PL438192A1 - Pochodna naproksenu i sposób wytwarzania pochodnej naproksenu - Google Patents

Pochodna naproksenu i sposób wytwarzania pochodnej naproksenu

Info

Publication number
PL438192A1
PL438192A1 PL438192A PL43819221A PL438192A1 PL 438192 A1 PL438192 A1 PL 438192A1 PL 438192 A PL438192 A PL 438192A PL 43819221 A PL43819221 A PL 43819221A PL 438192 A1 PL438192 A1 PL 438192A1
Authority
PL
Poland
Prior art keywords
naproxen
derivative
methoxynaphthalen
amino acid
producing
Prior art date
Application number
PL438192A
Other languages
English (en)
Inventor
Ewa Janus
Paula Ossowicz-Rupniewska
Ewelina Świątek
Original Assignee
Zachodniopomorski Uniwersytet Technologiczny W Szczecinie
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Zachodniopomorski Uniwersytet Technologiczny W Szczecinie filed Critical Zachodniopomorski Uniwersytet Technologiczny W Szczecinie
Priority to PL438192A priority Critical patent/PL438192A1/pl
Publication of PL438192A1 publication Critical patent/PL438192A1/pl

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D207/00Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/04Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D207/10Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members 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
    • C07D207/16Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/185Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • A61K31/19Carboxylic acids, e.g. valproic acid
    • A61K31/192Carboxylic acids, e.g. valproic acid having aromatic groups, e.g. sulindac, 2-aryl-propionic acids, ethacrynic acid 
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/401Proline; Derivatives thereof, e.g. captopril
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/41Preparation of salts of carboxylic acids
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/42Separation; Purification; Stabilisation; Use of additives
    • C07C51/43Separation; Purification; Stabilisation; Use of additives by change of the physical state, e.g. crystallisation
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C59/00Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
    • C07C59/40Unsaturated compounds
    • C07C59/58Unsaturated compounds containing ether groups, groups, groups, or groups
    • C07C59/64Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Epidemiology (AREA)
  • Engineering & Computer Science (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Przedmiotem zgłoszenia jest pochodna naproksenu, która charakteryzuje się tym, że ma postać soli organicznej o wzorze, w której kation jest pochodzenia aminokwasowego i stanowi pochodną aminokwasu w postaci estru etylowego, izopropylowego, propylowego i butylowego L-proliny i ma anion (2S)-2-(6-metoksynaftalen-2-ylo)propanianowy Zgłoszenie obejmuje też sposób wytwarzania pochodnej naproksenu, według wynalazku, polegający na reakcji estru alkilowego aminokwasu z kwasem (2S)-2-(6-metoksynaftalen-2-ylo)propanowym w ilości stechiometrycznej, charakteryzuje się tym, że do kwasu metoksynaftalen-2-ylo)propanowego dodaje się ester etylowy, izopropylowy, propylowy lub butylowy L-proliny, a reakcję protonowania estru kwasem prowadzi się w środowisku bezrozpuszczalnikowym w temperaturze pokojowej, w czasie 5 - 45 minut.
PL438192A 2021-06-18 2021-06-18 Pochodna naproksenu i sposób wytwarzania pochodnej naproksenu PL438192A1 (pl)

Priority Applications (1)

Application Number Priority Date Filing Date Title
PL438192A PL438192A1 (pl) 2021-06-18 2021-06-18 Pochodna naproksenu i sposób wytwarzania pochodnej naproksenu

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PL438192A PL438192A1 (pl) 2021-06-18 2021-06-18 Pochodna naproksenu i sposób wytwarzania pochodnej naproksenu

Publications (1)

Publication Number Publication Date
PL438192A1 true PL438192A1 (pl) 2022-12-19

Family

ID=84487965

Family Applications (1)

Application Number Title Priority Date Filing Date
PL438192A PL438192A1 (pl) 2021-06-18 2021-06-18 Pochodna naproksenu i sposób wytwarzania pochodnej naproksenu

Country Status (1)

Country Link
PL (1) PL438192A1 (pl)

Similar Documents

Publication Publication Date Title
MX2024008497A (es) Fabricacion de compuestos y composiciones para inhibir la actividad de shp2.
BR112012030923B8 (pt) Composto derivado de piperidinona como inibidor de mdm2 e composição farmacêutica compreendendo o mesmo
MX353957B (es) Carboxamidas heterociclicas fungicidas.
RU2013156980A (ru) Соединения и композиции для стабилизации индуцируемого гипоксией фактора-2 альфа как способ лечения рака
MY157327A (en) Fungicidal pyrazoles and their mixtures
UA96450C2 (ru) Азолилметилоксираны, их применение для борьбы с фитопатогенными грибами, средство для защиты растений, способ борьбы с фитопатогенными грибами и посевной материал
PH12014501732A1 (en) Fungicidal pyrazole mixtures
EA201400137A1 (ru) Фунгицидные алкилзамещенные 2-[2-хлоро-4-(4-хлорофенокси)фенил]-1-[1,2,4]триазол-1-ил-этанольные соединения
MX2013006926A (es) Compuestos y composiciones fotocromicas.
NO20091664L (no) Farmaoytiske preparater av HDAC-inhibitorer og chelaterbare metallforbindelser samt metall-HDAC-inhibitor-chelatkomplekser
JP2007532525A (ja) 液体
JP2010528155A5 (pl)
EA201400234A1 (ru) Фунгицидные замещенные 1-{2-[2-галоген-4(4-галогенфенокси)фенил]-2-алкинилоксиэтил}-1н-[1,2,4]триазолные соединения
GB201100181D0 (en) Fused aminodihydrothiazine derivatives
AR069437A1 (es) Bisfosfonatos de alquilo de 2 a 5 atomos de carbono - imidazol
IN2014CN02188A (pl)
EA200701162A1 (ru) Четвертичные аммониевые соли, как конверсионные покрытия или противокоррозионная добавка для красок
IN2014CN03646A (pl)
PL438192A1 (pl) Pochodna naproksenu i sposób wytwarzania pochodnej naproksenu
WO2021256448A1 (ja) 潤滑性を付与する添加剤又は組成物
PH12021551495A1 (en) Crystalline and salt forms of an organic compound and pharmaceutical compositions thereof
MX2010013758A (es) Procedimiento para elaborar 2-amino-tiazolonas sustituidas.
NZ611965A (en) Synthesis and novel salt forms of (r)-5-((e)-2-(pyrrolidin-3-ylvinyl)pyrimidine
EA201590818A1 (ru) Замещенные триазолы в качестве гербицидов
WO2007061966A3 (en) Amidinylphenyl compounds and their use as fungicides