ZA972342B - Asymmetric synthesis or R-alpha-propyl-piperonyl amine and its analogs - Google Patents

Asymmetric synthesis or R-alpha-propyl-piperonyl amine and its analogs

Info

Publication number
ZA972342B
ZA972342B ZA972342A ZA972342A ZA972342B ZA 972342 B ZA972342 B ZA 972342B ZA 972342 A ZA972342 A ZA 972342A ZA 972342 A ZA972342 A ZA 972342A ZA 972342 B ZA972342 B ZA 972342B
Authority
ZA
South Africa
Prior art keywords
analogs
propyl
alpha
asymmetric synthesis
piperonyl amine
Prior art date
Application number
ZA972342A
Other languages
English (en)
Inventor
Hui-Yin Li
Luigi Anzalone
Robert Eugene Waltermire
Original Assignee
Du Pont Merck Pharma
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 Du Pont Merck Pharma filed Critical Du Pont Merck Pharma
Publication of ZA972342B publication Critical patent/ZA972342B/xx

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)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Peptides Or Proteins (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
ZA972342A 1996-03-22 1997-03-18 Asymmetric synthesis or R-alpha-propyl-piperonyl amine and its analogs ZA972342B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US1395596P 1996-03-22 1996-03-22

Publications (1)

Publication Number Publication Date
ZA972342B true ZA972342B (en) 1998-09-18

Family

ID=21762727

Family Applications (1)

Application Number Title Priority Date Filing Date
ZA972342A ZA972342B (en) 1996-03-22 1997-03-18 Asymmetric synthesis or R-alpha-propyl-piperonyl amine and its analogs

Country Status (23)

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

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU5587299A (en) 1998-08-31 2000-03-21 Du Pont Pharmaceuticals Company An efficient process for the preparation of a human leukocyte elastase inhibitor
CN101353324A (zh) * 2001-09-12 2009-01-28 阿诺麦德股份有限公司 对映体纯的氨基取代稠合双环的合成
TWI386395B (zh) * 2008-12-15 2013-02-21 Taigen Biotechnology Co Ltd 哌啶衍生物的立體有擇合成
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
CN109069426B (zh) 2015-12-14 2021-10-29 X4 制药有限公司 治疗癌症的方法
WO2017106332A1 (en) 2015-12-14 2017-06-22 X4 Pharmaceuticals, Inc. Methods for treating cancer
US10610527B2 (en) 2015-12-22 2020-04-07 X4 Pharmaceuticals, Inc. Methods for treating immunodeficiency disease
JP2019510785A (ja) 2016-04-08 2019-04-18 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 癌を処置する方法
CA3027500A1 (en) 2016-06-21 2017-12-28 X4 Pharmaceuticals, Inc. Cxcr4 inhibitors and uses thereof
CA3027495A1 (en) 2016-06-21 2017-12-28 X4 Pharmaceuticals, Inc. Cxcr4 inhibitors and uses thereof
JP7054529B2 (ja) 2016-06-21 2022-04-14 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
WO2023044027A1 (en) * 2021-09-17 2023-03-23 ATAI Life Sciences AG Preparation of optically active enantiomers of piperonyl amines by resolution of the diastereomeric salts
WO2023056102A1 (en) 2021-10-01 2023-04-06 ATAI Life Sciences AG Novel 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
CN1218463A (zh) 1999-06-02
EP0888329A1 (en) 1999-01-07
EA199800844A1 (ru) 1999-02-25
IL126223A0 (en) 1999-05-09
WO1997034887A1 (en) 1997-09-25
LT98132A (en) 1999-03-25
PL329070A1 (en) 1999-03-15
JP2000506891A (ja) 2000-06-06
EA001207B1 (ru) 2000-12-25
AU2196897A (en) 1997-10-10
NZ331875A (en) 2000-01-28
NO984344L (no) 1998-09-18
HRP970165A2 (en) 1998-04-30
US5932749A (en) 1999-08-03
AU719633B2 (en) 2000-05-11
CA2249401A1 (en) 1997-09-25
AR006521A1 (es) 1999-09-08
BR9708233A (pt) 2000-01-04
LV12259B (en) 1999-09-20
SI9720023A (sl) 1999-04-30
LT4540B (lt) 1999-08-25
LV12259A (lv) 1999-04-20
KR20000064735A (ko) 2000-11-06
EE9800299A (et) 1999-06-15
CZ295098A3 (cs) 1999-03-17
NO984344D0 (no) 1998-09-18
SK127398A3 (en) 1999-04-13

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