DK2714710T3 - Fremgangsmåde til fremstilling af estetrol-mellemprodukter - Google Patents

Fremgangsmåde til fremstilling af estetrol-mellemprodukter Download PDF

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Publication number
DK2714710T3
DK2714710T3 DK12729054.2T DK12729054T DK2714710T3 DK 2714710 T3 DK2714710 T3 DK 2714710T3 DK 12729054 T DK12729054 T DK 12729054T DK 2714710 T3 DK2714710 T3 DK 2714710T3
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formula
compound
group
process according
alkyl
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DK12729054.2T
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Jean-Claude Pascal
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Estetra Sprl
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P5/00Drugs for disorders of the endocrine system
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J75/00Processes for the preparation of steroids in general
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J1/00Normal steroids containing carbon, hydrogen, halogen or oxygen, not substituted in position 17 beta by a carbon atom, e.g. estrane, androstane
    • C07J1/0051Estrane derivatives
    • C07J1/0066Estrane derivatives substituted in position 17 beta not substituted in position 17 alfa
    • C07J1/007Estrane derivatives substituted in position 17 beta not substituted in position 17 alfa the substituent being an OH group free esterified or etherified
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J1/00Normal steroids containing carbon, hydrogen, halogen or oxygen, not substituted in position 17 beta by a carbon atom, e.g. estrane, androstane
    • C07J1/0051Estrane derivatives
    • C07J1/0066Estrane derivatives substituted in position 17 beta not substituted in position 17 alfa
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/56Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
    • A61K31/565Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids not substituted in position 17 beta by a carbon atom, e.g. estrane, estradiol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P5/00Drugs for disorders of the endocrine system
    • A61P5/24Drugs for disorders of the endocrine system of the sex hormones
    • A61P5/30Oestrogens
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J1/00Normal steroids containing carbon, hydrogen, halogen or oxygen, not substituted in position 17 beta by a carbon atom, e.g. estrane, androstane
    • C07J1/0051Estrane derivatives
    • C07J1/0059Estrane derivatives substituted in position 17 by a keto group
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J13/00Normal steroids containing carbon, hydrogen, halogen or oxygen having a carbon-to-carbon double bond from or to position 17
    • C07J13/005Normal steroids containing carbon, hydrogen, halogen or oxygen having a carbon-to-carbon double bond from or to position 17 with double bond in position 16 (17)
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J51/00Normal steroids with unmodified cyclopenta(a)hydrophenanthrene skeleton not provided for in groups C07J1/00 - C07J43/00
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/55Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Endocrinology (AREA)
  • Engineering & Computer Science (AREA)
  • Diabetes (AREA)
  • Epidemiology (AREA)
  • Steroid Compounds (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)

Claims (14)

1. Fremgangsmåde til fremstilling af en forbindelse med formel (I)
(I) hvilken fremgangsmåde omfatter følgende trin a) omsætning af en forbindelse med formel (II) med et acylerings- eller et sily-leringsmiddel til dannelse af en forbindelse med formel (III), hvor P1 og P2 hver især uafhængigt er en beskyttelsesgruppe, som er valgt blandt R2-Si-R3R4 eller R1CO-, hvor R1 er en gruppe, som er valgt blandt Ci_6alkyl eller C3-6cycloalkyl, idet hver gruppe eventuelt er substitueret med én eller flere substituenter, som uafhængigt er valgt blandt fluor eller Ci^alkyl; R2, R3 og R4 hver især uafhængigt er en gruppe, som er valgt blandt Ci_6alkyl eller phenyl, idet hver gruppe eventuelt er substitueret med én eller flere substituenter, som uafhængigt er valgt blandt fluor eller Ci^alkyl;
(II) (III) b) omsætning af forbindelsen med formel (III) i nærværelse af palladiumacetat eller palladiumchlorid til dannelse af en forbindelse med formel (IV); og
(IV) c) omsætning af forbindelsen med formel (IV) med et reduktionsmiddel til dannelse af en forbindelse med formel (I).
2. Fremgangsmåde ifølge krav 1, hvor P1 er R1CO-.
3. Fremgangsmåde ifølge krav 1, hvor P1 er R2-Si-R3R4.
4. Fremgangsmåde ifølge krav 3, hvor P2 er R2-Si-R3R4.
5. Fremgangsmåde ifølge et hvilket som helst af kravene 1 til 3, hvor P2 er R1CO-.
6. Fremgangsmåde ifølge krav 5, hvor trin (a) omfatter følgende trin: (a1) beskyttelse af hydroxyl i en forbindelse med formel (II) med et silyleringsmiddel til dannelse af en forbindelse med formel (Ila), hvor P1 harden samme betydning som defineret i krav 3; og
(Ila) (a2) beskyttelse af ketonen i en forbindelse med formel (Ila) i nærværelse af et acyle-ringsmiddel til dannelse af en forbindelse med formel (III).
7. Fremgangsmåde ifølge et hvilket som helst af kravene 1 til 3, 5 og 6, hvor acyle-ringsmidlet er C2-6alkenylCi-6alkanoat eller C2-6alkenylC3-6cycloalkanoat.
8. Fremgangsmåde ifølge et hvilket som helst af kravene 1,3 til 7, hvor silyleringsmid-let er valgt fra gruppen omfattende Ci-6alkylsilylchlorid, Ci-6alkylsilyltriflat, phenylsilyl-chlorid, phenylsilyltriflat, Ci-6alkylphenylsilylchlorid, Ci-6alkylphenylsilyltriflat, idet hver gruppe eventuelt er substitueret med én eller flere substituenter, som uafhængigt er valgt blandt fluor eller Ci.4alkyl.
9. Fremgangsmåde ifølge et hvilket som helst af kravene 1 til 8, hvor trin (b) udføres i nærværelse af et Ci.6alkylencarbonat med formel Rb-0-C0-0-Ra, hvor Ra er Ci.6-alkyl, og Rb er C2.6-alkenyl, og en organotinforbindelse.
10. Fremgangsmåde ifølge et hvilket som helst af kravene 1 til 9, hvor palladiumacetatet eller palladiumchloridet er til stede i støkiometriske mængder.
11. Fremgangsmåde ifølge et hvilket som helst af kravene 1 til 9, hvor reaktionen udføres med palladiumacetat eller palladiumchlorid, som er til stede i katalytiske eller sub-støkiometriske mængder, idet reaktionen fortrinsvis udføres i en oxygenatmosfære.
12. Fremgangsmåde ifølge et hvilket som helst af kravene 1 til 11, hvor reduktionsmidlet i trin (c) er valgt fra gruppen af metalhydridforbindelser.
13. Fremgangsmåde ifølge krav 12, hvor metalhydridforbindelsen er valgt fra gruppen omfattende NaBH4/CeCI3, LiAIH4, NaBH4, NaBH(OAc)3 og ZnBH4.
14. Fremgangsmåde til fremstilling af estetrol, hvilken fremgangsmåde omfatter fremstilling af en forbindelse med formel (I) ved en fremgangsmåde ifølge et hvilket som helst af kravene 1 til 13 og yderligere omsætning af en forbindelse med formel (I) til dannelse af estetrol.
DK12729054.2T 2011-06-01 2012-06-01 Fremgangsmåde til fremstilling af estetrol-mellemprodukter DK2714710T3 (da)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201161492300P 2011-06-01 2011-06-01
EP11168561 2011-06-01
PCT/EP2012/060447 WO2012164096A1 (en) 2011-06-01 2012-06-01 Process for the production of estetrol intermediates

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DK2714710T3 true DK2714710T3 (da) 2016-06-27

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US (1) US11053274B2 (da)
EP (1) EP2714710B1 (da)
JP (2) JP6425540B2 (da)
KR (1) KR101994805B1 (da)
CN (2) CN103703014A (da)
AU (1) AU2012264602B2 (da)
BR (1) BR112013030830B1 (da)
CA (1) CA2835981C (da)
CY (1) CY1118150T1 (da)
DK (1) DK2714710T3 (da)
EA (1) EA023991B1 (da)
ES (1) ES2579175T3 (da)
HR (1) HRP20160692T2 (da)
HU (1) HUE029252T2 (da)
ME (1) ME02454B (da)
MX (1) MX341561B (da)
PL (1) PL2714710T3 (da)
PT (1) PT2714710T (da)
RS (1) RS54880B1 (da)
SG (1) SG195118A1 (da)
SI (1) SI2714710T1 (da)
SM (1) SMT201600206B (da)
WO (1) WO2012164096A1 (da)
ZA (1) ZA201308446B (da)

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