MY121795A - Synthesis of intermediates useful in preparing tricyclic compounds - Google Patents
Synthesis of intermediates useful in preparing tricyclic compoundsInfo
- Publication number
- MY121795A MY121795A MYPI99005048A MYPI9905048A MY121795A MY 121795 A MY121795 A MY 121795A MY PI99005048 A MYPI99005048 A MY PI99005048A MY PI9905048 A MYPI9905048 A MY PI9905048A MY 121795 A MY121795 A MY 121795A
- Authority
- MY
- Malaysia
- Prior art keywords
- formula
- compound
- preparing
- heteroaryl
- alkoxy
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D221/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00
- C07D221/02—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00 condensed with carbocyclic rings or ring systems
- C07D221/04—Ortho- or peri-condensed ring systems
- C07D221/06—Ring systems of three rings
- C07D221/16—Ring systems of three rings containing carbocyclic rings other than six-membered
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pyridine Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
DISCLOSED IS A PROCESS FOR PREPARING A COMPOUND HAVING THE FORMULA: FORMULA I WHEREIN R, R1, R2, R3, AND R4 ARE INDEPENDENTLY SELECTED FROM THE GROUPCONSISTING OF H, BR, C1, F, ALKYL, OR ALKOXY, BY(A) REACTING A COMPOUND HAVING THE FORMULA FORMULA II WHEREIN RA, RB, RC, RD, AND RE ARE INDEPENDENTLY SELECTED FROM THE GROUPCONSISTING OF H, HALO, ALKYL, OR ALKOXY, AND R5 IS ARYL OR HETEROARYL, WITH A DEHYDRATING AGENT TO PRODUCE AN IMINE HAVING THE FORMULA: FORMULA (B) HYDROLYZING THE IMINE PRODUCED IN STEP (A) TO PRODUCE THE COMPOUND HAVING FORMULA (I). ALSO DISCLOSED ARE NOVEL INTERMEDIATES HAVING THE FORMULA : FORMULA WHEREIN RA, RB, RC, RD, AND RE ARE INDEPENDENTLY SELECTED FROM THE GROUP CONSISTINGOF H, HALO, ALKYL, OR ALKOXY, AND R5 IS ARYL OR HETEROARYL. ALSO DISCLOSED IS A PROCESSFOR PREPARING A COMPOUND HAVING THE FORMULA: FORMULA III COMPRISING: REACTING A COMPOUND HAVING THE FORMULA FORMULA IV WITH NH2R5 IN THE PRESENCE OF A PALLADIUM CATALYST, CARBON MONOXIDE, A BASE, AND ANETHER SELECTED FROM THE GROUP CONSISTING OF; CH3OCH2CH2OCH3;CH3OCH2CH2OCH2CH2OCH3; AND CH3OCH2CH2OCH2CH2OCH2CH2OCH3, WHEREIN X IS H, BR, C1, OR F, AND R5 IS ARYL OR HETEROARYL. THE COMPOUNDS MADE BY THESEP ROCESSES ARE USEFUL INTERMEDIATES FOR PREPARING COMPOUNDS THAT ARE ANTIHISTAMINES ORINHIBITORS OF FARNESYL PROTEIN TRANSFERASE.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US19700398A | 1998-11-20 | 1998-11-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
MY121795A true MY121795A (en) | 2006-02-28 |
Family
ID=22727622
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MYPI99005048A MY121795A (en) | 1998-11-20 | 1999-11-19 | Synthesis of intermediates useful in preparing tricyclic compounds |
Country Status (13)
Country | Link |
---|---|
EP (1) | EP1131296A2 (en) |
JP (2) | JP4663122B2 (en) |
CN (1) | CN1162404C (en) |
AR (1) | AR028138A1 (en) |
AU (1) | AU3790200A (en) |
CA (1) | CA2351693C (en) |
CO (1) | CO5150169A1 (en) |
HK (1) | HK1038698A1 (en) |
MY (1) | MY121795A (en) |
PE (1) | PE20001243A1 (en) |
TW (1) | TW509680B (en) |
WO (1) | WO2000030589A2 (en) |
ZA (1) | ZA200103246B (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU2001253602A1 (en) * | 2000-04-18 | 2001-10-30 | Schering Corporation | Synthesis of intermediates useful in preparing tricyclic compounds |
WO2004058719A1 (en) * | 2002-12-26 | 2004-07-15 | Cadila Healthcare Limited | A process for preparing benzocyclohetapyridin-11-ones |
CN108218773A (en) * | 2018-02-28 | 2018-06-29 | 朱路英 | A kind of method for preparing resisting allergic rhinitis drug loratadine intermedite |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4282233B1 (en) | 1980-06-19 | 2000-09-05 | Schering Corp | Antihistaminic 11-(4-piperidylidene)-5h-benzoÄ5,6Ü-cyclohepta-Ä1,2Ü-pyridines |
US4731447A (en) * | 1985-05-13 | 1988-03-15 | Schering Corporation | Process for preparing piperidylidene dihydro-dibenzo(a,d)-cycloheptenes or aza-derivatives thereof |
EP0208855B1 (en) * | 1985-05-13 | 1991-03-06 | Schering Corporation | process for preparing piperidylidene dihydrodibenzo(a,d)cycloheptenes and aza derivatives thereof, compounds obtained by such process and the use of such compounds for preparing useful pharmaceutical compositions |
US5089496A (en) | 1986-10-31 | 1992-02-18 | Schering Corporation | Benzo[5,6]cycloheptapyridine compounds, compositions and method of treating allergies |
CA2008878C (en) * | 1989-02-28 | 2003-01-21 | Michelangelo Scalone | Process for preparing pyridine-2-carboxamides |
US5672750A (en) * | 1994-12-16 | 1997-09-30 | Eastman Chemical Company | Preparation of aromatic amides from carbon monoxide, an amine and an aromatic chloride |
IL117798A (en) * | 1995-04-07 | 2001-11-25 | Schering Plough Corp | Tricyclic compounds useful for inhibition of g-protein function and for treatment of proliferative diseases and pharmaceutical compositions comprising them |
AR005152A1 (en) | 1995-12-22 | 1999-04-14 | Schering Corp | TRICYCLIC AMIDES USEFUL FOR THE INHIBITION OF THE FUNCTION OF PROTEIN-G, ITS SALTS, A PHARMACEUTICAL COMPOSITION THAT CONTAINS THEM AND THE USE OF THE SAME FOR THE MANUFACTURE OF A MEDICINAL PRODUCT FOR THE TREATMENT OF PROLIFERATIVE DISEASES |
SI0806415T1 (en) * | 1996-05-09 | 2000-04-30 | Lonza Ag | Process for the preparation of arylamides of heteroaromatic carboxylic acids |
US5958890A (en) * | 1996-09-13 | 1999-09-28 | Schering Corporation | Tricyclic compounds useful for inhibition of G-protein function and for treatment of proliferative diseases |
EP0977739B1 (en) * | 1997-03-25 | 2003-10-29 | Schering Corporation | Synthesis of intermediates useful in preparing tricyclic compounds |
-
1999
- 1999-11-18 AR ARP990105868A patent/AR028138A1/en active IP Right Grant
- 1999-11-18 TW TW088120161A patent/TW509680B/en not_active IP Right Cessation
- 1999-11-18 EP EP99972525A patent/EP1131296A2/en not_active Withdrawn
- 1999-11-18 AU AU37902/00A patent/AU3790200A/en not_active Abandoned
- 1999-11-18 CN CNB998135151A patent/CN1162404C/en not_active Expired - Lifetime
- 1999-11-18 WO PCT/US1999/026010 patent/WO2000030589A2/en active Application Filing
- 1999-11-18 JP JP2000583474A patent/JP4663122B2/en not_active Expired - Lifetime
- 1999-11-18 CO CO99072692A patent/CO5150169A1/en unknown
- 1999-11-18 CA CA002351693A patent/CA2351693C/en not_active Expired - Lifetime
- 1999-11-19 PE PE1999001170A patent/PE20001243A1/en not_active Application Discontinuation
- 1999-11-19 MY MYPI99005048A patent/MY121795A/en unknown
-
2001
- 2001-04-20 ZA ZA200103246A patent/ZA200103246B/en unknown
-
2002
- 2002-01-14 HK HK02100248.8A patent/HK1038698A1/en unknown
-
2010
- 2010-03-01 JP JP2010044749A patent/JP2010132701A/en not_active Withdrawn
Also Published As
Publication number | Publication date |
---|---|
CA2351693A1 (en) | 2000-06-02 |
CN1326444A (en) | 2001-12-12 |
CO5150169A1 (en) | 2002-04-29 |
HK1038698A1 (en) | 2002-03-28 |
TW509680B (en) | 2002-11-11 |
PE20001243A1 (en) | 2000-11-15 |
JP4663122B2 (en) | 2011-03-30 |
AU3790200A (en) | 2000-06-13 |
AR028138A1 (en) | 2003-04-30 |
WO2000030589A2 (en) | 2000-06-02 |
JP2010132701A (en) | 2010-06-17 |
CN1162404C (en) | 2004-08-18 |
WO2000030589A3 (en) | 2001-01-04 |
JP2002530307A (en) | 2002-09-17 |
CA2351693C (en) | 2009-01-20 |
EP1131296A2 (en) | 2001-09-12 |
ZA200103246B (en) | 2002-07-22 |
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