ES2608871T3 - Alafenamide hemifumarate de tenofovir - Google Patents

Alafenamide hemifumarate de tenofovir Download PDF

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Publication number
ES2608871T3
ES2608871T3 ES12753867.6T ES12753867T ES2608871T3 ES 2608871 T3 ES2608871 T3 ES 2608871T3 ES 12753867 T ES12753867 T ES 12753867T ES 2608871 T3 ES2608871 T3 ES 2608871T3
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tenofovir alafenamide
tenofovir
hemifumarate
alafenamide
monofumate
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ES2608871T5 (es
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Dazhan LIU
Bing Shi
Fang Wang
Richard Hung Chiu Yu
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Gilead Sciences Inc
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Gilead Sciences Inc
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/547Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/6561Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings
    • C07F9/65616Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings containing the ring system having three or more than three double bonds between ring members or between ring members and non-ring members, e.g. purine or analogs
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/547Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/6561Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings
    • 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
    • A61K31/495Heterocyclic 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • A61K31/52Purines, e.g. adenine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/66Phosphorus compounds
    • A61K31/683Diesters of a phosphorus acid with two hydroxy compounds, e.g. phosphatidylinositols
    • A61K31/685Diesters of a phosphorus acid with two hydroxy compounds, e.g. phosphatidylinositols one of the hydroxy compounds having nitrogen atoms, e.g. phosphatidylserine, lecithin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/14Antivirals for RNA viruses
    • A61P31/18Antivirals for RNA viruses for HIV
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/20Antivirals for DNA viruses
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D473/00Heterocyclic compounds containing purine ring systems
    • C07D473/26Heterocyclic compounds containing purine ring systems with an oxygen, sulphur, or nitrogen atom directly attached in position 2 or 6, but not in both
    • C07D473/32Nitrogen atom
    • C07D473/34Nitrogen atom attached in position 6, e.g. adenine

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Molecular Biology (AREA)
  • Virology (AREA)
  • Epidemiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oncology (AREA)
  • Communicable Diseases (AREA)
  • Biochemistry (AREA)
  • AIDS & HIV (AREA)
  • Biotechnology (AREA)
  • Engineering & Computer Science (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Medicinal Preparation (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Peptides Or Proteins (AREA)

Abstract

Hemifumarato de tenofovir alafenamida.

Description

imagen1
imagen2
imagen3
imagen4
imagen5
imagen6
imagen7
Datos TGA
[0062] Los datos de TGA se obtuvieron usando 4,161 mg de hemifumarato de tenofovir alafenamida. Se calentó a 10ºC/min en el intervalo de 25-200ºC. La muestra perdió 0,3% de peso antes de la fusión (Fig. 3). Se determinó que es una forma anhidra.
Análisis DVS
[0063] El análisis DVS se realizó utilizando 4,951 mg de hemifumarato de tenofovir alafenamida. El material se mantuvo a 25ºC en nitrógeno a humedades comprendidas entre 10% y 90% de humedad relativa; Cada etapa se equilibró durante 120 minutos. La isoterma de adsorción se muestra en la FIG. 4. Se demostró que el material era no higroscópico, y absorbía 0,65% de agua a una humedad relativa de 90%.
Purga de la impureza diastereomérica
[0064] En las síntesis anteriores de tenofovir alafenamida, una de las principales impurezas es típicamente el diastereómero 9-[(R)-2-[[(R)-[[(S)-1-(isopropoxicarbonilo)etilo]amino]fenoxifosfinilo]metoxi]propilo]adenina. La forma de hemifumarato de tenofovir alafenamida del Ejemplo 3 tiene una capacidad excepcional para purgar esta impureza diastereomérica, en comparación con la capacidad de la forma de monofumarato (descrita en la Patente de Estados Unidos nº 7.390.791). Los datos de la Tabla 2 (a continuación) demuestran que el hemifumarato de tenofovir alafenamida (Lote 2) purgó la impureza diastereomérica a menos de una décima parte de la concentración inicial, mientras que la forma de monofumarato de tenofovir alafenamida (Lote 1) sólo purgó ligeramente la impureza diastereomérica.
Tabla 2. Comparación de capacidades de purga
Lote
La impureza diastereomérica en material de partida Solvente Carga de ácido fumárico (equivalente molar) Producto obtenido La impureza diastereomérica de producto
1
9,3% ACN 0,9 Forma de monofumarato 7,6%
2
10,0% ACN 0,5 Forma de hemifumarato 0,65%
Estabilidad química
[0065] La estabilidad química de la forma de hemifumarato de tenofovir alafenamida se comparó con la forma de monofumarato. Como se muestra en la Tabla 3 (a continuación), en condiciones idénticas, la forma de hemifumarato de tenofovir alafenamida era químicamente más estable y exhibe una mejor estabilidad de almacenamiento a largo plazo, con significativamente menos degradación (% Deg Total. Productos) que la forma de monofumarato. Condiciones evaluadas incluyen la temperatura, la humedad relativa (RH), y el estado abierto o cerrado de la tapa del recipiente.
Tabla 3. Estabilidad química Comparación
Condición de almacenamiento
Puntos de tiempo (semanas) Forma de monofumarato Forma de hemifumarato
% TA* Área normalizada
% Total Deg. Productos % TA área normalizada Total% Deg. Productos
40°C/75% RH tapa cerrada
0 97,1 0,69 98,4 0,05
1
97,0 0,87 98,4 0,14
2
96,6 1,18 98,5 0,14
4
96,4 1,49 98,4 0,25
8
95,4 2,36 98,0 0,49
40°C/75% RH tapa abierta
0 97,1 0,69 98,4 0,05
1
96,9 0,90 98,5 0,15
2
96,6 1,10 98,5 0,14
4
96,2 1,67 98,4 0,26
8
95,0 2,74 98,1 0,50
70°C tapa cerrada
0 97,1 0,69 98,4 0,05
2
96,2 1,83 98,5 0,22
4
93,3 4,78 98,4 0,33
TA es tenofovir alafenamida
imagen8

Claims (1)

  1. imagen1
ES12753867T 2011-08-16 2012-08-15 Alafenamide hemifumarate de tenofovir Active ES2608871T5 (es)

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US201161524224P 2011-08-16 2011-08-16
US201161524224P 2011-08-16
PCT/US2012/050920 WO2013025788A1 (en) 2011-08-16 2012-08-15 Tenofovir alafenamide hemifumarate

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