AR012661A1 - PROCESO PARA LA OBTENCIoN DE SERTINDOL: 1-[2-[4-[5-CLORO-1(4-FLUORFENIL)-1H-INDOL-3-IL]-1-PIPERIDINIL]ETIL]-2-IMIDAZOLIDINONA Y PROCESOS PARA PREPARAR INTERMEDIARIOS. - Google Patents
PROCESO PARA LA OBTENCIoN DE SERTINDOL: 1-[2-[4-[5-CLORO-1(4-FLUORFENIL)-1H-INDOL-3-IL]-1-PIPERIDINIL]ETIL]-2-IMIDAZOLIDINONA Y PROCESOS PARA PREPARAR INTERMEDIARIOS.Info
- Publication number
- AR012661A1 AR012661A1 ARP980102090A AR012661A1 AR 012661 A1 AR012661 A1 AR 012661A1 AR P980102090 A ARP980102090 A AR P980102090A AR 012661 A1 AR012661 A1 AR 012661A1
- Authority
- AR
- Argentina
- Prior art keywords
- chloro
- indole
- imidazolidinone
- sertindole
- fluorophenyl
- Prior art date
Links
- 238000000034 method Methods 0.000 title abstract 5
- GZKLJWGUPQBVJQ-UHFFFAOYSA-N sertindole Chemical compound C1=CC(F)=CC=C1N1C2=CC=C(Cl)C=C2C(C2CCN(CCN3C(NCC3)=O)CC2)=C1 GZKLJWGUPQBVJQ-UHFFFAOYSA-N 0.000 title abstract 4
- -1 4-fluorphenyl Chemical group 0.000 abstract 5
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 abstract 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract 3
- 229960000652 sertindole Drugs 0.000 abstract 3
- YGSFFDHIYYOVHV-UHFFFAOYSA-N 1-(2-chloroethyl)imidazolidin-2-one Chemical compound ClCCN1CCNC1=O YGSFFDHIYYOVHV-UHFFFAOYSA-N 0.000 abstract 2
- VRJHQPZVIGNGMX-UHFFFAOYSA-N 4-piperidinone Chemical compound O=C1CCNCC1 VRJHQPZVIGNGMX-UHFFFAOYSA-N 0.000 abstract 2
- 239000004471 Glycine Substances 0.000 abstract 2
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 abstract 2
- JBOPQACSHPPKEP-UHFFFAOYSA-N Indoxyl acetate Chemical compound C1=CC=C2C(OC(=O)C)=CNC2=C1 JBOPQACSHPPKEP-UHFFFAOYSA-N 0.000 abstract 2
- 229910052783 alkali metal Inorganic materials 0.000 abstract 2
- ZFIMCCCQJDZLCT-UHFFFAOYSA-N 2-(4-fluoroanilino)acetic acid Chemical compound OC(=O)CNC1=CC=C(F)C=C1 ZFIMCCCQJDZLCT-UHFFFAOYSA-N 0.000 abstract 1
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 abstract 1
- WLQZFXJVVNNEJU-UHFFFAOYSA-N 5-chloro-1-(4-fluorophenyl)-3-(1,2,3,6-tetrahydropyridin-4-yl)indole Chemical compound C1=CC(F)=CC=C1N1C2=CC=C(Cl)C=C2C(C=2CCNCC=2)=C1 WLQZFXJVVNNEJU-UHFFFAOYSA-N 0.000 abstract 1
- JYEKQDWSLSXYTJ-UHFFFAOYSA-N 5-chloro-1-(4-fluorophenyl)indole Chemical compound C1=CC(F)=CC=C1N1C2=CC=C(Cl)C=C2C=C1 JYEKQDWSLSXYTJ-UHFFFAOYSA-N 0.000 abstract 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 230000000561 anti-psychotic effect Effects 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 239000003153 chemical reaction reagent Substances 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 229910052802 copper Inorganic materials 0.000 abstract 1
- 239000010949 copper Substances 0.000 abstract 1
- 230000001351 cycling effect Effects 0.000 abstract 1
- 229940079593 drug Drugs 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 abstract 1
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
Landscapes
- Indole Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DK53697 | 1997-05-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR012661A1 true AR012661A1 (es) | 2000-11-08 |
Family
ID=8094655
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP980102090 AR012661A1 (es) | 1997-05-09 | 1998-05-05 | PROCESO PARA LA OBTENCIoN DE SERTINDOL: 1-[2-[4-[5-CLORO-1(4-FLUORFENIL)-1H-INDOL-3-IL]-1-PIPERIDINIL]ETIL]-2-IMIDAZOLIDINONA Y PROCESOS PARA PREPARAR INTERMEDIARIOS. |
Country Status (13)
-
1998
- 1998-04-27 MY MYPI9801885 patent/MY124162A/en unknown
- 1998-05-01 IN IN948MA1998 patent/IN187834B/en unknown
- 1998-05-04 ZA ZA983726A patent/ZA983726B/xx unknown
- 1998-05-04 CO CO98024289A patent/CO4950521A1/es unknown
- 1998-05-05 AR ARP980102090 patent/AR012661A1/es active IP Right Grant
- 1998-05-05 DZ DZ980094A patent/DZ2483A1/xx active
- 1998-05-07 CA CA002486883A patent/CA2486883C/en not_active Expired - Fee Related
- 1998-05-07 JO JO19982015A patent/JO2015B1/en active
- 1998-05-07 IL IL15618098A patent/IL156180A0/xx not_active IP Right Cessation
- 1998-05-08 PE PE00035498A patent/PE73199A1/es not_active Application Discontinuation
- 1998-05-08 TN TNTNSN98063A patent/TNSN98063A1/fr unknown
- 1998-05-11 MA MA25070A patent/MA25584A1/fr unknown
- 1998-07-02 TW TW87110712A patent/TW487692B/zh not_active IP Right Cessation
-
2000
- 2000-09-08 IN IN777MA2000 patent/IN190902B/en unknown
- 2000-09-18 IN IN776MA2000 patent/IN192270B/en unknown
Also Published As
Publication number | Publication date |
---|---|
JO2015B1 (en) | 1999-05-15 |
TNSN98063A1 (fr) | 2005-03-15 |
TW487692B (en) | 2002-05-21 |
IN190902B (enrdf_load_stackoverflow) | 2003-08-30 |
CA2486883C (en) | 2009-04-28 |
IN192270B (enrdf_load_stackoverflow) | 2004-03-27 |
PE73199A1 (es) | 1999-08-09 |
IN187834B (enrdf_load_stackoverflow) | 2002-06-29 |
MA25584A1 (fr) | 2002-12-31 |
DZ2483A1 (fr) | 2004-09-05 |
IL156180A0 (en) | 2003-12-23 |
CO4950521A1 (es) | 2000-09-01 |
ZA983726B (en) | 1998-11-24 |
CA2486883A1 (en) | 1998-11-19 |
MY124162A (en) | 2006-06-30 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
IS2324B (is) | Aðferð til framleiðslu á 5-klór-1-(flúorfenýl)-3-(1,2,3,6-tetrahydrópýridín-4-ýl) indól og aðferð til framleiðslu á sertindóli | |
RU2010144823A (ru) | Гетероциклические ингибиторы мек и способы их применения | |
EP1457487A4 (en) | PROCESS FOR PREPARING OPTICALLY ACTIVE CIS-PIPERIDINE DERIVATIVES | |
AR012661A1 (es) | PROCESO PARA LA OBTENCIoN DE SERTINDOL: 1-[2-[4-[5-CLORO-1(4-FLUORFENIL)-1H-INDOL-3-IL]-1-PIPERIDINIL]ETIL]-2-IMIDAZOLIDINONA Y PROCESOS PARA PREPARAR INTERMEDIARIOS. | |
NO995924L (no) | Fremgangsmåte ved fremstillingen av 1,4,7,10- tetraazacyklododekan-1,4,7-trieddiksyre og derivater derav | |
RU97120751A (ru) | Способ получения моногидрата ропивакаина гидрохлорида и моногидрат ропивакаина гидрохлорида, полученный этим способом | |
RU2003128651A (ru) | Способ получения 3-метилтиопропаналя | |
RU2002112756A (ru) | Способ получения N-(4,5-бис-метансульфонил-2-метилбензоил)гуанидина, гидрохлорида | |
CA2388915A1 (en) | Process for the preparation of n-(4,5-bismethanesulfonyl-2-methyl-benzoyl)guanidine, hydrochloride | |
JP2003261506A5 (enrdf_load_stackoverflow) | ||
WO2003031636A1 (fr) | Procede de production de 3-hydroxy-pentanenitrile optiquement actif | |
JP2005511779A5 (enrdf_load_stackoverflow) | ||
ATE349545T1 (de) | Enzymatisches verfahren zur herstellung von substituierter 2-amino-3-(2-amino-phenylsulfanyl)-propionsäure | |
NO20011031D0 (no) | FremgangsmÕte for fremstilling av N-beskyttede azetidin-2- karboksylsyrer (AzeOHs) | |
RU2003100063A (ru) | Способ получения n-метиланилина | |
RU97112575A (ru) | Способ получения 3-метакрилоксисульфолана | |
ATE420064T1 (de) | Unkatalysierte additionsreaktionen | |
RU2002112232A (ru) | Способ получения 7-амино-3-метоксиметил-3-цефем-4-карбоновой кислоты | |
DE50206142D1 (de) | Verfahren zur herstellung von 1,3-disubstituierten 2-nitroguanidinen | |
TH38719A (th) | กรรมวิธีสำหรับเตรียมไอโซโพรพิล-เมธิล-[2-(3-n-โพรพอกซิเฟนอกซิ)เอธิล]แอมีน | |
JP2003171367A5 (enrdf_load_stackoverflow) | ||
TH43464A3 (th) | ตัวกระทำเพื่อการเชื่อมประสานที่ได้รับการทำให้สิ้นสุดด้วยแอลกอฮอล์ | |
SE8403717L (sv) | Forfarande for framstellning av basiska tioetrar och salter derav |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FG | Grant; registration |