PL404112A1 - 3-Arylo-2-fosforylo podstawione indanony i sposób ich wytwarzania - Google Patents
3-Arylo-2-fosforylo podstawione indanony i sposób ich wytwarzaniaInfo
- Publication number
- PL404112A1 PL404112A1 PL404112A PL40411213A PL404112A1 PL 404112 A1 PL404112 A1 PL 404112A1 PL 404112 A PL404112 A PL 404112A PL 40411213 A PL40411213 A PL 40411213A PL 404112 A1 PL404112 A1 PL 404112A1
- Authority
- PL
- Poland
- Prior art keywords
- substituted
- unsubstituted
- aryl
- group
- preferably selected
- Prior art date
Links
- QNXSIUBBGPHDDE-UHFFFAOYSA-N indan-1-one Chemical class C1=CC=C2C(=O)CCC2=C1 QNXSIUBBGPHDDE-UHFFFAOYSA-N 0.000 title abstract 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 abstract 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 abstract 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 2
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 abstract 2
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 abstract 2
- 125000001072 heteroaryl group Chemical group 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- BBEAQIROQSPTKN-UHFFFAOYSA-N pyrene Chemical compound C1=CC=C2C=CC3=CC=CC4=CC=C1C2=C43 BBEAQIROQSPTKN-UHFFFAOYSA-N 0.000 abstract 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 abstract 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 abstract 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 abstract 1
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 abstract 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- GVEPBJHOBDJJJI-UHFFFAOYSA-N fluoranthrene Natural products C1=CC(C2=CC=CC=C22)=C3C2=CC=CC3=C1 GVEPBJHOBDJJJI-UHFFFAOYSA-N 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 239000011777 magnesium Substances 0.000 abstract 1
- 229910052749 magnesium Inorganic materials 0.000 abstract 1
- 229910052751 metal Inorganic materials 0.000 abstract 1
- 239000002184 metal Substances 0.000 abstract 1
- 229910052700 potassium Inorganic materials 0.000 abstract 1
- 239000011591 potassium Substances 0.000 abstract 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 abstract 1
- 229910052708 sodium Inorganic materials 0.000 abstract 1
- 239000011734 sodium Substances 0.000 abstract 1
- 229930192474 thiophene Natural products 0.000 abstract 1
- 229910052725 zinc Inorganic materials 0.000 abstract 1
- 239000011701 zinc Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/655—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having oxygen atoms, with or without sulfur, selenium, or tellurium atoms, as the only ring hetero atoms
- C07F9/65515—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having oxygen atoms, with or without sulfur, selenium, or tellurium atoms, as the only ring hetero atoms the oxygen atom being part of a five-membered ring
- C07F9/65517—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having oxygen atoms, with or without sulfur, selenium, or tellurium atoms, as the only ring hetero atoms the oxygen atom being part of a five-membered ring condensed with carbocyclic rings or carbocyclic ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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)
- Molecular Biology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biochemistry (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyrrole Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Przedmiotem wynalazku są 3-arylo-2-fosforylo podstawione 1-indanony i ich pochodne o wzorze ogólnym 1, w którym: R1 i R2 są takie same lub różne i oznaczają atomy wodoru; metalu, korzystnie sodu, potasu, magnezu i cynku lub grupę alkilową zawierającą 1-10 atomów węgla, R3 - oznacza atom wodoru, atom halogenu, a ArI i ArII - są takie same lub różne i oznaczają pierścień aromatyczny, podstawiony lub niepodstawiony, korzystnie wybrany z grupy obejmującej benzen, naftalen, piren; lub pierścień heteroaromatyczny sześcioczłonowy, podstawiony lub niepodstawiony, korzystnie wybrany z grupy obejmującej pirydynę, pirymidynę; lub pierścień hetero aromatyczny, pięcioczłonowy, podstawiony lub niepodstawiony, korzystnie wybrany z grupy obejmującej tiofen, pirol, furan. Wynalazek ujawnia też metodę wytwarzania tych pochodnych.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PL404112A PL223918B1 (pl) | 2013-05-28 | 2013-05-28 | 3-Arylo-2-fosforylo podstawione 1-indanony i sposób ich wytwarzania |
| EP14150858.0A EP2808337A1 (en) | 2013-05-28 | 2014-01-12 | (E)-3-Aryl-3-oxoprop-1-enyl-2-phosphonic acid and its derivatives, methods for their preparation and their use |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PL404112A PL223918B1 (pl) | 2013-05-28 | 2013-05-28 | 3-Arylo-2-fosforylo podstawione 1-indanony i sposób ich wytwarzania |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| PL404112A1 true PL404112A1 (pl) | 2014-12-08 |
| PL223918B1 PL223918B1 (pl) | 2016-11-30 |
Family
ID=49918585
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL404112A PL223918B1 (pl) | 2013-05-28 | 2013-05-28 | 3-Arylo-2-fosforylo podstawione 1-indanony i sposób ich wytwarzania |
Country Status (2)
| Country | Link |
|---|---|
| EP (1) | EP2808337A1 (pl) |
| PL (1) | PL223918B1 (pl) |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3337337A (en) | 1965-12-16 | 1967-08-22 | John W Weeton | Method for producing fiber reinforced metallic composites |
| KR940003548U (ko) | 1992-08-14 | 1994-02-21 | 김형술 | 세탁물 건조기 |
| US6447724B1 (en) | 1998-08-11 | 2002-09-10 | Caliper Technologies Corp. | DNA sequencing using multiple fluorescent labels being distinguishable by their decay times |
| WO2002045707A2 (en) | 2000-12-06 | 2002-06-13 | Lyles Mark B | Polynucleotide intercalator interceptors and inhibitors |
| US7306809B2 (en) | 2002-09-13 | 2007-12-11 | Lipo Chemicals, Inc. | Optically activated particles for use in cosmetic compositions |
| US8969027B2 (en) | 2008-03-03 | 2015-03-03 | Kansas State University Research Foundation | Protease assay |
| CA2658520C (en) | 2008-03-19 | 2016-11-08 | F. Hoffmann-La Roche Ag | Nucleic acid amplification in the presence of modified randomers |
| CN102014967A (zh) | 2008-03-21 | 2011-04-13 | 阿德利夫股份有限公司 | 芘携带肽穿过血脑屏障的用途 |
| EP2342340A1 (en) | 2008-09-22 | 2011-07-13 | Rxi Pharmaceuticals Corporation | Rna interference in skin indications |
| US8268977B2 (en) | 2008-11-20 | 2012-09-18 | The Board Of Trustees Of The Leland Stanford Junior University | Strongly quenching oligomeric excimer/quencher pairs for detection schemes |
| WO2012055409A1 (en) | 2010-10-27 | 2012-05-03 | Quantibact A/S | Capture of methylated rna and/or dna sequences by specific probes |
| KR20130113476A (ko) | 2010-10-27 | 2013-10-15 | ?티백트 에이/에스 | 인터칼레이터 （ｉｎｔｅｒｃａｌａｔｏｒ） 분자를 포함하는 프로브에 의한 표적 ＤＮＡ 및 ＲＮＡ의 캡쳐 |
-
2013
- 2013-05-28 PL PL404112A patent/PL223918B1/pl unknown
-
2014
- 2014-01-12 EP EP14150858.0A patent/EP2808337A1/en not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| EP2808337A1 (en) | 2014-12-03 |
| PL223918B1 (pl) | 2016-11-30 |
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