SK127398A3 - Novel asymmetric synthesis of r-'alpha'-propyl-piperonyl amine and its analogs - Google Patents

Novel asymmetric synthesis of r-'alpha'-propyl-piperonyl amine and its analogs Download PDF

Info

Publication number
SK127398A3
SK127398A3 SK1273-98A SK127398A SK127398A3 SK 127398 A3 SK127398 A3 SK 127398A3 SK 127398 A SK127398 A SK 127398A SK 127398 A3 SK127398 A3 SK 127398A3
Authority
SK
Slovakia
Prior art keywords
compound
acid
hours
temperature
alcohol
Prior art date
Application number
SK1273-98A
Other languages
English (en)
Slovak (sk)
Inventor
Hui-Yin Li
Luigi Anzalone
Robert E Waltermire
Original Assignee
Du Pont Pharm Co
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 Pharm Co filed Critical Du Pont Pharm Co
Publication of SK127398A3 publication Critical patent/SK127398A3/sk

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)
SK1273-98A 1996-03-22 1997-03-17 Novel asymmetric synthesis of r-'alpha'-propyl-piperonyl amine and its analogs SK127398A3 (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 (1)

Publication Number Publication Date
SK127398A3 true SK127398A3 (en) 1999-04-13

Family

ID=21762727

Family Applications (1)

Application Number Title Priority Date Filing Date
SK1273-98A SK127398A3 (en) 1996-03-22 1997-03-17 Novel asymmetric synthesis of r-'alpha'-propyl-piperonyl amine and its analogs

Country Status (23)

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

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
ZA972342B (en) 1998-09-18
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

Similar Documents

Publication Publication Date Title
SK127398A3 (en) Novel asymmetric synthesis of r-'alpha'-propyl-piperonyl amine and its analogs
US5545745A (en) Enantioselective preparation of optically pure albuterol
JP2818958B2 (ja) 4―(4―アルコキシフェニル)―2―ブチルアミン誘導体およびその製造法
JP2009534385A (ja) キラル的に純粋なアミノアルコール中間体、それらの誘導体の製造、及びそれらの使用
US10087136B2 (en) Process for the preparation of Metaraminol
HUE033534T2 (en) Asymmetric synthesis of substituted pyrrolidine-2-carboxamide
JP5927126B2 (ja) 2−(シクロヘキシルメチル)−n−{2−[(2s)−1−メチルピロリジン−2−イル]エチル}−1,2,3,4−テトラヒドロイソキノリン−7−スルホンアミドの製造方法
JP2006028154A (ja) 光学活性化合物の製造方法
KR100939347B1 (ko) 광학적으로 순수한 (s)-3-히드록시 피롤리딘의 제조방법
HU227114B1 (en) (1r, 2s, 4r)-(-)-2-[n,n-(dimethylamino-ethoxy)]-2-phenyl-1,7,7-trimethyl-bicyclo[2.2.1]heptane of high purity and pharmaceutically acceptable acid addition salts thereof, process for preparation of them and medicaments containing the same
HU229188B1 (hu) Új eljárás N-[(S)-1-karboxibutil]-(S)-alanin-észterek elõállítására, és a perindopril szintézisnél történõ alkalmazása
WO2007080470A2 (en) A method for the purification of levetiracetam
JP3184758B2 (ja) 光学活性4−ヒドロキシ−2−ピロリドンの製造方法
WO2012022994A1 (en) Preparation process of vildagliptin
CA2996813A1 (en) Method for the production of praziquantel and precursors thereof
KR101239795B1 (ko) 피로글루타메이트 염 및 덱스트로세티리진 및레보세티리진을 합성하기 위한 중간체의 광학 분리에서의이들의 용도
WO2013090161A1 (en) Stereoselective synthesis of tapentadol and its salts
Wilken et al. Enantioselective Catalytic Borane Reduction of Prochiral Ketones: Synthesis and Application of New Rigid β-Amino Alcohols with a Cycloalkanol Subunit
US6593489B1 (en) Substituted cyclopentenes, their preparation and their use for chiral scaffolds
JP3159800B2 (ja) 光学異性体の分離法
HU205594B (en) Process for producing optical isomeres of cyclopropane-carboxylic acids5
JP3845884B2 (ja) N−〔1−(2,4−ジクロロフェニル)エチル〕−2−シアノ−3,3−ジメチルブタンアミドの製造法
JP2003171354A (ja) 光学活性アミン化合物又はその塩の製造方法
MXPA98007673A (es) Nueva sintesis asimetrica de r-alfa-propil-piperonil amina y sus analogos
JPH0813793B2 (ja) 酒石酸アミド誘導体