SI1233954T1 - A process for the preparation of 2- 4-(alpha-phenyl-p-chlorobenzyl)piperazin-1-yl)ethoxy acetic acid and novel intermediates therefor - Google Patents
A process for the preparation of 2- 4-(alpha-phenyl-p-chlorobenzyl)piperazin-1-yl)ethoxy acetic acid and novel intermediates thereforInfo
- Publication number
- SI1233954T1 SI1233954T1 SI200030569T SI200030569T SI1233954T1 SI 1233954 T1 SI1233954 T1 SI 1233954T1 SI 200030569 T SI200030569 T SI 200030569T SI 200030569 T SI200030569 T SI 200030569T SI 1233954 T1 SI1233954 T1 SI 1233954T1
- Authority
- SI
- Slovenia
- Prior art keywords
- phenyl
- chlorobenzyl
- piperazin
- alpha
- preparation
- Prior art date
Links
- YZGQDNOIGFBYKF-UHFFFAOYSA-N Ethoxyacetic acid Chemical compound CCOCC(O)=O YZGQDNOIGFBYKF-UHFFFAOYSA-N 0.000 title 2
- 239000000543 intermediate Substances 0.000 title 1
- -1 N,N-disubstituted {2-[-(alpha-phenyl-p-chlorobenzyl)piperazin-1-yl]ethoxy}acetamide Chemical class 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 125000001424 substituent group Chemical group 0.000 abstract 2
- FCTNBBLCKLLKIN-UHFFFAOYSA-N 2-[2-[2-[(4-chlorophenyl)-phenylmethyl]piperazin-1-yl]ethoxy]acetic acid Chemical compound OC(=O)COCCN1CCNCC1C(C=1C=CC(Cl)=CC=1)C1=CC=CC=C1 FCTNBBLCKLLKIN-UHFFFAOYSA-N 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 abstract 1
- 230000003301 hydrolyzing effect Effects 0.000 abstract 1
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/08—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms
- C07D295/084—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms with the ring nitrogen atoms and the oxygen or sulfur atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
- C07D295/088—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms with the ring nitrogen atoms and the oxygen or sulfur atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings to an acyclic saturated chain
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
HU9904439A HU226639B1 (en) | 1999-11-30 | 1999-11-30 | {2-[4-(alpha-phenyl-p-chloro-benzyl)-piperazine-1-yl]-ethoxy}-acetic acid-amides and process for producing them |
HU9904438A HU226641B1 (en) | 1999-11-30 | 1999-11-30 | Process for producing {2-[4-(alpha-phenyl-p-chloro-benzyl)-piperazine-1-yl]-ethoxy}-acetic acid |
PCT/HU2000/000123 WO2001040211A1 (en) | 1999-11-30 | 2000-11-29 | A PROCESS FOR THE PREPARATION OF {2-[4-(α-PHENYL-p-CHLOROBENZYL)PIPERAZIN-1-YL]ETHOXY}ACETIC ACID AND NOVEL INTERMEDIATES THEREFOR |
Publications (1)
Publication Number | Publication Date |
---|---|
SI1233954T1 true SI1233954T1 (en) | 2005-02-28 |
Family
ID=90000077
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SI200030569T SI1233954T1 (en) | 1999-11-30 | 2000-11-29 | A process for the preparation of 2- 4-(alpha-phenyl-p-chlorobenzyl)piperazin-1-yl)ethoxy acetic acid and novel intermediates therefor |
Country Status (15)
Country | Link |
---|---|
US (1) | US6908999B2 (cs) |
EP (1) | EP1233954B1 (cs) |
JP (1) | JP4763954B2 (cs) |
AT (1) | ATE280165T1 (cs) |
AU (1) | AU1874201A (cs) |
BG (1) | BG65455B1 (cs) |
CZ (1) | CZ304892B6 (cs) |
DE (1) | DE60015177T2 (cs) |
HR (1) | HRP20020470B1 (cs) |
PL (1) | PL200046B1 (cs) |
RU (1) | RU2248974C2 (cs) |
SI (1) | SI1233954T1 (cs) |
SK (1) | SK285641B6 (cs) |
UA (1) | UA72949C2 (cs) |
WO (1) | WO2001040211A1 (cs) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2454564A1 (en) * | 2001-07-26 | 2003-02-06 | Ucb, S.A. | Process for the preparation of 2-(2-(4-(bis(4-fluorophenyl)methyl)-piperazin-1-yl)ethoxy)acetic acid derivatives or corresponding salt forms thereof and intermediates therefor |
AU2003238883A1 (en) * | 2002-06-05 | 2003-12-22 | Dr.Reddy's Laboratories Ltd. | A novel amorphous form of (2-(4-((4-chlorophenyl)-phenyl methyl)-1- piperazinyl) ethoxy) acetic acid dihydrochloride (cetirizine dihydrochloride) |
HU227319B1 (en) * | 2005-12-08 | 2011-03-28 | Egis Gyogyszergyar Nyrt | Process for the production of (2-chloro-ethoxy)-acetic acid-n,n-dimethylamide and its intermediate and the novel intermediate |
HU227325B1 (en) * | 2005-12-08 | 2011-03-28 | Egis Gyogyszergyar Nyrt | Process for the production of an intermediate of (dextro- and levo)- cetirizine |
KR102034448B1 (ko) | 2017-12-20 | 2019-10-18 | 주식회사 포스코 | 강재 및 이의 제조 방법 |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NO155805C (no) | 1981-02-06 | 1987-06-10 | Ucb Sa | Analogifremgangsmaate for fremstilling av terapeutisk virksomme 2-(4-(difenylmethyl)-1-piperazinyl)-eddiksyrer og deres amider og ikke-toksiske salter. |
UA8337A1 (uk) * | 1981-02-06 | 1996-03-29 | Бальтес Ежен | 2-[4-(дифенілметіл)-1-піперазиніл]-оцтові кислоти або їх аміди, або їх нетоксичні фармацевтично прийняті солі, що проявляють спазмолітичну і антигістамінну активність |
US5347060A (en) * | 1991-07-24 | 1994-09-13 | Mobil Oil Corporation | Phase-transfer catalysis with onium-containing synthetic mesoporous crystalline material |
GB9305282D0 (en) * | 1993-03-15 | 1993-05-05 | Ucb Sa | Enantiomers of 1-(4-chlorophenyl)phenylmethyl)-4-(4-methylphenyl)sulphonyl)piperazine |
BE1010094A3 (fr) | 1996-04-10 | 1997-12-02 | Ucb Sa | Nouveaux [2-(1-piperazinyl)ethoxy] methyle substitues. |
CA2180993A1 (en) * | 1996-07-11 | 1998-01-12 | Yong Tao | Methods for the manufacture of cetirizine |
-
2000
- 2000-11-29 JP JP2001541895A patent/JP4763954B2/ja not_active Expired - Fee Related
- 2000-11-29 DE DE60015177T patent/DE60015177T2/de not_active Expired - Lifetime
- 2000-11-29 AU AU18742/01A patent/AU1874201A/en not_active Abandoned
- 2000-11-29 RU RU2002118101/04A patent/RU2248974C2/ru not_active IP Right Cessation
- 2000-11-29 US US10/148,704 patent/US6908999B2/en not_active Expired - Fee Related
- 2000-11-29 CZ CZ2002-1712A patent/CZ304892B6/cs not_active IP Right Cessation
- 2000-11-29 WO PCT/HU2000/000123 patent/WO2001040211A1/en active IP Right Grant
- 2000-11-29 SI SI200030569T patent/SI1233954T1/xx unknown
- 2000-11-29 UA UA2002065341A patent/UA72949C2/uk unknown
- 2000-11-29 AT AT00981508T patent/ATE280165T1/de not_active IP Right Cessation
- 2000-11-29 PL PL354677A patent/PL200046B1/pl unknown
- 2000-11-29 SK SK752-2002A patent/SK285641B6/sk not_active IP Right Cessation
- 2000-11-29 EP EP00981508A patent/EP1233954B1/en not_active Expired - Lifetime
-
2002
- 2002-05-28 HR HR20020470A patent/HRP20020470B1/xx not_active IP Right Cessation
- 2002-05-30 BG BG106760A patent/BG65455B1/bg unknown
Also Published As
Publication number | Publication date |
---|---|
US6908999B2 (en) | 2005-06-21 |
JP4763954B2 (ja) | 2011-08-31 |
DE60015177T2 (de) | 2005-10-27 |
PL200046B1 (pl) | 2008-11-28 |
AU1874201A (en) | 2001-06-12 |
SK285641B6 (sk) | 2007-05-03 |
DE60015177D1 (de) | 2004-11-25 |
CZ304892B6 (cs) | 2015-01-07 |
HRP20020470A2 (en) | 2004-04-30 |
RU2248974C2 (ru) | 2005-03-27 |
SK7522002A3 (en) | 2002-11-06 |
HRP20020470B1 (en) | 2009-04-30 |
UA72949C2 (uk) | 2005-05-16 |
BG65455B1 (bg) | 2008-08-29 |
BG106760A (en) | 2003-04-30 |
PL354677A1 (en) | 2004-02-09 |
ATE280165T1 (de) | 2004-11-15 |
JP2003515600A (ja) | 2003-05-07 |
WO2001040211A1 (en) | 2001-06-07 |
EP1233954A1 (en) | 2002-08-28 |
US20030092911A1 (en) | 2003-05-15 |
EP1233954B1 (en) | 2004-10-20 |
CZ20021712A3 (cs) | 2002-09-11 |
RU2002118101A (ru) | 2004-01-20 |
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