UY25524A1 - METHOD FOR PREPARING SUBSTITUTED 4-PHENYL4-CIANOCICLOHEXANOIC ACIDS - Google Patents

METHOD FOR PREPARING SUBSTITUTED 4-PHENYL4-CIANOCICLOHEXANOIC ACIDS

Info

Publication number
UY25524A1
UY25524A1 UY25524A UY25524A UY25524A1 UY 25524 A1 UY25524 A1 UY 25524A1 UY 25524 A UY25524 A UY 25524A UY 25524 A UY25524 A UY 25524A UY 25524 A1 UY25524 A1 UY 25524A1
Authority
UY
Uruguay
Prior art keywords
hydrogen
precipitate
acid
acids
cyclopentyloxy
Prior art date
Application number
UY25524A
Other languages
Spanish (es)
Inventor
Jian-Hoa Chen
Wilford Mendelson
Kevin Webb
Original Assignee
Smithkline Beecham Corp
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 Smithkline Beecham Corp filed Critical Smithkline Beecham Corp
Publication of UY25524A1 publication Critical patent/UY25524A1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D303/00Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
    • C07D303/02Compounds containing oxirane rings
    • C07D303/48Compounds containing oxirane rings with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms, e.g. ester or nitrile radicals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/06Antiasthmatics
    • 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
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C255/00Carboxylic acid nitriles
    • C07C255/45Carboxylic acid nitriles having cyano groups bound to carbon atoms of rings other than six-membered aromatic rings
    • C07C255/46Carboxylic acid nitriles having cyano groups bound to carbon atoms of rings other than six-membered aromatic rings to carbon atoms of non-condensed rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/61Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
    • C07C45/67Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
    • C07C45/68Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
    • C07C45/70Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction with functional groups containing oxygen only in singly bound form
    • C07C45/71Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction with functional groups containing oxygen only in singly bound form being hydroxy groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C47/00Compounds having —CHO groups
    • C07C47/52Compounds having —CHO groups bound to carbon atoms of six—membered aromatic rings
    • C07C47/575Compounds having —CHO groups bound to carbon atoms of six—membered aromatic rings containing ether groups, groups, groups, or groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00Systems containing only non-condensed rings
    • C07C2601/06Systems containing only non-condensed rings with a five-membered ring
    • C07C2601/08Systems containing only non-condensed rings with a five-membered ring the ring being saturated
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00Systems containing only non-condensed rings
    • C07C2601/12Systems containing only non-condensed rings with a six-membered ring
    • C07C2601/14The ring being saturated

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Pulmonology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (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)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Método para sintetizar compuestos de fórmula (I) representada en la figura 1, dond: R' y R'' son independientemente hidrógeno o -C(O)OX, siendo X hidrógeno o un catión metálico o amonio; R3 es hidrógeno, halógeno, alquilo, CH2NHC(O)C(O)NH2, ciclopropilo; X2 es O o NR8, siendo R8 hidrógeno o alquilo C1-C4 opcionalmente sustituid con uno a tres átomos de flúor; el método comprende combinar un haluro de un alcalino o alcalinotérreo con un disolvente aprótico dipolar, básicamente amídico, agua y uno de los compuestos representados en la figura 2 (particularmente el cis-6-[3-(ciclopentiloxi)-4-metoxifenil)]-1-oxaespiro[2,5]octano-2,6-dicarbonitrilo), y calentar la combinación a una temperatura de al menos aproximadamente 60s durante varias horas, opcionalmente en una atmósfera inerte, precipitar un compuesto de fórmula (I) por adición de una base fuerte a dicha combinación, luego retirar el disolvente básicamente amídico y el agua de dicho precipitado, y opcionalmente purificar aún más el precipitado, o acidular el precipitado para obtener el ácido libre. En especial se incluyen compuestos intermedios y a una ruta sintética para obtener ácido 4-ciano-4-(3-ciclopentiloxi-4-metoxifenil)ciclohexanoico y sus análogos. Este ácido y sus análogos nombrados son selectivos inhibidores del sitio catalítico en la isoenzima fosfodiesterasa denominada IV ("PDE IV") y por ello los ácidos son útiles en el tratamiento de ciertas enfermedades que se pueden aliviar afectando a la enzima PDE IV y sus subtipos.Method for synthesizing compounds of formula (I) represented in figure 1, where: R 'and R' 'are independently hydrogen or -C (O) OX, where X is hydrogen or a metal or ammonium cation; R3 is hydrogen, halogen, alkyl, CH2NHC (O) C (O) NH2, cyclopropyl; X2 is O or NR8, with R8 being hydrogen or C1-C4 alkyl optionally substituted with one to three fluorine atoms; the method comprises combining a halide of an alkaline or alkaline earth with a dipolar aprotic solvent, basically amidic, water and one of the compounds represented in figure 2 (particularly cis-6- [3- (cyclopentyloxy) -4-methoxyphenyl)] -1-oxaspiro [2,5] octano-2,6-dicarbonitrile), and heating the combination to a temperature of at least about 60s for several hours, optionally in an inert atmosphere, precipitating a compound of formula (I) by addition from a strong base to said combination, then remove basically amidic solvent and water from said precipitate, and optionally further purify the precipitate, or acidify the precipitate to obtain the free acid. In particular, intermediate compounds and a synthetic route to obtain 4-cyano-4- (3-cyclopentyloxy-4-methoxyphenyl) cyclohexanoic acid and its analogs are included. This acid and its named analogues are selective inhibitors of the catalytic site in the isoenzyme phosphodiesterase called IV ("PDE IV") and therefore the acids are useful in the treatment of certain diseases that can be alleviated by affecting the enzyme PDE IV and its subtypes .

UY25524A 1997-10-10 1999-05-25 METHOD FOR PREPARING SUBSTITUTED 4-PHENYL4-CIANOCICLOHEXANOIC ACIDS UY25524A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US6161397P 1997-10-10 1997-10-10

Publications (1)

Publication Number Publication Date
UY25524A1 true UY25524A1 (en) 2000-02-23

Family

ID=22036929

Family Applications (2)

Application Number Title Priority Date Filing Date
UY25201A UY25201A1 (en) 1997-10-10 1998-10-07 METHOD FOR TREATING SUBSTITUTED 4-PHENYL-4-CYANOCICLOHEXANOIC ACID
UY25524A UY25524A1 (en) 1997-10-10 1999-05-25 METHOD FOR PREPARING SUBSTITUTED 4-PHENYL4-CIANOCICLOHEXANOIC ACIDS

Family Applications Before (1)

Application Number Title Priority Date Filing Date
UY25201A UY25201A1 (en) 1997-10-10 1998-10-07 METHOD FOR TREATING SUBSTITUTED 4-PHENYL-4-CYANOCICLOHEXANOIC ACID

Country Status (30)

Country Link
EP (1) EP1043930A4 (en)
JP (1) JP2001519363A (en)
KR (1) KR100560038B1 (en)
CN (1) CN1192025C (en)
AP (1) AP1335A (en)
AR (1) AR015952A1 (en)
AU (1) AU741832B2 (en)
BG (1) BG104302A (en)
BR (1) BR9814064A (en)
CA (1) CA2305614A1 (en)
DZ (1) DZ2619A1 (en)
EA (1) EA003609B1 (en)
HU (1) HUP0003905A3 (en)
ID (1) ID25536A (en)
IL (1) IL135434A (en)
MA (1) MA24670A1 (en)
MY (1) MY122105A (en)
NO (1) NO20001777L (en)
NZ (1) NZ503759A (en)
OA (1) OA11347A (en)
PE (1) PE121599A1 (en)
PL (1) PL191974B1 (en)
SA (1) SA99191000A (en)
SK (1) SK4902000A3 (en)
TR (1) TR200000945T2 (en)
TW (1) TW440557B (en)
UA (1) UA67753C2 (en)
UY (2) UY25201A1 (en)
WO (1) WO1999018793A1 (en)
ZA (1) ZA989228B (en)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9920152D0 (en) * 1999-08-25 1999-10-27 Smithkline Beecham Plc Novel process
EP1237851A4 (en) * 1999-12-15 2004-06-23 Smithkline Beecham SALTS OF i Cis /i -4-CYANO-4- 3-(CYCLOPENTYLOXY)-4-METHOXYPHENYL]CYCLOHEXANE-1-CARBOXYLIC ACID
WO2001055094A1 (en) * 2000-01-26 2001-08-02 Smithkline Beecham Corporation Monohydrate of cis-lithium-cyano-4-[3-(cyclopentyloxy)-4-methoxyphenyl]cyclohexanecarboxylate
EP1265861A2 (en) 2000-03-16 2002-12-18 Inflazyme Pharmaceuticals, Ltd. Benzylated pde4 inhibitors
US7250518B2 (en) 2001-01-31 2007-07-31 Pfizer Inc. Nicotinamide acids, amides, and their mimetics active as inhibitors of PDE4 isozymes
BR0116845A (en) 2001-01-31 2004-02-25 Pfizer Prod Inc Ether derivatives useful as pde4 isozyme inhibitors
BR0116852A (en) 2001-01-31 2004-02-25 Pfizer Prod Inc Biarylated nicotinamide derivatives useful as pde4 isozyme inhibitors
EA200300622A1 (en) 2001-01-31 2003-12-25 Пфайзер Продактс Инк. DERIVATIVES OF AMIDES TIAZOLYL-, OXAZOLYL, PYRROLYL-AND IMIDAZOZYL ACID, USEFUL AS AN INHIBITORS OF PDE4 ISOFERMENT
CN102491959B (en) * 2011-12-19 2015-03-25 江苏澄扬作物科技有限公司 Preparation method of oxirane derivative

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4021478A (en) * 1972-07-13 1977-05-03 The Upjohn Company Preparation of carboxylic acids from glycidonitriles with ionic lewis acids
SK279958B6 (en) * 1992-04-02 1999-06-11 Smithkline Beecham Corporation Compounds exhibiting anti-allergic and anti-inflammatory properties, pharmaceutical composition them containing and their use
US5524438A (en) * 1994-12-15 1996-06-11 United Technologies Corporation Segmented bulkhead liner for a gas turbine combustor
UY24882A1 (en) * 1997-02-12 2001-08-27 Smithkline Beecham Corp SUBSTITUTED 4-PHENYL-4-CIANO-CYCLOHEXANOIC ACIDS
US6452022B1 (en) * 1997-10-10 2002-09-17 Smithkline Beecham Corporation Method for preparing substituted 4-phenyl-4-cyanocyclohexanoic acids

Also Published As

Publication number Publication date
AU9687498A (en) 1999-05-03
OA11347A (en) 2003-12-17
TW440557B (en) 2001-06-16
AU741832B2 (en) 2001-12-13
JP2001519363A (en) 2001-10-23
PL191974B1 (en) 2006-07-31
HUP0003905A3 (en) 2002-01-28
UY25201A1 (en) 2001-08-27
UA67753C2 (en) 2004-07-15
MA24670A1 (en) 1999-07-01
EP1043930A1 (en) 2000-10-18
DZ2619A1 (en) 2003-03-08
EA003609B1 (en) 2003-06-26
CN1192025C (en) 2005-03-09
EP1043930A4 (en) 2004-09-15
AP2000001782A0 (en) 2000-06-30
BG104302A (en) 2001-08-31
NO20001777D0 (en) 2000-04-06
ZA989228B (en) 1999-04-12
IL135434A0 (en) 2001-05-20
CN1275052A (en) 2000-11-29
AP1335A (en) 2004-11-29
KR20010015709A (en) 2001-02-26
NO20001777L (en) 2000-05-03
PE121599A1 (en) 2000-02-19
SK4902000A3 (en) 2000-11-07
CA2305614A1 (en) 1999-04-22
AR015952A1 (en) 2001-05-30
EA200000406A1 (en) 2000-10-30
BR9814064A (en) 2000-09-26
PL339759A1 (en) 2001-01-02
SA99191000A (en) 2005-12-03
NZ503759A (en) 2002-03-01
HUP0003905A2 (en) 2001-03-28
KR100560038B1 (en) 2006-03-13
IL135434A (en) 2004-12-15
ID25536A (en) 2000-10-12
TR200000945T2 (en) 2000-10-23
MY122105A (en) 2006-03-31
WO1999018793A1 (en) 1999-04-22

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Effective date: 20110817