IL111030A - Phenyl-alkyl alcohol esters are converted to position 2 - Google Patents

Phenyl-alkyl alcohol esters are converted to position 2

Info

Publication number
IL111030A
IL111030A IL11103091A IL11103091A IL111030A IL 111030 A IL111030 A IL 111030A IL 11103091 A IL11103091 A IL 11103091A IL 11103091 A IL11103091 A IL 11103091A IL 111030 A IL111030 A IL 111030A
Authority
IL
Israel
Prior art keywords
water
equiv
preparation
added
washed
Prior art date
Application number
IL11103091A
Other languages
English (en)
Hebrew (he)
Original Assignee
Smith Kline French Lab
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 Smith Kline French Lab filed Critical Smith Kline French Lab
Publication of IL111030A publication Critical patent/IL111030A/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C205/00Compounds containing nitro groups bound to a carbon skeleton
    • C07C205/39Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by esterified hydroxy groups
    • C07C205/40Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by esterified hydroxy groups having nitro groups and esterified hydroxy groups bound to acyclic carbon atoms of the carbon skeleton
    • 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
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/08Vasodilators for multiple indications
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C201/00Preparation of esters of nitric or nitrous acid or of compounds containing nitro or nitroso groups bound to a carbon skeleton
    • C07C201/06Preparation of nitro compounds
    • C07C201/12Preparation of nitro compounds by reactions not involving the formation of nitro groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/76Esters of carboxylic acids having a carboxyl group bound to a carbon atom of a six-membered aromatic ring
    • C07C69/78Benzoic acid esters
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04Indoles; Hydrogenated indoles
    • C07D209/30Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
    • C07D209/32Oxygen atoms
    • C07D209/34Oxygen atoms in position 2

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Cardiology (AREA)
  • Urology & Nephrology (AREA)
  • Vascular Medicine (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Indole Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Hydrogenated Pyridines (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
IL11103091A 1990-04-17 1991-04-16 Phenyl-alkyl alcohol esters are converted to position 2 IL111030A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB909008605A GB9008605D0 (en) 1990-04-17 1990-04-17 Process
IL9786791A IL97867A (en) 1990-04-17 1991-04-16 Process for making indolones and intermediates used in it

Publications (1)

Publication Number Publication Date
IL111030A true IL111030A (en) 1995-11-27

Family

ID=10674534

Family Applications (7)

Application Number Title Priority Date Filing Date
IL11103091A IL111030A (en) 1990-04-17 1991-04-16 Phenyl-alkyl alcohol esters are converted to position 2
IL11102991A IL111029A (en) 1990-04-17 1991-04-16 Esters of 4-hydroxyalkyl-indoline-2-helium
IL11102891A IL111028A (en) 1990-04-17 1991-04-16 4-Hydroxyalkyl- Indole-2-Onim
IL9786791A IL97867A (en) 1990-04-17 1991-04-16 Process for making indolones and intermediates used in it
IL11102894A IL111028A0 (en) 1990-04-17 1994-09-22 Intermediates to indolones
IL11102994A IL111029A0 (en) 1990-04-17 1994-09-22 Intermediates to indolones
IL11103094A IL111030A0 (en) 1990-04-17 1994-09-22 Intermediates to indolones

Family Applications After (6)

Application Number Title Priority Date Filing Date
IL11102991A IL111029A (en) 1990-04-17 1991-04-16 Esters of 4-hydroxyalkyl-indoline-2-helium
IL11102891A IL111028A (en) 1990-04-17 1991-04-16 4-Hydroxyalkyl- Indole-2-Onim
IL9786791A IL97867A (en) 1990-04-17 1991-04-16 Process for making indolones and intermediates used in it
IL11102894A IL111028A0 (en) 1990-04-17 1994-09-22 Intermediates to indolones
IL11102994A IL111029A0 (en) 1990-04-17 1994-09-22 Intermediates to indolones
IL11103094A IL111030A0 (en) 1990-04-17 1994-09-22 Intermediates to indolones

Country Status (29)

Country Link
US (1) US5336781A (de)
EP (1) EP0526529B1 (de)
JP (2) JP2788548B2 (de)
KR (1) KR0180215B1 (de)
CN (1) CN1027892C (de)
AP (1) AP184A (de)
AT (1) ATE144251T1 (de)
AU (2) AU640006B2 (de)
CA (1) CA2080221C (de)
CY (1) CY1981A (de)
DE (1) DE69122753T2 (de)
DK (1) DK0526529T3 (de)
ES (1) ES2094812T3 (de)
FI (1) FI101148B (de)
GB (1) GB9008605D0 (de)
GR (1) GR3022261T3 (de)
HK (1) HK3097A (de)
HU (1) HU214822B (de)
IE (1) IE911262A1 (de)
IL (7) IL111030A (de)
MA (1) MA22133A1 (de)
MY (1) MY109628A (de)
NO (2) NO178396C (de)
NZ (1) NZ237819A (de)
PL (1) PL166736B1 (de)
PT (1) PT97375B (de)
SA (1) SA91110352B1 (de)
WO (1) WO1991016306A1 (de)
ZA (1) ZA912782B (de)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9008605D0 (en) * 1990-04-17 1990-06-13 Smith Kline French Lab Process
DE69131775T2 (de) * 1990-09-28 2000-04-20 Smithkline Beecham Corp. Verfahren zur Herstellung wasserlöslicher Camptothecinanaloge, sowie die Verbindungen 10-Hydroxy-11-C(1-6)-alkoxycamptothecin
GB9300309D0 (en) * 1993-01-08 1993-03-03 Smithkline Beecham Plc Process
US6218421B1 (en) * 1999-07-01 2001-04-17 Smithkline Beecham P.L.C. Method of promoting smoking cessation
AR030557A1 (es) 2000-04-14 2003-08-27 Jagotec Ag Una tableta en multicapa de liberacion controlada y metodo de tratamiento
WO2005074387A2 (en) * 2003-12-30 2005-08-18 Sun Pharmaceutical Industries Limited Novel crystal forms of 4-[2-di-n-propylamino)ethyl]-2 (3h)- indolone hydrochloride
US7378439B2 (en) * 2004-01-20 2008-05-27 Usv, Ltd. Process for the preparation of 4-(2-dipropylaminoethyl)-1,3-dihydro-2H-indol-2-one hydrochloride
WO2005105741A1 (en) * 2004-02-11 2005-11-10 Sun Pharmaceutical Industries Limited Substantially pure 4-[2-(di-n-propylamino)ethyl]-2(3h)-indolone hydrochloride
WO2005080333A1 (en) * 2004-02-19 2005-09-01 Torrent Pharmaceuticals Ltd Process for purification of ropinirole
US20070254941A1 (en) * 2006-04-21 2007-11-01 Glenmark Pharmaceuticals Limited Subtantially pure ropinirole hydrochloride, polymorphic form of ropinirole and process for their preparation
CN103130704B (zh) * 2013-03-11 2019-03-22 上海奥博生物医药技术有限公司 一种制备4-(2-羟乙基)-1,3-二氢-2h-吲哚-2-酮的新方法
CN103145604A (zh) * 2013-03-19 2013-06-12 上海奥博生物医药技术有限公司 一种制备罗匹尼罗关键中间体的方法
CN105418482A (zh) * 2015-11-23 2016-03-23 东南大学 一种改进的盐酸罗匹尼罗的制备方法
CN108440376B (zh) * 2018-05-08 2020-06-05 中国科学院成都生物研究所 一种盐酸罗匹尼罗的制备方法

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1154976A (en) * 1967-02-21 1969-06-11 Pfizer Ltd N-Phenyl Indoline Derivatives
JPS53101333A (en) * 1977-02-14 1978-09-04 Sagami Chem Res Center 3-acyloxymethyl-3,4:5,6-diepoxycyclohexane-1,2-diol and
IT1171624B (it) * 1980-11-12 1987-06-10 Thomae Gmbh Dr K Indolinoni dotati di proprieta' farmaceutiche e procedimento per la loro produzione
US4588790A (en) * 1982-03-24 1986-05-13 Union Carbide Corporation Method for fluidized bed polymerization
US4452808A (en) * 1982-12-07 1984-06-05 Smithkline Beckman Corporation 4-Aminoalkyl-2(3H)-indolones
US4593033A (en) * 1985-04-24 1986-06-03 Merck & Co., Inc. Substituted indeno[2,1-c] pyridines useful as calcium channel blockers
GB8712073D0 (en) * 1987-05-21 1987-06-24 Smith Kline French Lab Medicament
GB8714371D0 (en) * 1987-06-19 1987-07-22 Smith Kline French Lab Process
FR2635104B1 (fr) * 1988-08-03 1992-04-30 Synthelabo Derives d'indolone, leur preparation et leur application en therapeutique
GB9008605D0 (en) * 1990-04-17 1990-06-13 Smith Kline French Lab Process

Also Published As

Publication number Publication date
KR0180215B1 (ko) 1999-03-20
NO178396C (no) 1996-03-20
WO1991016306A1 (en) 1991-10-31
AU640006B2 (en) 1993-08-12
IL111029A (en) 1995-11-27
US5336781A (en) 1994-08-09
GR3022261T3 (en) 1997-04-30
FI924674A0 (fi) 1992-10-15
HUT64742A (en) 1994-02-28
PL166736B1 (pl) 1995-06-30
DK0526529T3 (da) 1996-11-18
NO1999012I1 (no) 1999-06-18
EP0526529A1 (de) 1993-02-10
CY1981A (en) 1997-09-05
PT97375A (pt) 1992-01-31
HK3097A (en) 1997-01-10
IL111029A0 (en) 1994-11-28
EP0526529B1 (de) 1996-10-16
ZA912782B (en) 1992-11-25
SA91110352B1 (ar) 2001-11-12
NO924028L (no) 1992-10-16
AU3566993A (en) 1993-06-03
ATE144251T1 (de) 1996-11-15
CA2080221A1 (en) 1991-10-18
CN1056686A (zh) 1991-12-04
AP184A (en) 1992-06-30
CA2080221C (en) 2000-11-14
AU646771B2 (en) 1994-03-03
JPH05506029A (ja) 1993-09-02
DE69122753T2 (de) 1997-05-07
PT97375B (pt) 1998-08-31
FI924674A (fi) 1992-10-15
HU9203261D0 (en) 1992-12-28
NO178396B (no) 1995-12-11
DE69122753D1 (de) 1996-11-21
HU214822B (hu) 1998-06-29
IL111028A (en) 1995-11-27
JP3044013B2 (ja) 2000-05-22
AU7656291A (en) 1991-11-11
AP9100251A0 (en) 1991-04-30
IL97867A (en) 1995-11-27
IL111028A0 (en) 1994-11-28
IL97867A0 (en) 1992-06-21
ES2094812T3 (es) 1997-02-01
JP2788548B2 (ja) 1998-08-20
IE911262A1 (en) 1991-10-23
MY109628A (en) 1997-03-31
FI101148B (fi) 1998-04-30
NZ237819A (en) 1993-05-26
JPH10251205A (ja) 1998-09-22
GB9008605D0 (en) 1990-06-13
IL111030A0 (en) 1994-11-28
MA22133A1 (fr) 1991-12-31
CN1027892C (zh) 1995-03-15
NO924028D0 (no) 1992-10-16

Similar Documents

Publication Publication Date Title
KR101461291B1 (ko) 약학적 활성 화합물의 제조 방법
EP0526529B1 (de) Ein verbessertes verfahren zur herstellung von substituierten indolone derivaten
CZ283215B6 (cs) Způsob výroby 3-(alfa-methyxy)methylenbenzofuranonů
JP2846042B2 (ja) インドールカルボン酸誘導体の製造法
USRE27592E (en) Chxchjxx
DK149230B (da) Analogifremgangsmaade til fremstilling af 5-benzoyl-6-hydroxy-indan-1-carboxylsyrederivater eller farmaceutisk acceptable salte deraf
Jackson et al. The synthesis of indolyl-butyric acid and some of its derivatives
NO157637B (no) Gelformig anode og elektrokjemisk celle inneholdende denne
US3933818A (en) Heterocyclic compounds
JP2622135B2 (ja) インデン誘導体及びその製造方法
EP0238411A1 (de) 1,2-Dihydro-4-methyl-1-oxo-5H-pyrido(4,3-b)-Indole und ihre Herstellung
NZ242374A (en) Phenyl alkyl ester compounds useful as intermediates in the preparation of 4-(aminoalkyl)-1,3-dihydro-2h-indol-2-one derivatives
US4009172A (en) 2,3,3A,6,7,7A-Hexahydro-thieno[3,2-b]pyridin-(4H)5-ones
US3972883A (en) 1,6-Dimethyl-8β-[2' or 3'-pyrroyloxyethyl or substituted pyrroyloxyethyl]-10α-methoxyergolene compounds
JPH09176167A (ja) フィソスチグミンからフィソスチグミンカルバメート誘導体を製造する方法
IE42956B1 (en) 4-amino-3-pyrrole carboxamides
US5153330A (en) Thiapentanamide derivatives
US4543415A (en) Process for preparing tricyclic indoles
US4140687A (en) Process for the preparation of 8-halodihydrocodeinone hydrohalides and codeine
NO123526B (de)
US3551476A (en) 3-(hydroxyphenyl)-4-aminovalerates
SU528871A3 (ru) Способ получени производных 2-(1н) -хиназолинона
WO1982002044A1 (en) Preparation of pyrrole esters
Dagger et al. JD Hayler, SLB Howie, RG Giles*, A. Negus, PW Oxley, TC Walsgrove*, and SE Walsh
JPH0136825B2 (de)

Legal Events

Date Code Title Description
FF Patent granted
KB Patent renewed
RH Patent void
KB Patent renewed
KB Patent renewed
KB Patent renewed
EXP Patent expired