875A1 - PROCESS FOR THE ELABORATION OF PIRIDAZINE DERIVATIVES AS ANTIBIOTICS SYNTHESIS INTERMEDIARIES - Google Patents
PROCESS FOR THE ELABORATION OF PIRIDAZINE DERIVATIVES AS ANTIBIOTICS SYNTHESIS INTERMEDIARIESInfo
- Publication number
- AR087875A1 AR087875A1 ARP120103393A ARP120103393A AR087875A1 AR 087875 A1 AR087875 A1 AR 087875A1 AR P120103393 A ARP120103393 A AR P120103393A AR P120103393 A ARP120103393 A AR P120103393A AR 087875 A1 AR087875 A1 AR 087875A1
- Authority
- AR
- Argentina
- Prior art keywords
- compound
- oxatiino
- pyridazin
- dihydro
- formula
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D497/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having oxygen and sulfur atoms as the only ring hetero atoms
- C07D497/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having oxygen and sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D497/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Un intermediario de síntesis utilizado comúnmente en la preparación de compuestos antibióticos, o para la elaboración de sales de ese compuesto. La presente se relaciona asimismo con compuestos intermedios utilizados en dicho proceso, es decir 6,7-dihidro-[1,4]oxatiino[2,3-c]piridazin-3(2H)-ona, trifluorometansulfonato de 6,7-dihidro-[1,4]oxatiino[2 ,3-c]piridazin-3-ilo y 6,7-dihidro-[1,4]oxatiino[2,3-c]piridazin-3-carboxilato de metilo y con las sales del mismo. Reivindicación 1: El compuesto de la fórmula (1) o una sal de dicho compuesto. Reivindicación 2: Un proceso para la elaboración del compuesto de la fórmula (1) de acuerdo con lo definido en la reivindicación 1, donde dicho proceso comprende los siguientes dos pasos: a) la reacción del compuesto de la fórmula (2) con 2-mercaptoetanol en presencia de una base en un solvente aprótico polar o una mezcla aprótica polar de solventes y b) la reacción del intermediario obtenido después del paso a) anterior con trifenilfosfina y azodicarboxilato de diisopropilo o azodicarboxilato de dietilo en un solvente aprótico polar o una mezcla aprótica polar de solventes.A synthesis intermediate commonly used in the preparation of antibiotic compounds, or for the preparation of salts of that compound. This also relates to intermediate compounds used in said process, that is 6,7-dihydro- [1,4] oxatiino [2,3-c] pyridazin-3 (2H) -one, 6,7-dihydro trifluoromethanesulfonate - [1,4] oxatiino [2,3-c] pyridazin-3-yl and 6,7-dihydro- [1,4] oxatiino [2,3-c] pyridazin-3-carboxylic acid methyl ester and with salts of the same. Claim 1: The compound of the formula (1) or a salt of said compound. Claim 2: A process for the preparation of the compound of the formula (1) as defined in claim 1, wherein said process comprises the following two steps: a) the reaction of the compound of the formula (2) with 2- mercaptoethanol in the presence of a base in a polar aprotic solvent or a polar aprotic solvent mixture and b) the reaction of the intermediate obtained after step a) above with triphenylphosphine and diisopropyl azodicarboxylate or diethyl azodicarboxylate in a polar aprotic solvent or an aprotic mixture polar of solvents.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IB2011054061 | 2011-09-16 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR087875A1 true AR087875A1 (en) | 2014-04-23 |
Family
ID=47080755
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP120103393A AR087875A1 (en) | 2011-09-16 | 2012-09-14 | PROCESS FOR THE ELABORATION OF PIRIDAZINE DERIVATIVES AS ANTIBIOTICS SYNTHESIS INTERMEDIARIES |
Country Status (3)
Country | Link |
---|---|
AR (1) | AR087875A1 (en) |
TW (1) | TW201313726A (en) |
WO (1) | WO2013038374A1 (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP7413346B2 (en) | 2019-03-06 | 2024-01-15 | 第一三共株式会社 | Pyrrolopyrazole derivative |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
PT1954697E (en) | 2005-10-21 | 2010-05-17 | Glaxo Group Ltd | Peri condensed tricyclic compounds useful as antibacterial agents |
JP2009520779A (en) | 2005-12-22 | 2009-05-28 | グラクソ グループ リミテッド | Heterocyclic compounds, their production and their use as antibacterial agents |
GB0613208D0 (en) | 2006-07-03 | 2006-08-09 | Glaxo Group Ltd | Compounds |
EP1992628A1 (en) | 2007-05-18 | 2008-11-19 | Glaxo Group Limited | Derivatives and analogs of N-ethylquinolones and N-ethylazaquinolones |
GB0705672D0 (en) | 2007-03-23 | 2007-05-02 | Glaxo Group Ltd | Compounds |
EP1980251A1 (en) | 2007-04-13 | 2008-10-15 | Glaxo Group Limited | Pyrrolo[3,2,1-ij]quinoline-4-one derivatives for treating tuberculosis |
ES1065649Y (en) | 2007-06-22 | 2008-01-01 | Gavalda Josep Sarmiento | PERFECTED MOUTH OPENING PROVISION FOR ANIMALS |
WO2009128953A2 (en) | 2008-04-18 | 2009-10-22 | University Of Maryland, Baltimore | Genetic variants in a hypertension susceptibility gene stk39 and uses thereof |
MX2011005905A (en) | 2008-12-12 | 2011-06-20 | Actelion Pharmaceuticals Ltd | 5-amino-2-(1-hydroxy-ethyl)-tetrahydropyran derivatives. |
AR076222A1 (en) | 2009-04-09 | 2011-05-26 | Actelion Pharmaceuticals Ltd | DERIVATIVES 2-HYDROXIETIL-1H-QUINOLIN-ONA AND ITS AZAISOTHERAL ANALOGS WITH ANTIBACTERIAL ACTIVITY AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM |
-
2012
- 2012-09-14 TW TW101133871A patent/TW201313726A/en unknown
- 2012-09-14 WO PCT/IB2012/054804 patent/WO2013038374A1/en active Application Filing
- 2012-09-14 AR ARP120103393A patent/AR087875A1/en not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
WO2013038374A1 (en) | 2013-03-21 |
TW201313726A (en) | 2013-04-01 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
UY34870A (en) | SALT CRYSTALS | |
UY36152A (en) | ADDITION SALTS OF (S) -2- (1- (6-AMINO-5-CYANOPIRIMIDIN-4-ILAMINO) ETIL) -4-OXO-3-PHENYL-3,4-DIHYDROPIRROLO [1,2-F] [ 1,2,4] TRIAZINE-5-CARBONITRILE | |
CR20130371A (en) | IMIDAZO [5,1-f] [1,2,4] TRIAZINS FOR THE TREATMENT OF NEUROLOGICAL DISORDERS | |
MX2013011854A (en) | Tri- and tetracyclic pyrazolo[3,4-b]pyridine compounds as antineoplastic agent. | |
CU20170160A7 (en) | DERIVADOSDE FENIL-TIENO (2,3-D) PIRIMIDINA- HIDROXI-ESTERES, A PROCESS FOR ITS PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING IT | |
EA201490831A1 (en) | METHOD OF OBTAINING QUINOLINE DERIVATIVES | |
EA201300620A1 (en) | Imidazo [1,2-b] derivatives of pyridazine and imidazo [4,5-b] pyridine as JAK inhibitors | |
CR20210055A (en) | Salts of pi3k inhibitor and processes for their preparation | |
ECSP14006132A (en) | BENZOTHIAZOLE-6-IL ACETIC ACID DERIVATIVES AND THEIR USE TO TREAT HIV INFECTION | |
HRP20160319T1 (en) | Synthesis of n4- (2, 2-dimethyl-4- [ (dihydrogen phosphonoxy]-3-oxo-5-pyrido [1, 4]oxazin-6-yl)-5-fluoro-n2- (3, 4, 5,-trimethoxyphenyl) -2, 4- pyrimidinediamine disodium salt | |
CU24272B1 (en) | TETRAHYDROPIRID-PYRIMIDINE DERIVATIVES AS MEK INHIBITORS | |
CR20130531A (en) | DERIVATIVES OF NUCLEOSIDS 2'-SUBSTITUTES AND METHODS OF USE OF THE SAME FOR THE TREATMENT OF VIRAL DISEASES | |
EA201591545A1 (en) | C-3 ALKYL AND ALKENYL-MODIFIED BETULINIC ACID DERIVATIVES | |
BR112015009395A2 (en) | process for preparation of bile acid derivatives | |
HRP20161031T1 (en) | METHODS FOR THE PREPARATION OF (3R,3aS,6aR) HEXAHYDRO-FURO[2,3-b]FURAN-3-OL | |
AR088326A1 (en) | SOLID FORMS OF NEMATOCID SULFONAMIDS | |
MX2013007148A (en) | 2-arylimidazo[1,2-b]pyridazine, 2-phenylimidazo[1,2-a]pyridine, and 2-phenylimidazo[1,2-a]pyrazine derivatives. | |
NZ605627A (en) | Pyrrolo-pyrazine derivatives useful as inhibitors of atr kinase | |
CO6400217A2 (en) | (1-PHENYL-2-PIRIDIN-4-IL) ETHYL ESTERS OF BENZOIC ACID AS PHOSPHODIESTERASE INHIBITORS | |
PE20171104A1 (en) | PYRAZOLE PYRIDINAMINES AS INHIBITORS OF MKNK1 AND MKNK2 | |
AR077924A1 (en) | PROCESSES TO PREPARE PEMETREXED | |
NI201500134A (en) | DERIVATIVES OF 2 - ((4-AMINO-3- (3-FLUORO-5-HYDROXYPHENIL) -1H-PIRAZOLO [3,4-D] PYRIMIDIN-1-IL) METHYL) -3- (2- (TRIFLUOROMETHYL) BENZYL ) QUINAZOLINE-4 (3H) -ONE AND ITS USE AS INHIBITORS OF PHOSPHOINOSITIDE 3-KINASES | |
CR20140133A (en) | PIRIDAZINONA COMPOUNDS AND THEIR USES AS DAAO INHIBITORS | |
AR075368A1 (en) | GLICOSILCERAMIDE SINTASA INHIBITORS | |
CO7141413A2 (en) | Process for the preparation of optically pure and optionally substituted 2- (1-hydroxy-alkyl) -chromen-4-one derivatives and their use in the preparation of pharmaceutical compounds |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FA | Abandonment or withdrawal |