MA39126A2 - Synthèse d'enantiomère de progestérone et d'intermédiaires de celui-ci - Google Patents

Synthèse d'enantiomère de progestérone et d'intermédiaires de celui-ci

Info

Publication number
MA39126A2
MA39126A2 MA39126A MA39126A MA39126A2 MA 39126 A2 MA39126 A2 MA 39126A2 MA 39126 A MA39126 A MA 39126A MA 39126 A MA39126 A MA 39126A MA 39126 A2 MA39126 A2 MA 39126A2
Authority
MA
Morocco
Prior art keywords
progesterone
intermediates
enantiomeric synthesis
enantiomeric
synthesis
Prior art date
Application number
MA39126A
Other languages
English (en)
Other versions
MA39126A3 (fr
MA39126B1 (fr
Inventor
Daniel Levy
Faliang Zhang
Xinxi Zhan
Original Assignee
Prevacus Inc
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 Prevacus Inc filed Critical Prevacus Inc
Publication of MA39126A2 publication Critical patent/MA39126A2/fr
Publication of MA39126A3 publication Critical patent/MA39126A3/fr
Publication of MA39126B1 publication Critical patent/MA39126B1/fr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D317/00Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
    • C07D317/08Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
    • C07D317/10Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings
    • C07D317/14Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D317/26Radicals substituted by doubly bound oxygen or sulfur atoms or by two such atoms singly bound to the same carbon atom
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00Drugs for genital or sexual disorders; Contraceptives
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D317/00Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
    • C07D317/08Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
    • C07D317/10Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings
    • C07D317/14Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D317/30Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D317/00Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
    • C07D317/08Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
    • C07D317/72Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 spiro-condensed with carbocyclic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J15/00Stereochemically pure steroids containing carbon, hydrogen, halogen or oxygen having a partially or totally inverted skeleton, e.g. retrosteroids, L-isomers
    • C07J15/005Retrosteroids (9 beta 10 alfa)
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J21/00Normal steroids containing carbon, hydrogen, halogen or oxygen having an oxygen-containing hetero ring spiro-condensed with the cyclopenta(a)hydrophenanthrene skeleton
    • C07J21/005Ketals
    • C07J21/006Ketals at position 3
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J75/00Processes for the preparation of steroids in general
    • C07J75/005Preparation of steroids by cyclization of non-steroid compounds

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Endocrinology (AREA)
  • Reproductive Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Steroid Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Physical Or Chemical Processes And Apparatus (AREA)
  • Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms (AREA)

Abstract

La présente invention concerne la synthèse d'enantiomère de progestérone et d'intermédiaires de celui-ci.
MA39126A 2013-12-20 2014-12-17 Synthèse d'enantiomère de progestérone et d'intermédiaires de celui-ci MA39126B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201361919420P 2013-12-20 2013-12-20
PCT/US2014/070879 WO2015095339A1 (fr) 2013-12-20 2014-12-17 Synthèse d'enantiomère de progestérone et d'intermédiaires de celui-ci

Publications (3)

Publication Number Publication Date
MA39126A2 true MA39126A2 (fr) 2018-08-31
MA39126A3 MA39126A3 (fr) 2019-04-30
MA39126B1 MA39126B1 (fr) 2020-03-31

Family

ID=53399300

Family Applications (1)

Application Number Title Priority Date Filing Date
MA39126A MA39126B1 (fr) 2013-12-20 2014-12-17 Synthèse d'enantiomère de progestérone et d'intermédiaires de celui-ci

Country Status (18)

Country Link
US (1) US20150175650A1 (fr)
EP (1) EP3083656A1 (fr)
JP (1) JP2017502031A (fr)
CN (1) CN105980396B (fr)
AR (1) AR098879A1 (fr)
AU (1) AU2014364850A1 (fr)
BR (1) BR112016014000A2 (fr)
CA (1) CA2934466A1 (fr)
EA (1) EA201691074A1 (fr)
IL (1) IL246258A0 (fr)
MA (1) MA39126B1 (fr)
MX (1) MX2016008167A (fr)
PH (1) PH12016501201A1 (fr)
SG (1) SG11201604982XA (fr)
TN (1) TN2016000252A1 (fr)
TW (1) TW201538519A (fr)
UY (1) UY35909A (fr)
WO (1) WO2015095339A1 (fr)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2017100988A (ja) * 2015-12-01 2017-06-08 アサヒグループホールディングス株式会社 光学活性なヒドロキシ脂肪酸の製造方法
IT201700004904A1 (it) * 2017-01-18 2018-07-18 Ind Chimica Srl PROCESSO PER LA PREPARAZIONE DI 9β,10α-PROGESTERONE (RETROPROGESTERONE)
US12503485B2 (en) 2019-08-02 2025-12-23 Enterin, Inc. Human aminosterol ENT-03 compounds, related compositions comprising the same, and methods of using the same
JP2022543244A (ja) * 2019-08-02 2022-10-11 エンターイン、 インコーポレイテッド ヒトスクアラミン誘導体、それを含む関連組成物、およびそれを用いた方法

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2716095C (fr) * 2008-02-26 2017-02-07 Emory University Analogues steroidiens utilises en neuroprotection
WO2010088409A2 (fr) * 2009-01-30 2010-08-05 Emory University Procédés de neuroprotection utilisant des stéroïdes neuroprotecteurs et une vitamine d
US8492368B2 (en) * 2011-10-07 2013-07-23 Florida State University Research Foundation Nasal delivery mechanism for prophylactic and post-acute use of progesterone and/or its enantiomer for use in treatment of mild traumatic brain injuries

Also Published As

Publication number Publication date
BR112016014000A2 (pt) 2017-08-08
PH12016501201A1 (en) 2016-08-15
WO2015095339A1 (fr) 2015-06-25
JP2017502031A (ja) 2017-01-19
EP3083656A1 (fr) 2016-10-26
AR098879A1 (es) 2016-06-22
MA39126A3 (fr) 2019-04-30
MA39126B1 (fr) 2020-03-31
CN105980396B (zh) 2019-03-22
MX2016008167A (es) 2017-04-27
TN2016000252A1 (en) 2017-10-06
CN105980396A (zh) 2016-09-28
AU2014364850A1 (en) 2016-07-07
US20150175650A1 (en) 2015-06-25
SG11201604982XA (en) 2016-07-28
TW201538519A (zh) 2015-10-16
CA2934466A1 (fr) 2015-06-25
UY35909A (es) 2015-07-31
EA201691074A1 (ru) 2017-02-28
IL246258A0 (en) 2016-08-02

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