YU48311B - Postupak za dobijanje racemskih ili optički aktivnih perhidro-1h-pirido /1,2-a/pirazina - Google Patents

Postupak za dobijanje racemskih ili optički aktivnih perhidro-1h-pirido /1,2-a/pirazina

Info

Publication number
YU48311B
YU48311B YU19892A YU19892A YU48311B YU 48311 B YU48311 B YU 48311B YU 19892 A YU19892 A YU 19892A YU 19892 A YU19892 A YU 19892A YU 48311 B YU48311 B YU 48311B
Authority
YU
Yugoslavia
Prior art keywords
pirido
pyrazine
procedure
optically active
alkyl
Prior art date
Application number
YU19892A
Other languages
English (en)
Other versions
YU19892A (sh
Inventor
G.M. Bright
K.A. Desai
T.F. Seeger
Original Assignee
Pfizer 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 Pfizer Inc. filed Critical Pfizer Inc.
Publication of YU19892A publication Critical patent/YU19892A/sh
Publication of YU48311B publication Critical patent/YU48311B/sh

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D211/60Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/18Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D211/60Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D211/62Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals attached in position 4
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • 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
    • Y02P20/582Recycling of unreacted starting or intermediate materials

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Psychiatry (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Abstract

POSTUPAK ZA DOBIJANJE RACEMSKIH ILI OPTICKI AKTIVNIH PERHIDRO-1H-PIRIDO /1,2-A/PIRAZINA formule u kojoj: L i X kada su uzeti odvojeno, X je H ili Cl alkil sa C2 i L je R(CH2)mCO, ili L i X uzeti zajedno predstavljaju R je C1 do C8 alkil, C3 do C7 cikloalkil, fenil, naftil, furil, benzofuranil, tienil, benzotienil, pirolil, indolil, izoindolil, norbornilmetil, ili jedna od pomenutih grupa supstituisana u aromaticnom ili heteroaromaticnom prstenu sa F, C1, C1 do C2 alkil ili C1 do C2 alkoksi grupom; R1, R2 i R3 su svaki nezavisno H ili metil; R4 je fenil ili fenil supstituisan sa F, C1, C1 do C2 alkil ili C1 do C" alkoksi grupom; X1 je CH ili N; Y je O ili S; Y1 je CH2, S, O ili NH; Y2 i Y3 su uzeti odvojeno i predstavljaju nezavisno H ili metil ili Y2 i Y3 kada su uzeti zajedno predstavljaju (CH2)q; Z je H ili C1; m je O, 1, 2 ili 3; n je 1, 2, 3 ili 4; p je 1 ili 2; q je 2, 3, 4 ili 5; r je O ili 1; s je O ili 1; i predstavlja vezu ili nije veza, naznacen time, sto obuhvata (a) kada su L i X uzeti odvojeno, acilovanje jedinjenja formule u kojoj X, Y i n su kao sto je gore definisano, reakciju sa aktiviranim oblikom jedinjenja formule R (CH2)mCOOH, gde R i m su kao sto je gore definisano; (b) kada L i X su uzeti zajedno, reakciju jedinjenja formule u kojoj Y i n su kao sto je gore definisano, a D je nukleofilna grupa koja se moze zameniti, u reakciono inertnom rastvaracu, sa (i) kada L i X zajedno obrazuju imid ili ciklicni sulfonamid, njegov anjonski derivat, ili (ii) kada L i X zajedno obrazuju prost piperidinski derivat, njegov oblik slobodnog amina; ili (c) reakciju, pod uslovima nukleofilnog premestanja, jedinjenja formule u kojoj L, X i n su kao sto je gore definisano, sa jedinjenjem formule u kojoj Y i Z su kao sto je gore definisano. Prijava sadrzi jos 18 zavisnih zahteva.
YU19892A 1991-02-27 1992-02-26 Postupak za dobijanje racemskih ili optički aktivnih perhidro-1h-pirido /1,2-a/pirazina YU48311B (sh)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US07/661,791 US5157034A (en) 1991-02-27 1991-02-27 Neuroleptic perhydro-1H-pyrido[1,2-a]pyrazines

Publications (2)

Publication Number Publication Date
YU19892A YU19892A (sh) 1994-11-15
YU48311B true YU48311B (sh) 1998-05-15

Family

ID=24655130

Family Applications (1)

Application Number Title Priority Date Filing Date
YU19892A YU48311B (sh) 1991-02-27 1992-02-26 Postupak za dobijanje racemskih ili optički aktivnih perhidro-1h-pirido /1,2-a/pirazina

Country Status (24)

Country Link
US (1) US5157034A (sh)
EP (1) EP0573467B1 (sh)
JP (1) JP2546770B2 (sh)
KR (1) KR0163413B1 (sh)
AT (1) ATE123284T1 (sh)
AU (1) AU652422B2 (sh)
CA (2) CA2101518C (sh)
DE (2) DE9190206U1 (sh)
DK (1) DK0573467T3 (sh)
ES (1) ES2073914T3 (sh)
FI (3) FI105030B (sh)
HU (1) HU216637B (sh)
IE (1) IE67190B1 (sh)
IL (2) IL101021A (sh)
MX (1) MX9200803A (sh)
MY (1) MY108185A (sh)
NO (1) NO300847B1 (sh)
NZ (1) NZ241739A (sh)
PT (1) PT100160B (sh)
RU (1) RU2090565C1 (sh)
TW (1) TW207540B (sh)
WO (1) WO1992015580A1 (sh)
YU (1) YU48311B (sh)
ZA (1) ZA921405B (sh)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2101252C (en) * 1991-02-27 1998-02-17 Frank J. Urban Process for preparing trans-piperidine-2,5- dicarboxylates
JP2753146B2 (ja) * 1992-06-16 1998-05-18 ファイザー・インコーポレーテッド ビス−アザー二環式抗不安薬の製法および中間体
JP3287574B2 (ja) * 1994-09-30 2002-06-04 ファイザー・インク 2,7−置換オクタヒドロ−1h−ピリド[1,2−a]ピラジン誘導体
US6231833B1 (en) 1999-08-05 2001-05-15 Pfizer Inc 2,7-substituted octahydro-1H-pyrido[1,2-A]pyrazine derivatives as ligands for serotonin receptors
WO1996010570A1 (en) * 1994-09-30 1996-04-11 Pfizer Inc. NEUROLEPTIC 2,7-DISUBSTITUTED PERHYDRO-1H-PYRIDO[1,2-a]PYRAZINES
PA8469101A1 (es) * 1998-04-09 2000-09-29 Pfizer Prod Inc Ligandos azabiciclicos de receptores 5ht1
UA62015C2 (en) * 1998-12-28 2003-12-15 Pfizer Prod Inc Benzoizoxazol derivatives, a pharmaceutical composition (variants) based thereon (variants) and a method for treatment (variants)
PL378749A1 (pl) * 2003-03-12 2006-05-15 Pfizer Products Inc. Azabicykliczne pochodne pirydyloksymetylowe i benzoizoksazolowe
PL1622569T3 (pl) 2003-04-24 2016-06-30 Incyte Holdings Corp Pochodne aza spiro alkanów jako inhibitory metaloproteaz
US7910108B2 (en) * 2006-06-05 2011-03-22 Incyte Corporation Sheddase inhibitors combined with CD30-binding immunotherapeutics for the treatment of CD30 positive diseases
EP2919788A4 (en) 2012-11-14 2016-05-25 Univ Johns Hopkins METHODS AND COMPOSITIONS FOR THE TREATMENT OF SCHIZOPHRENIA

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4681938A (en) * 1984-08-27 1987-07-21 Ciba-Geigy Corporation Novel polycyclic hydrazones of rifamycins, their manufacture, and their pharmaceutical compositions for treating tuberculosis
US4831031A (en) * 1988-01-22 1989-05-16 Pfizer Inc. Aryl piperazinyl-(C2 or C4) alkylene heterocyclic compounds having neuroleptic activity
US4957916A (en) * 1988-08-05 1990-09-18 Janssen Pharmaceutica N.V. Antipsychotic 3-piperazinylbenzazole derivatives
MX19222A (es) * 1989-01-23 1993-12-01 Pfizer Agentes ansioliticos bis-aza-biciclicos

Also Published As

Publication number Publication date
HU9302427D0 (en) 1993-11-29
FI933753A0 (fi) 1993-08-26
CA2101518C (en) 1997-11-25
US5157034A (en) 1992-10-20
FI933753A (fi) 1993-08-26
ZA921405B (en) 1993-08-26
ES2073914T3 (es) 1995-08-16
FI20000354A (fi) 2000-02-17
IL101021A (en) 1996-03-31
JPH06500120A (ja) 1994-01-06
ATE123284T1 (de) 1995-06-15
MY108185A (en) 1996-08-30
FI114214B (fi) 2004-09-15
FI20030361A (fi) 2003-03-11
HU216637B (hu) 1999-07-28
IE67190B1 (en) 1996-03-06
JP2546770B2 (ja) 1996-10-23
MX9200803A (es) 1992-08-31
PT100160A (pt) 1993-05-31
YU19892A (sh) 1994-11-15
CA2163274C (en) 1999-02-09
RU2090565C1 (ru) 1997-09-20
DE69110135T2 (de) 1995-10-19
HUT66965A (en) 1995-01-30
DE9190206U1 (de) 1993-10-14
DK0573467T3 (da) 1995-10-09
NZ241739A (en) 1994-07-26
NO300847B1 (no) 1997-08-04
IL112325A0 (en) 1995-03-30
KR930703315A (ko) 1993-11-29
WO1992015580A1 (en) 1992-09-17
EP0573467A1 (en) 1993-12-15
CA2101518A1 (en) 1992-08-28
FI105030B (fi) 2000-05-31
AU652422B2 (en) 1994-08-25
EP0573467B1 (en) 1995-05-31
FI112865B (fi) 2004-01-30
IE920601A1 (en) 1992-09-09
KR0163413B1 (ko) 1998-12-01
NO933049L (no) 1993-08-26
PT100160B (pt) 1999-09-30
NO933049D0 (no) 1993-08-26
DE69110135D1 (de) 1995-07-06
TW207540B (sh) 1993-06-11
CA2163274A1 (en) 1992-08-28
AU1259992A (en) 1992-10-06
IL112325A (en) 1997-08-14

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