PL125785B1 - Process for preparing novel octahydro-2h-pyrrole /3,4-g/-quinolines - Google Patents

Process for preparing novel octahydro-2h-pyrrole /3,4-g/-quinolines Download PDF

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Publication number
PL125785B1
PL125785B1 PL1979216721A PL21672179A PL125785B1 PL 125785 B1 PL125785 B1 PL 125785B1 PL 1979216721 A PL1979216721 A PL 1979216721A PL 21672179 A PL21672179 A PL 21672179A PL 125785 B1 PL125785 B1 PL 125785B1
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PL
Poland
Prior art keywords
group
quinolines
pyrrole
preparing novel
acid
Prior art date
Application number
PL1979216721A
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English (en)
Other versions
PL216721A1 (pl
Original Assignee
Lilly Co Eli
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
Priority claimed from US06/031,642 external-priority patent/US4235909A/en
Application filed by Lilly Co Eli filed Critical Lilly Co Eli
Publication of PL216721A1 publication Critical patent/PL216721A1/xx
Publication of PL125785B1 publication Critical patent/PL125785B1/pl

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom 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
    • C07D215/20Oxygen atoms
    • C07D215/22Oxygen atoms attached in position 2 or 4
    • C07D215/227Oxygen atoms attached in position 2 or 4 only one oxygen atom which is attached in position 2
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom 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
    • C07D215/20Oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom 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
    • C07D215/48Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
    • C07D215/54Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 3
    • 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

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  • 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)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Description

Przedmiotem wynalazku jest sposób wytwarza¬ nia nowych olklUhyKlro^2H^i^o^O'I3»4Hg]thirwlin o Ogólnym wzorze 1, w którym R oznacza grupe alkilowa o 1—3 atomach wegla lufo grupe allilowa onaz ich farmakologicznie rozpuszczalnych soli ad¬ dycyjnych z kwasami Sposób wedlug wynalazku polega na tym, ze zwialzek o ogólnym wzorze lc, w którym R1 ozna¬ cza grupe alkilokaribonylowa o 1M3 atomach we¬ gla w czesci alkilowej, a R ma wyzerj podane znaczenie, poddaje sie reakcji z zasada i ewen¬ tualnie wyftwarza sie farmakologicznie dopuszczal¬ ne sole postepujac w znany sposób. Zwiazki o wzorze lc sa nowe* fcwiiaizki o wzorze 1 maja w pierscieniu wspól¬ ne wiazanie 4a, 8a o konfiguracji' trans, a zwiaz¬ ki te otrzymuje sie jako mieszanine raceimiczna.Budowe dwóch sitereoizomerów skladajacych sie na raieetmat przedstawiaja wzory la i l.b.Bez wzgledu na strukture przypisana aktualnie danemu izomerowi luib mieszaninie racemicznej sposobem wedlug wynalazku otrzymuje siie zwiaz¬ ki o wzorze 11, wykazujace dzialanie agoniisty wzgledem dopaminy, czy to w czysltej posftaci jako pojedynczy diastereoizomer czy zmieszany z jed- nyim luib kilkoma mniej aktywnymi lub nawet nieaktywnymi diaistereoizdrnierami., Okreslenie grupa alkilowa o 1—& atomach we¬ gla oznacza grupe metylowa, etylowa, n-propylo- wa i izopropylowa. 15 20 25 30 Do dopuszczalnych w farmacji soli addycyjnych z kwasami naleza Sole z kwasami nieorganiczny¬ mi takimi jak khvas' chlorowodorowy, azotowy, fosforowy, siarkowy., bromdwodorowy, jodowodo- nowy, azotawy, fosforowy i tym poddbne, jak róiw- niez sole z nieltofcsyoznymi kwasami organicznymi, takimi jak jedno- i dwukarlboklsylowe kwasy ali¬ fatyczne, fenylopodstawione kwasy alkanokoTiba- ksylowe, kwasy hydroksyalkanokarlboksylowe i hy- droksyalkanodwukariboksylloiwe, kwasy aromatycz¬ ne, alitfaitycznie i aromatyczne kwasy sulfonowe.Po takich dopuszczalnych w farmacji soli nale*- za zatem: siarczany, pirosiarczany, wodorosiarcza¬ ny, siarczyny, wodórosiarczyny, azotany, fostfofany, j^dnlowodorofosforany, dwuwodorofosforany, meta- fosforany, pirofosiforany, chlorki, bromki, jodki; fluorki, octany, propioniany, kapryniany, kapryla- ny, akrylany, mrówczany, izomaslany, kaproniany, sole kwasu enanlowego, propiolany, szczawiany, malloniany, bursztyniany, suiberyniany, sebacynia- ny, fumarany, maleiniany, migdalany, sole kwasu eH;ynoJl,2Jdwukarlboklsylowe^o, bu|tynoJl',44dwukar- iboks-ylowiego, benzoesany, chlorolbenzoesany, mety- loibenzoesahy, dlwunitrdbenizoesany, hydroksybenzo- esany, metoksyfbenzoesany, iftalany, tereftalany, benzenosulfoniany, toluenosulfoniany, chlorobenze- nosulfoniany, ksylenosullfoniany, fenylooctany, fe- nylopropionrany, fenyloniaslany,, cytryniany, mle¬ czany, hiydrofcsymleczany, glikondany, jalbftczany, winiany, metaniosultoiiany, propanosulfoniany, na- 125 7853 125 785 4 ftalenomMsaiifaniany, naifteleno^-sulifoniany i tym podoibne sole* (Przykladami zwiadów dbjejtych wzorem 1 sa: chlorowodorek lTans^DLJ5-Tneltylo-l4i,4aAl&,r7A8ia^- ^oflcta(hydr<^H^iTyId[l3'l4^]!cMnol!iny, irans-DL-5- ni^iTopylb^%j5J8^^ ,[3j4Hg]chinolina, ^aziS^Dt^Sr^y^o^^Bi^/lfij^J^ ¦*oktalhydio^2IH-Tiiirolo[^ i toans-D(Lr^- -allilO^aA^iB^^ - chinolina.Zwiazki o wzorze 1 otrzymuje sie sposobem przedstawionym na schemacie. Na tym schemacie dla wygody zaznaczono tylko jeden stereoizomer lecz nalezy jednak pamietac, ze kazlda dekahydlro- chinolina i kaizda okliaihydropirolofS^^lchdiiollina wyisitepufie jako inoeszanina racemiczna. Ponadto R oznacza gru|pe inna niz aten wodoru.(Na schemacie gruJpa* Z-OO oznacza acylowa gru¬ pe zabezpieczajaca, z której Z oznacza grupe alki¬ lowa o !«—£ atomach wejgja, grupe aUkenylowa o 2—3 atomach wegla, grupe cykloalkilowa o 5^6 atomach wegla, grupe fenylowa lub podstawiona grupe fenylowa, przy czym podstawnikiem rrioze byc grupa metyilotwa, ineloksylowa* altom chloru itlpy w dowolhym polazeniu pierscienia fenyllowe- go. Na przyklad ZOO moze oznaczac grupe ace- tylowa, propionylowa, butyrylowa, propdolilowa, akrylilowa, benzoilowa, rHtoluilowa, chlorofjenzo- ilowa luib m-metoksylbenzoilowa.Acetale dimetyloformamidu sltosowane przy wytwarzaniu zwiajzków o wzorze 8 wediug sche¬ matu okresla, ogólny wzór (CJH*^N<3Hi/10IZ,7i, w któryni Z" oznacza' grutpe alkilowa o 1—3 ato¬ mach wejgla, grupe cykloalkilowa o S-^6 atomach wegla, grupe aikenylowa o &—4 atomalch wegla, grupe adkinylowa o $-^4 atomach wegla itp. Ko¬ rzystne jest stosowanie dostepnych w handlu ace¬ tali dwumetylotCormamldu, takich jak acetal dwu- metylowy, dwuatyilowy, dwuizopropylowy, dwuDbu- tytowy, dwucyfcllofoeksylowy, dwupro|pylowy lub dwuneopenitylowy, Zfeodmie ze slehemafcem, 4-acyMcsycylohJeksanol (zwiazek o wzorze 2) otrzymany sposobem opisa¬ nym przez ERH Jonasla i F. Sondneimera J. Chem.Soc., 01$ {UW©), poddaje sie reakcji z pirolijdyna w obecnosci katalizatora kwasowego otrzymujac enamdne pirolMyny. Taka enamtine poddaje sfle z któtei reakcji z aterylamldem ottrzymujajc mieszani¬ ne DL^^eylokB7^^,6/?,^^ noHny i DL-6-acyloksy-3,4,4a^,6,7-hekisahydro- -aUHA-chinoliny o wzorze 3, przy czym linie prze¬ rywane wskazuja alternatywne polozenia podwój¬ nego wiazania.Nastepnie kjwasowy atom azotu (kwasowy gdyz znajduje sfle w polozeniu altfia w stosunku do grupy karbonylowej) poddaje sie alkilowaniu przy uzy¬ ciu halogenku aifcrlu EX, w którym R ma poda¬ ne powyzej znaczenie, a X oznacza atom chlorow¬ ca talki jak aibom chloru, bromu lufo jodu, w obec¬ nosci wodorku sodowego z utworzeniem miesza¬ niny DLJl 4A^73^h€k5ahjHdro^lH^chitti PL PL PL PL PL PL PL

Claims (1)

1.
PL1979216721A 1979-01-22 1979-06-29 Process for preparing novel octahydro-2h-pyrrole /3,4-g/-quinolines PL125785B1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US506279A 1979-01-22 1979-01-22
US06/031,642 US4235909A (en) 1979-04-19 1979-04-19 Octahydro-2H-pyrrolo[3,4-g]quinolines

Publications (2)

Publication Number Publication Date
PL216721A1 PL216721A1 (pl) 1980-06-16
PL125785B1 true PL125785B1 (en) 1983-06-30

Family

ID=26673871

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Application Number Title Priority Date Filing Date
PL1979216721A PL125785B1 (en) 1979-01-22 1979-06-29 Process for preparing novel octahydro-2h-pyrrole /3,4-g/-quinolines

Country Status (25)

Country Link
EP (1) EP0013788B1 (pl)
JP (1) JPS55100385A (pl)
AR (1) AR225012A1 (pl)
AT (1) AT365189B (pl)
AU (1) AU528035B2 (pl)
BE (1) BE877328A (pl)
CA (1) CA1131227A (pl)
CH (2) CH641801A5 (pl)
DD (1) DD144668A5 (pl)
DE (1) DE2965277D1 (pl)
DK (1) DK268979A (pl)
ES (1) ES482084A1 (pl)
FI (1) FI65248C (pl)
FR (2) FR2446833A1 (pl)
GB (1) GB2040917B (pl)
IE (1) IE48295B1 (pl)
IL (1) IL57665A (pl)
LU (1) LU81440A1 (pl)
NZ (1) NZ190834A (pl)
PH (2) PH15118A (pl)
PL (1) PL125785B1 (pl)
PT (1) PT69828A (pl)
RO (1) RO77442A (pl)
SU (1) SU1113006A3 (pl)
ZA (1) ZA793244B (pl)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IL65269A0 (en) * 1981-03-24 1982-05-31 Lilly Co Eli 6-substituted hexahydroindazolo or hexahydroisoindolo isoquinolines
DE3373468D1 (de) * 1983-06-03 1987-10-15 Lilly Co Eli Trans-dl-1-alkyl-6-alkoxyoctahydroquinolines
IL73001A0 (en) * 1983-09-26 1984-12-31 Lilly Co Eli Improvements in and relating to 6-oxodecahydroquinolines
US4595754A (en) * 1985-03-04 1986-06-17 Eli Lilly And Company Process for preparing cis N-alkylperhydroquinolines
TW200904817A (en) * 2007-06-19 2009-02-01 Astrazeneca Ab Compounds and uses thereof
TWI537274B (zh) * 2011-03-14 2016-06-11 橘生藥品工業股份有限公司 新穎之八氫噻吩并喹啉衍生物、含有其之醫藥組成物及該等之用途

Also Published As

Publication number Publication date
ES482084A1 (es) 1980-08-01
CA1131227A (en) 1982-09-07
FR2446833B1 (pl) 1982-03-05
FI792047A7 (fi) 1980-07-23
GB2040917B (en) 1983-01-06
AU4844479A (en) 1980-07-31
ATA452579A (de) 1981-05-15
EP0013788A1 (en) 1980-08-06
CH641801A5 (fr) 1984-03-15
FR2446835A1 (fr) 1980-08-14
FR2446835B1 (pl) 1982-04-23
JPS6233233B2 (pl) 1987-07-20
JPS55100385A (en) 1980-07-31
PL216721A1 (pl) 1980-06-16
LU81440A1 (fr) 1979-09-12
CH643258A5 (fr) 1984-05-30
BE877328A (fr) 1979-12-28
AU528035B2 (en) 1983-04-14
IE48295B1 (en) 1984-11-28
DD144668A5 (de) 1980-10-29
PH15118A (en) 1982-08-10
DE2965277D1 (en) 1983-06-01
NZ190834A (en) 1984-07-06
EP0013788B1 (en) 1983-04-27
SU1113006A3 (ru) 1984-09-07
FI65248B (fi) 1983-12-30
FR2446833A1 (fr) 1980-08-14
PH16181A (en) 1983-07-25
ZA793244B (en) 1981-02-25
RO77442A (ro) 1982-10-26
PT69828A (en) 1979-07-01
FI65248C (fi) 1984-04-10
AT365189B (de) 1981-12-28
DK268979A (da) 1980-07-23
IL57665A0 (en) 1979-10-31
GB2040917A (en) 1980-09-03
IL57665A (en) 1982-11-30
IE791210L (en) 1980-10-19
AR225012A1 (es) 1982-02-15

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