UA26400C2 - Спосіб одержаhhя похідhого ерголіhу - Google Patents

Спосіб одержаhhя похідhого ерголіhу

Info

Publication number
UA26400C2
UA26400C2 UA93003963A UA93003963A UA26400C2 UA 26400 C2 UA26400 C2 UA 26400C2 UA 93003963 A UA93003963 A UA 93003963A UA 93003963 A UA93003963 A UA 93003963A UA 26400 C2 UA26400 C2 UA 26400C2
Authority
UA
Ukraine
Prior art keywords
formula
ergolich
ergolin
derivative
obtaining derivative
Prior art date
Application number
UA93003963A
Other languages
English (en)
Russian (ru)
Inventor
Іларіа Кандіані
Илариа Кандиани
Уолтер Кабрі
Уолтер Кабри
Анжело Бедескі
Анжело Бедески
Франко Заріні
Франко Зарини
Original Assignee
Фарміталіа Карло Ерба С.Р.Л.
Фармиталиа Карло Эрба С.Р.Л.
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 Фарміталіа Карло Ерба С.Р.Л., Фармиталиа Карло Эрба С.Р.Л. filed Critical Фарміталіа Карло Ерба С.Р.Л.
Publication of UA26400C2 publication Critical patent/UA26400C2/uk

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D457/00Heterocyclic compounds containing indolo [4, 3-f, g] quinoline ring systems, e.g. derivatives of ergoline, of the formula:, e.g. lysergic acid
    • C07D457/04Heterocyclic compounds containing indolo [4, 3-f, g] quinoline ring systems, e.g. derivatives of ergoline, of the formula:, e.g. lysergic acid 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 in position 8
    • C07D457/06Lysergic acid amides
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/14Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • A61P25/16Anti-Parkinson drugs
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P5/00Drugs for disorders of the endocrine system
    • A61P5/06Drugs for disorders of the endocrine system of the anterior pituitary hormones, e.g. TSH, ACTH, FSH, LH, PRL, GH
    • A61P5/08Drugs for disorders of the endocrine system of the anterior pituitary hormones, e.g. TSH, ACTH, FSH, LH, PRL, GH for decreasing, blocking or antagonising the activity of the anterior pituitary hormones

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Neurology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Neurosurgery (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Biomedical Technology (AREA)
  • Diabetes (AREA)
  • Endocrinology (AREA)
  • Psychology (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Emergency Protection Circuit Devices (AREA)
  • Control Of Electric Motors In General (AREA)

Abstract

Винахід стосується способу одержання похідного ерголіну формули (l): де R1 представляє етильну групу, R2 представляє диметиламінопропільну групу (CH3)2N(CH2)3, R3 представляє алліл, R4 і R5 представляють атом водню. Зазначену речовину одержують при взаємодії аміду ерголіну формули (ll) з 1-4 еквівалентами ізоціанату формули (lll): Реакцію проводять в розчиннику, такому як діхлорметан, 1,1-діхлоретан або толуол, при температурі від 35°C до 60°C, у присутності CuCI або CuCI2 і сполуки фосфору, вибраної поміж PPh3, P(n-CIPh)3, P(n-MePh)3 і MePh2P.
UA93003963A 1992-03-12 1993-02-15 Спосіб одержаhhя похідhого ерголіhу UA26400C2 (uk)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB929205439A GB9205439D0 (en) 1992-03-12 1992-03-12 Process for the synthesis of ergoline derivatives
PCT/EP1993/000360 WO1993018034A1 (en) 1992-03-12 1993-02-15 Process for the preparation of ergoline derivatives

Publications (1)

Publication Number Publication Date
UA26400C2 true UA26400C2 (uk) 1999-08-30

Family

ID=10712024

Family Applications (1)

Application Number Title Priority Date Filing Date
UA93003963A UA26400C2 (uk) 1992-03-12 1993-02-15 Спосіб одержаhhя похідhого ерголіhу

Country Status (25)

Country Link
US (1) US5382669A (uk)
EP (1) EP0593692B1 (uk)
JP (1) JP3339858B2 (uk)
KR (1) KR100274102B1 (uk)
CN (1) CN1038510C (uk)
AT (1) ATE180783T1 (uk)
AU (1) AU653099B2 (uk)
CA (1) CA2106371C (uk)
CZ (1) CZ281708B6 (uk)
DE (1) DE69325138D1 (uk)
FI (1) FI113473B (uk)
GB (1) GB9205439D0 (uk)
HU (1) HU210407B (uk)
IL (1) IL104973A (uk)
MX (1) MX9301297A (uk)
MY (1) MY109152A (uk)
NO (1) NO302754B1 (uk)
NZ (1) NZ249115A (uk)
PH (1) PH30138A (uk)
RU (1) RU2118323C1 (uk)
SK (1) SK279039B6 (uk)
TW (1) TW215089B (uk)
UA (1) UA26400C2 (uk)
WO (1) WO1993018034A1 (uk)
ZA (1) ZA931720B (uk)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0007308D0 (en) 2000-03-24 2000-05-17 Pharmacia & Upjohn Spa Process for preparing crystalline form | of cabergoline
US6696568B2 (en) 2001-04-16 2004-02-24 Finetech Ltd. Process and intermediates for production of cabergoline and related compounds
IL155545A (en) * 2003-04-21 2009-12-24 Finetech Pharmaceutical Ltd Solvate form of cabergoline
HUP0400517A3 (en) * 2004-03-04 2006-05-29 Richter Gedeon Vegyeszet Process for producing cabergoline
GB0409785D0 (en) * 2004-04-30 2004-06-09 Resolution Chemicals Ltd Preparation of cabergoline
FR2877945A1 (fr) * 2004-11-18 2006-05-19 Archemis Sa Procede de la preparation de la cabergoline
EP1858894A1 (en) 2005-03-17 2007-11-28 Synthon Argentina S.A. Improved process for making cabergoline
GB0505965D0 (en) * 2005-03-23 2005-04-27 Resolution Chemicals Ltd Preparation of cabergoline
EP1925616A1 (en) * 2006-10-26 2008-05-28 LEK Pharmaceuticals D.D. Process for the preparation of crystal forms of cabergoline via stable solvates of cabergoline
US7939665B2 (en) * 2007-05-04 2011-05-10 Apotex Pharmachem Inc. Efficient process for the preparation of cabergoline and its intermediates
WO2014078857A1 (en) 2012-11-19 2014-05-22 Regents Of The University Of Minnesota Ergoline derivatives as dopamine receptor modulators

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2103603B (en) * 1981-08-11 1985-04-11 Erba Farmitalia Ergoline derivatives

Also Published As

Publication number Publication date
SK140193A3 (en) 1994-11-09
EP0593692B1 (en) 1999-06-02
HUT66712A (en) 1994-12-28
HU210407B (en) 1995-04-28
KR100274102B1 (ko) 2000-12-15
JP3339858B2 (ja) 2002-10-28
NO934077L (no) 1993-11-11
IL104973A (en) 1997-06-10
ZA931720B (en) 1993-11-01
CA2106371A1 (en) 1993-09-13
GB9205439D0 (en) 1992-04-22
MY109152A (en) 1996-12-31
TW215089B (uk) 1993-10-21
NZ249115A (en) 1995-04-27
AU653099B2 (en) 1994-09-15
CZ281708B6 (cs) 1996-12-11
FI113473B (fi) 2004-04-30
CZ271593A3 (en) 1994-04-13
WO1993018034A1 (en) 1993-09-16
MX9301297A (es) 1993-09-01
NO934077D0 (no) 1993-11-11
DE69325138D1 (de) 1999-07-08
AU3497493A (en) 1993-10-05
CN1076196A (zh) 1993-09-15
IL104973A0 (en) 1993-07-08
US5382669A (en) 1995-01-17
JPH06507648A (ja) 1994-09-01
RU2118323C1 (ru) 1998-08-27
EP0593692A1 (en) 1994-04-27
SK279039B6 (sk) 1998-05-06
NO302754B1 (no) 1998-04-20
PH30138A (en) 1997-01-21
FI934933A0 (fi) 1993-11-08
CN1038510C (zh) 1998-05-27
FI934933A (fi) 1993-11-08
CA2106371C (en) 2003-09-23
ATE180783T1 (de) 1999-06-15

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