LV12259B - NEW R-ALFA-PROPILPIPERONYLAMINE AND ITS ANALOGUE SYNTHESIS - Google Patents

NEW R-ALFA-PROPILPIPERONYLAMINE AND ITS ANALOGUE SYNTHESIS Download PDF

Info

Publication number
LV12259B
LV12259B LVP-98-185A LV980185A LV12259B LV 12259 B LV12259 B LV 12259B LV 980185 A LV980185 A LV 980185A LV 12259 B LV12259 B LV 12259B
Authority
LV
Latvia
Prior art keywords
compound
acid
alcohol
formula
hydrogen
Prior art date
Application number
LVP-98-185A
Other languages
English (en)
Latvian (lv)
Other versions
LV12259A (lv
Inventor
Hui-Yin Li
Luigi Anzalone
Robert Eugene Waltermire
Original Assignee
Dupont Pharmaceuticals Company
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 Dupont Pharmaceuticals Company filed Critical Dupont Pharmaceuticals Company
Publication of LV12259A publication Critical patent/LV12259A/xx
Publication of LV12259B publication Critical patent/LV12259B/en

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
    • C07D317/44Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D317/46Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with one six-membered ring
    • C07D317/48Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring
    • C07D317/50Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to atoms of the carbocyclic ring
    • C07D317/58Radicals substituted by nitrogen atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

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)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Engineering & Computer Science (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Peptides Or Proteins (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
LVP-98-185A 1996-03-22 1998-09-21 NEW R-ALFA-PROPILPIPERONYLAMINE AND ITS ANALOGUE SYNTHESIS LV12259B (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US1395596P 1996-03-22 1996-03-22
PCT/US1997/003466 WO1997034887A1 (en) 1996-03-22 1997-03-17 NOVEL ASYMMETRIC SYNTHESIS OF R-α-PROPYL-PIPERONYL AMINE AND ITS ANALOGS

Publications (2)

Publication Number Publication Date
LV12259A LV12259A (lv) 1999-04-20
LV12259B true LV12259B (en) 1999-09-20

Family

ID=21762727

Family Applications (1)

Application Number Title Priority Date Filing Date
LVP-98-185A LV12259B (en) 1996-03-22 1998-09-21 NEW R-ALFA-PROPILPIPERONYLAMINE AND ITS ANALOGUE SYNTHESIS

Country Status (23)

Country Link
US (1) US5932749A (no)
EP (1) EP0888329A1 (no)
JP (1) JP2000506891A (no)
KR (1) KR20000064735A (no)
CN (1) CN1218463A (no)
AR (1) AR006521A1 (no)
AU (1) AU719633B2 (no)
BR (1) BR9708233A (no)
CA (1) CA2249401A1 (no)
CZ (1) CZ295098A3 (no)
EA (1) EA001207B1 (no)
EE (1) EE9800299A (no)
HR (1) HRP970165A2 (no)
IL (1) IL126223A0 (no)
LT (1) LT4540B (no)
LV (1) LV12259B (no)
NO (1) NO984344D0 (no)
NZ (1) NZ331875A (no)
PL (1) PL329070A1 (no)
SI (1) SI9720023A (no)
SK (1) SK127398A3 (no)
WO (1) WO1997034887A1 (no)
ZA (1) ZA972342B (no)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000012474A1 (en) 1998-08-31 2000-03-09 Du Pont Pharmaceuticals Company An efficient process for the preparation of a human leukocyte elastase inhibitor
PL372705A1 (en) * 2001-09-12 2005-07-25 Anormed Inc. Synthesis of enantiomerically pure amino-substituted fused bicyclic rings
EA022785B8 (ru) * 2008-12-15 2016-06-30 Тайджен Байотекнолоджи Ко., Лтд. Стереоселективный синтез производных пиперидина
AR090100A1 (es) 2012-02-21 2014-10-22 Celgene Corp Procesos para la preparacion de la (s)-1-(3-etoxi-4-metoxifenil)-2-metanosulfoniletilamina
US9126906B2 (en) 2012-02-21 2015-09-08 Celgene Corporation Asymmetric synthetic processes for the preparation of aminosulfone compounds
US10953003B2 (en) 2015-12-14 2021-03-23 X4 Pharmaceuticals, Inc. Methods for treating cancer
CA3008279A1 (en) 2015-12-14 2017-06-22 X4 Pharmaceuticals, Inc. Methods for treating cancer
SI3393468T1 (sl) 2015-12-22 2023-01-31 X4 Pharmaceuticals, Inc. Postopki za zdravljenje bolezni imunske pomanjkljivosti
US11337969B2 (en) 2016-04-08 2022-05-24 X4 Pharmaceuticals, Inc. Methods for treating cancer
EP3808748A1 (en) 2016-06-21 2021-04-21 X4 Pharmaceuticals, Inc. Substituted piperidines as cxcr4-inhibitors
US11332470B2 (en) 2016-06-21 2022-05-17 X4 Pharmaceuticals, Inc. CXCR4 inhibitors and uses thereof
JP7084624B2 (ja) 2016-06-21 2022-06-15 エックス4 ファーマシューティカルズ, インコーポレイテッド Cxcr4阻害剤およびその使用
US10548889B1 (en) 2018-08-31 2020-02-04 X4 Pharmaceuticals, Inc. Compositions of CXCR4 inhibitors and methods of preparation and use
WO2023034510A1 (en) 2021-09-01 2023-03-09 ATAI Life Sciences AG Synthesis of mdma or its optically active ( r)- or ( s)-mdma isomers
EP4401725A1 (en) * 2021-09-17 2024-07-24 atai Life Sciences AG Preparation of optically active enantiomers of piperonyl amines by resolution of the diastereomeric salts
US11845736B2 (en) 2021-10-01 2023-12-19 Empathbio, Inc. Prodrugs of MDMA, MDA, and derivatives thereof
US11912680B2 (en) 2021-12-28 2024-02-27 Empathbio, Inc. Nitric oxide releasing prodrugs of MDA and MDMA

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3819438A1 (de) * 1987-06-30 1989-01-19 Basf Ag Verfahren zur herstellung von optisch aktiven 1-arylethylaminen
IL99658A0 (en) * 1990-10-15 1992-08-18 Merck & Co Inc Substituted azetidinones and pharmaceutical compositions containing them
US5149838A (en) * 1991-09-20 1992-09-22 Merck & Co., Inc. Intermediates for substituted azetidinones useful as anti-inflammatory and antidegenerative agents

Also Published As

Publication number Publication date
KR20000064735A (ko) 2000-11-06
EE9800299A (et) 1999-06-15
HRP970165A2 (en) 1998-04-30
BR9708233A (pt) 2000-01-04
CN1218463A (zh) 1999-06-02
EA001207B1 (ru) 2000-12-25
NO984344L (no) 1998-09-18
ZA972342B (en) 1998-09-18
AU719633B2 (en) 2000-05-11
CA2249401A1 (en) 1997-09-25
LT98132A (en) 1999-03-25
PL329070A1 (en) 1999-03-15
AR006521A1 (es) 1999-09-08
SI9720023A (sl) 1999-04-30
US5932749A (en) 1999-08-03
JP2000506891A (ja) 2000-06-06
WO1997034887A1 (en) 1997-09-25
CZ295098A3 (cs) 1999-03-17
EA199800844A1 (ru) 1999-02-25
LT4540B (lt) 1999-08-25
EP0888329A1 (en) 1999-01-07
NZ331875A (en) 2000-01-28
NO984344D0 (no) 1998-09-18
AU2196897A (en) 1997-10-10
SK127398A3 (en) 1999-04-13
IL126223A0 (en) 1999-05-09
LV12259A (lv) 1999-04-20

Similar Documents

Publication Publication Date Title
LV12259B (en) NEW R-ALFA-PROPILPIPERONYLAMINE AND ITS ANALOGUE SYNTHESIS
JP2007525532A (ja) N−アルキル−n−メチル−3−ヒドロキシ−3−(2−チエニル)−プロピルアミンの製造方法
KR20070057703A (ko) 거울상 이성체적으로 순수한 아토목세틴 및 토목세틴만델레이트
JP5254836B2 (ja) ベナゼプリル及びその類似体の生産に有用な中間体の速度論的分離
MX2007014781A (es) Proceso para la resolucion dinamica de acido (r) o (s)-mandelico (substituido).
JP4718452B2 (ja) 光学活性遷移金属−ジアミン錯体及びこれを用いた光学活性アルコール類の製造方法
KR100794091B1 (ko) 2-에톡시-3-(4-히드록시페닐)프로판산 및 그의 유도체의 (s)-거울상이성질체의 제조 방법
CA2431400C (en) Process for preparing isomers of salbutamol
KR100712003B1 (ko) 펜세린 및 그 유사체의 제조방법
CH648314A5 (fr) Procede de preparation de trans-5-aryl-2,3,4,4a,5,9b-hexahydro-1h-pyrido(4,3-b)-indoles substitues en position 2 et composes permettant de les obtenir.
JPH0469145B2 (no)
CA2276074A1 (en) Efficient synthesis of a chiral mediator
JPH10218847A (ja) タートラニル酸の製造法
CN114621126B (zh) 一种改进的依折麦布的制备方法
MXPA98007673A (en) New asymmetric synthesis of r-alpha-propil-piperonil amine and its analo
JP2825608B2 (ja) 光学活性トレオ―3―アミノ―2―ヒドロキシペンタン酸及びその製造法
JP2002371060A (ja) 光学活性アミノピペリジン誘導体の製造方法
JP3010756B2 (ja) 光学活性アルコールの製造方法
CN111333544A (zh) 一种用于合成尼拉帕尼的中间体及其制备方法
JP2013129642A (ja) 光学活性3,4−ビス(アルキルオキシカルボニル)−1,6−ヘキサン二酸誘導体の製造法
CN115784907A (zh) 一种dl-去氧肾上腺素的制备方法
JPWO2002044136A1 (ja) N保護−β−アミノアルコールの製造法およびN保護−β−アミノエポキシドの製造法
WO2005009972A2 (en) Process for preparation of benazepril
JPH041744B2 (no)
JPS5984863A (ja) 4―メチリデン―4,5,6,7―テトラヒドロインドール誘導体