PL130918B1 - Process for preparing pyrbuterol - Google Patents

Process for preparing pyrbuterol Download PDF

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Publication number
PL130918B1
PL130918B1 PL1982239428A PL23942882A PL130918B1 PL 130918 B1 PL130918 B1 PL 130918B1 PL 1982239428 A PL1982239428 A PL 1982239428A PL 23942882 A PL23942882 A PL 23942882A PL 130918 B1 PL130918 B1 PL 130918B1
Authority
PL
Poland
Prior art keywords
formula
pirbuterol
scheme
weak base
formaldehyde
Prior art date
Application number
PL1982239428A
Other languages
English (en)
Other versions
PL239428A1 (en
Original Assignee
Pfizer
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.)
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Publication date
Application filed by Pfizer filed Critical Pfizer
Publication of PL239428A1 publication Critical patent/PL239428A1/xx
Publication of PL130918B1 publication Critical patent/PL130918B1/pl

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/89Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members with hetero atoms directly attached to the ring nitrogen atom
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/08Bronchodilators
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/04Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen 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
    • C07D213/62Oxygen or sulfur atoms
    • C07D213/63One oxygen atom
    • C07D213/65One oxygen atom attached in position 3 or 5
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/04Ortho-condensed systems

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Veterinary Medicine (AREA)
  • Cardiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Hospice & Palliative Care (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Pulmonology (AREA)
  • Pyridine Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Steroid Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Catalysts (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Description

Przedmiotem wynalazku jest sposób wytwarzania pirbuterolu o wzorze 1.Zwiazek o wzorze 1 jest znanym srodkiem powodujacym rozszerzanie oskrzeli.Pirbuterol, jak równiez jego wlasciwosci i sposób wytwarzania, sa znane z opisów patentowych St. Zj. Am. nr nr 3700681, 3763173, 3772314 i 3786160. Sposób ten polega na reakcjach, których przebieg przedstawia schemat 1.Inny sposób wytwarzania pirbuterolu jest znany z opisów patentowych St. Zj. Am. nr nr 3948919 i 4031108 i obejmuje reakcje, których przebieg przedstawia schemat 2. Z opisu patentowego St. Zj. Am. nr 4011231 znana jest odmiana tego sposobu, polegajaca na wyosobnianiu prekursora pirbuterolu w postaci soli z kwasem maleinowym, a z argentynskiego opisu patentowego nr 214005 i z luksemburskiego opisu patentowego nr 79564 znana jest inna odmiana tego procesu, polegajaca na tym, ze w ostatniej fazie procesu stosuje sie hydrogenolize zamiast hydrolizy. Jednakze i ten ostatni proces nie jest dogodny, gdyz podczas wytwarzania epoksydu powstaja uciazliwe produkty uboczne w postaci siarczków. Nawet w najlepszych warunkach prowadze¬ nie hydrogenolizy, w celu usuniecia grup zabezpieczajacych i wytwarzania pirbuterolu w postaci wolnej zasady, slady siarki przedostaja sie bowiem az do ostatniej fazy reakqi i oddzialywuja niekorzystnie na katalizator. Inna wada tego procesu jest polarny charakter aminoalkoholu bedacego produktem posrednim, bowiem utrudnia on wyosobnianie tego produktu w czystej postaci.Ostatnio, w opisie patentowym St. Zj. Am. nr 4175128, ujawniono, ze pirbuterol jest równiez uzyteczny przy leczeniu przewleklej niewydolnosci krazenia.Sposób wedlug wynalazku nie ma opisanych wyzej wad znanych sposobów. Zgodnie z wynalazkiem zwia¬ zek o wzorze 1, wytwarza sie w ten sposób, ze zwiazek o wzorze 2 ogrzewa sie z wodnym roztworem aldehydu mrówkowego w obecnosci slabej zasady, w temperaturze 85—105"C, korzystnie w temperaturze wrzenia miesza¬ niny pod chlodnica zwrotna.Jako slaba zasade stosuje sie taka, która nie reaguje w znacznym stopniu z produktami wyjsciowymi i produktem nie powoduje istotnej polimeryzacji aldehydu mrówkowego. Stosuje sie w tym celu trzeciorzedowe2 130918 aminy alifatyczne, korzystnie latwo dostepna trójetyloamine. Stosowany w tym procesie produkt wyjsciowy wytwarza sie sposobem znanym z opisu patentowego St. Zj. Am. nr 3952101.Przyklad I. Chlorowodorekpirbuterolu Roztwór 0,500 g (0,00238 mola) 5-hydroksy-2-/l-hydroksy-2-III-rzed. butyloaminoetylo/ -pirydyny w 5 ml 38% wodnego roztworu aldehydu mrówkowego z dodatkiem 1 ml trójetyloaminy utrzymuje sie w stanie wrzenia pod chlodnica zwrotna w ciagu nocy, po czym dodaje sie jeszcze 5 ml roztworu aldehydu mrówkowego i kontynuuje ogrzewanie w ciagu 6 godzin. Nastepnie odparowuje sie pod zmniejszonym cisnieniem rozpuszczal¬ niki, rozpuszcza pozostalosc w malej ilosci zimnego metanolu i nasyca roztwór bezwodnym chlorowodorem.Otrzymuje sie 0,52 g (70% wydajnosci teoretycznej) chlorowodorku pirbuterolu, który topnieje z objawami rozkladu w temperaturze 174-176°C.Zastrzezenia patentowe 1. Sposób wytwarzania pirbuterolu o wzorze 1, znamienny tym, ze zwiazek o wzorze 2 ogrzewa sie z wodnym roztworem aldehydu mrówkowego w obecnosci slabej zasady. 2. Sposób wedlug zastrz. 1, znamienny tym, ze jako slaba zasade stosuje sie trzeciorzedowa amine alifatyczna, korzystnie trójetyloamine.H0CH2' Wzór 1 Wzór 2130918 C^H5CH20y^N 1.+NC,Kwas octowy H0CH2AvKV° 2 aq HCL H C6M5CH2O HOCHz OH H B,H 26 H0CH2 \^^N OH H 7 ¦ Schemat 1130918 CfiH 6' '5 (CH3)3 S3 0 H CeH5 Y 0 NK ^N^ 0 Pirbuterol Schemat 2 PracowniaPoligraficzna UP PRL. Naklad 100 egz.Cena 100 zl PL PL

Claims (1)

Zastrzezenia patentowe 1. Sposób wytwarzania pirbuterolu o wzorze 1, znamienny tym, ze zwiazek o wzorze 2 ogrzewa sie z wodnym roztworem aldehydu mrówkowego w obecnosci slabej zasady. 2. Sposób wedlug zastrz. 1, znamienny tym, ze jako slaba zasade stosuje sie trzeciorzedowa amine alifatyczna, korzystnie trójetyloamine. H0CH2' Wzór 1 Wzór 2130918 C^H5CH20y^N
1.+NC,Kwas octowy H0CH2AvKV° 2 aq HCL H C6M5CH2O HOCHz OH H B,H 26 H0CH2 \^^N OH H 7 ¦ Schemat 1130918 CfiH 6' '5 (CH3)3 S3 0 H CeH5 Y 0 NK ^N^ 0 Pirbuterol Schemat 2 PracowniaPoligraficzna UP PRL. Naklad 100 egz. Cena 100 zl PL PL
PL1982239428A 1981-02-09 1982-02-09 Process for preparing pyrbuterol PL130918B1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US23292381A 1981-02-09 1981-02-09

Publications (2)

Publication Number Publication Date
PL239428A1 PL239428A1 (en) 1983-04-25
PL130918B1 true PL130918B1 (en) 1984-09-29

Family

ID=22875140

Family Applications (4)

Application Number Title Priority Date Filing Date
PL1982235000A PL130580B1 (en) 1981-02-09 1982-02-09 Process for preparing pyrbuterol or its analogs
PL1982239427A PL130917B1 (en) 1981-02-09 1982-02-09 Process for preparing pyrbuterol
PL1982239428A PL130918B1 (en) 1981-02-09 1982-02-09 Process for preparing pyrbuterol
PL1982239426A PL130678B1 (en) 1981-02-09 1982-02-09 Process for preparing pyrbuterol or its analogs

Family Applications Before (2)

Application Number Title Priority Date Filing Date
PL1982235000A PL130580B1 (en) 1981-02-09 1982-02-09 Process for preparing pyrbuterol or its analogs
PL1982239427A PL130917B1 (en) 1981-02-09 1982-02-09 Process for preparing pyrbuterol

Family Applications After (1)

Application Number Title Priority Date Filing Date
PL1982239426A PL130678B1 (en) 1981-02-09 1982-02-09 Process for preparing pyrbuterol or its analogs

Country Status (26)

Country Link
EP (4) EP0058072A3 (pl)
JP (4) JPS57150665A (pl)
KR (1) KR860000623B1 (pl)
AR (4) AR231439A1 (pl)
AT (2) ATE21691T1 (pl)
AU (1) AU530826B2 (pl)
CA (1) CA1179677A (pl)
CS (1) CS229678B2 (pl)
DD (2) DD210034A5 (pl)
DE (2) DE3272061D1 (pl)
DK (1) DK157541C (pl)
EG (1) EG16242A (pl)
ES (4) ES509430A0 (pl)
FI (1) FI820396L (pl)
GR (1) GR75867B (pl)
GT (1) GT198273686A (pl)
IE (2) IE52326B1 (pl)
IL (1) IL64954A (pl)
NO (4) NO820371L (pl)
NZ (1) NZ199646A (pl)
PH (4) PH20622A (pl)
PL (4) PL130580B1 (pl)
PT (1) PT74397B (pl)
SU (4) SU1194273A3 (pl)
YU (3) YU42756B (pl)
ZA (1) ZA82778B (pl)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3615293A1 (de) * 1986-05-06 1987-11-12 Bayer Ag Verwendung von heteroarylethylaminen zur leistungsfoerderung bei tieren, heteroarylethylamine und verfahren zu ihrer herstellung

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3700681A (en) * 1971-02-16 1972-10-24 Pfizer 2-hydroxymethyl-3-hydroxy-6-(1-hydroxy-2-aminoethyl)pyridines
BE795937A (fr) * 1972-03-01 1973-08-27 Pepro Procede d'hydroxymethylation d'une 3-hydroxy-pyridine substituee
AR207639A1 (es) * 1973-12-26 1976-10-22 Pfizer Un procedimiento para preparar pirido (3,2-d)1,3-dioxin-6-epoxietanos y compuestos intermediarios desprovistos de actividad terapeutica
US4031108A (en) * 1974-10-09 1977-06-21 Pfizer Inc. 2-Hydroxymethyl-3-benzyloxypyridine-6-epoxyethane
US3952101A (en) * 1975-04-14 1976-04-20 Smithkline Corporation α-Amino methyl-5-hydroxy-2-pyridinemethanols

Also Published As

Publication number Publication date
DK157541C (da) 1990-06-11
AR229712A1 (es) 1983-10-31
YU201984A (en) 1985-04-30
JPS57150665A (en) 1982-09-17
JPS6059231B2 (ja) 1985-12-24
DD202544A5 (de) 1983-09-21
ES8305721A1 (es) 1983-04-16
ES518972A0 (es) 1984-03-01
YU42908B (en) 1988-12-31
YU43389B (en) 1989-06-30
EP0058071A2 (en) 1982-08-18
IL64954A (en) 1986-03-31
FI820396L (fi) 1982-08-10
IL64954A0 (en) 1982-04-30
EP0058071B1 (en) 1986-07-23
CA1179677A (en) 1984-12-18
ES8403112A1 (es) 1984-03-01
NZ199646A (en) 1985-11-08
JPS6119624B2 (pl) 1986-05-17
ES518973A0 (es) 1984-03-01
NO820371L (no) 1982-08-10
ES8403110A1 (es) 1984-03-01
IE820275L (en) 1982-08-09
GR75867B (pl) 1984-08-02
PL130580B1 (en) 1984-08-31
KR860000623B1 (ko) 1986-05-24
PL239426A1 (en) 1983-04-25
PT74397B (en) 1984-10-09
NO824274L (no) 1982-08-10
EP0058072A3 (en) 1982-08-25
AU8027182A (en) 1982-08-19
AU530826B2 (en) 1983-07-28
PL239428A1 (en) 1983-04-25
DK157541B (da) 1990-01-22
SU1250170A3 (ru) 1986-08-07
AR229373A1 (es) 1983-07-29
PH19167A (en) 1986-01-16
IE52326B1 (en) 1987-09-16
ATE21691T1 (de) 1986-09-15
JPS6059911B2 (ja) 1985-12-27
PL130917B1 (en) 1984-09-29
PH19164A (en) 1986-01-16
PL239427A1 (en) 1983-04-25
ATE20882T1 (de) 1986-08-15
EP0058069A2 (en) 1982-08-18
YU26682A (en) 1985-04-30
EP0058072A2 (en) 1982-08-18
CS229678B2 (en) 1984-06-18
EP0058069B1 (en) 1986-08-27
ZA82778B (en) 1983-01-26
EP0058070A3 (en) 1982-08-25
KR830009028A (ko) 1983-12-17
SU1217253A3 (ru) 1986-03-07
YU201884A (en) 1985-04-30
SU1240354A3 (ru) 1986-06-23
DD210034A5 (de) 1984-05-30
PH20622A (en) 1987-03-06
JPS6135184B2 (pl) 1986-08-12
NO824275L (no) 1982-08-10
DE3272793D1 (en) 1986-10-02
YU42756B (en) 1988-12-31
AR231439A1 (es) 1984-11-30
PT74397A (en) 1982-03-01
PL130678B1 (en) 1984-08-31
SU1194273A3 (ru) 1985-11-23
DE3272061D1 (en) 1986-08-28
ES518971A0 (es) 1984-03-01
GT198273686A (es) 1983-07-30
JPS6193164A (ja) 1986-05-12
EP0058070A2 (en) 1982-08-18
PL235000A1 (en) 1983-04-11
IE820273L (en) 1982-08-09
DK52182A (da) 1982-09-17
EG16242A (en) 1989-01-30
ES509430A0 (es) 1983-04-16
AR229374A1 (es) 1983-07-29
ES8403111A1 (es) 1984-03-01
EP0058071A3 (en) 1982-08-25
IE52325B1 (en) 1987-09-16
JPS60208964A (ja) 1985-10-21
NO824273L (no) 1982-08-10
JPS60208962A (ja) 1985-10-21
PH20292A (en) 1986-11-18
EP0058069A3 (en) 1982-09-01

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