SK287067B6 - Spôsob syntézy esterov N-[(S)-1-karboxybutyl]-(S)-alanínu a ich použitie pri syntéze perindoprilu - Google Patents

Spôsob syntézy esterov N-[(S)-1-karboxybutyl]-(S)-alanínu a ich použitie pri syntéze perindoprilu Download PDF

Info

Publication number: SK287067B6
Authority: SK; Slovakia
Prior art keywords: formula; compound; synthesis; perindopril; iii
Prior art date: 2000-04-11

Application number

SK1457-2002A

Other languages

English (en)

Slovak (sk)

Other versions

SK14572002A3 (sk

Inventor

Jean-Claude Souvie

Alain Renaud

Original Assignee

Les Laboratoires Servier

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.)

2000-04-11

Filing date

2001-04-10

Publication date

2009-11-05

2001-04-10 Application filed by Les Laboratoires Servier filed Critical Les Laboratoires Servier

2003-02-04 Publication of SK14572002A3 publication Critical patent/SK14572002A3/sk

2009-11-05 Publication of SK287067B6 publication Critical patent/SK287067B6/sk

Links

230000015572 biosynthetic process Effects 0.000 title claims abstract description 20
238000000034 method Methods 0.000 title claims abstract description 20
238000003786 synthesis reaction Methods 0.000 title claims abstract description 19
IPVQLZZIHOAWMC-QXKUPLGCSA-N perindopril Chemical compound C1CCC[C@H]2C[C@@H](C(O)=O)N(C(=O)[C@H](C)N[C@@H](CCC)C(=O)OCC)[C@H]21 IPVQLZZIHOAWMC-QXKUPLGCSA-N 0.000 title claims description 8
229960002582 perindopril Drugs 0.000 title claims description 8
AMDDRMIFTJHJGD-WDSKDSINSA-N (2s)-2-[[(1s)-1-carboxyethyl]amino]pentanoic acid Chemical class CCC[C@@H](C(O)=O)N[C@@H](C)C(O)=O AMDDRMIFTJHJGD-WDSKDSINSA-N 0.000 title 1
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims abstract description 24
150000001875 compounds Chemical class 0.000 claims abstract description 22
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims abstract description 15
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 9
KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims abstract description 7
238000001914 filtration Methods 0.000 claims abstract description 6
238000005984 hydrogenation reaction Methods 0.000 claims abstract description 6
239000002244 precipitate Substances 0.000 claims abstract description 3
150000003839 salts Chemical class 0.000 claims description 7
QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 claims description 5
235000004279 alanine Nutrition 0.000 claims description 5
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 5
125000000217 alkyl group Chemical group 0.000 claims description 2
229910052799 carbon Inorganic materials 0.000 claims description 2
239000011541 reaction mixture Substances 0.000 abstract description 7
QNAYBMKLOCPYGJ-UHFFFAOYSA-N Alanine Chemical compound CC([NH3+])C([O-])=O QNAYBMKLOCPYGJ-UHFFFAOYSA-N 0.000 abstract description 3
230000020477 pH reduction Effects 0.000 abstract description 3
238000001953 recrystallisation Methods 0.000 abstract description 3
125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 1
230000000707 stereoselective effect Effects 0.000 abstract 1
238000002360 preparation method Methods 0.000 description 7
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 6
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 5
229960003767 alanine Drugs 0.000 description 5
238000006243 chemical reaction Methods 0.000 description 5
238000002955 isolation Methods 0.000 description 5
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
LCTONWCANYUPML-UHFFFAOYSA-N Pyruvic acid Chemical compound CC(=O)C(O)=O LCTONWCANYUPML-UHFFFAOYSA-N 0.000 description 4
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
239000011780 sodium chloride Substances 0.000 description 3
101800000734 Angiotensin-1 Proteins 0.000 description 2
102400000344 Angiotensin-1 Human genes 0.000 description 2
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
ORWYRWWVDCYOMK-HBZPZAIKSA-N angiotensin I Chemical compound C([C@@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CC=1NC=NC=1)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)N[C@@H](CC=1NC=NC=1)C(=O)N[C@@H](CC(C)C)C(O)=O)NC(=O)[C@@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H](N)CC(O)=O)C(C)C)C1=CC=C(O)C=C1 ORWYRWWVDCYOMK-HBZPZAIKSA-N 0.000 description 2
DPBOUPADTRCCIH-UHFFFAOYSA-N ethyl 2-aminopentanoate Chemical compound CCCC(N)C(=O)OCC DPBOUPADTRCCIH-UHFFFAOYSA-N 0.000 description 2
YERWBBMSDMSDKT-UHFFFAOYSA-N ethyl 2-oxopentanoate Chemical compound CCCC(=O)C(=O)OCC YERWBBMSDMSDKT-UHFFFAOYSA-N 0.000 description 2
238000001704 evaporation Methods 0.000 description 2
230000008020 evaporation Effects 0.000 description 2
229910052739 hydrogen Inorganic materials 0.000 description 2
239000001257 hydrogen Substances 0.000 description 2
229940107700 pyruvic acid Drugs 0.000 description 2
102000005862 Angiotensin II Human genes 0.000 description 1
101800000733 Angiotensin-2 Proteins 0.000 description 1
101800004538 Bradykinin Proteins 0.000 description 1
102400000967 Bradykinin Human genes 0.000 description 1
208000024172 Cardiovascular disease Diseases 0.000 description 1
102000004190 Enzymes Human genes 0.000 description 1
108090000790 Enzymes Proteins 0.000 description 1
QXZGBUJJYSLZLT-UHFFFAOYSA-N H-Arg-Pro-Pro-Gly-Phe-Ser-Pro-Phe-Arg-OH Natural products NC(N)=NCCCC(N)C(=O)N1CCCC1C(=O)N1C(C(=O)NCC(=O)NC(CC=2C=CC=CC=2)C(=O)NC(CO)C(=O)N2C(CCC2)C(=O)NC(CC=2C=CC=CC=2)C(=O)NC(CCCN=C(N)N)C(O)=O)CCC1 QXZGBUJJYSLZLT-UHFFFAOYSA-N 0.000 description 1
206010019280 Heart failures Diseases 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
CZGUSIXMZVURDU-JZXHSEFVSA-N Ile(5)-angiotensin II Chemical compound C([C@@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CC=1NC=NC=1)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](CC=1C=CC=CC=1)C([O-])=O)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(N)=[NH2+])NC(=O)[C@@H]([NH3+])CC([O-])=O)C(C)C)C1=CC=C(O)C=C1 CZGUSIXMZVURDU-JZXHSEFVSA-N 0.000 description 1
QNAYBMKLOCPYGJ-UWTATZPHSA-N L-Alanine Natural products C[C@@H](N)C(O)=O QNAYBMKLOCPYGJ-UWTATZPHSA-N 0.000 description 1
102000004270 Peptidyl-Dipeptidase A Human genes 0.000 description 1
108090000882 Peptidyl-Dipeptidase A Proteins 0.000 description 1
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
229950006323 angiotensin ii Drugs 0.000 description 1
208000037849 arterial hypertension Diseases 0.000 description 1
230000009286 beneficial effect Effects 0.000 description 1
YGYLYUIRSJSFJS-QMMMGPOBSA-N benzyl (2s)-2-aminopropanoate Chemical compound C[C@H](N)C(=O)OCC1=CC=CC=C1 YGYLYUIRSJSFJS-QMMMGPOBSA-N 0.000 description 1
QXZGBUJJYSLZLT-FDISYFBBSA-N bradykinin Chemical compound NC(=N)NCCC[C@H](N)C(=O)N1CCC[C@H]1C(=O)N1[C@H](C(=O)NCC(=O)N[C@@H](CC=2C=CC=CC=2)C(=O)N[C@@H](CO)C(=O)N2[C@@H](CCC2)C(=O)N[C@@H](CC=2C=CC=CC=2)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O)CCC1 QXZGBUJJYSLZLT-FDISYFBBSA-N 0.000 description 1
230000015556 catabolic process Effects 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
239000003638 chemical reducing agent Substances 0.000 description 1
239000012043 crude product Substances 0.000 description 1
238000002425 crystallisation Methods 0.000 description 1
230000008025 crystallization Effects 0.000 description 1
238000006731 degradation reaction Methods 0.000 description 1
239000012065 filter cake Substances 0.000 description 1
239000000706 filtrate Substances 0.000 description 1
150000002431 hydrogen Chemical class 0.000 description 1
239000012535 impurity Substances 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
239000011976 maleic acid Substances 0.000 description 1
239000011707 mineral Substances 0.000 description 1
150000007522 mineralic acids Chemical class 0.000 description 1
239000000203 mixture Substances 0.000 description 1
239000005445 natural material Substances 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
229910052763 palladium Inorganic materials 0.000 description 1
230000000144 pharmacologic effect Effects 0.000 description 1
230000002265 prevention Effects 0.000 description 1
108090000765 processed proteins & peptides Proteins 0.000 description 1
238000000746 purification Methods 0.000 description 1
BEOOHQFXGBMRKU-UHFFFAOYSA-N sodium cyanoborohydride Chemical compound [Na+].[B-]C#N BEOOHQFXGBMRKU-UHFFFAOYSA-N 0.000 description 1
239000007787 solid Substances 0.000 description 1
230000001225 therapeutic effect Effects 0.000 description 1
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
239000005526 vasoconstrictor agent Substances 0.000 description 1
229940124549 vasodilator Drugs 0.000 description 1
239000003071 vasodilator agent Substances 0.000 description 1
231100000925 very toxic Toxicity 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C227/00—Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton
- C07C227/30—Preparation of optical isomers
- C07C227/32—Preparation of optical isomers by stereospecific synthesis
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/07—Optical isomers

Landscapes

Organic Chemistry (AREA)
Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Bioinformatics & Cheminformatics (AREA)
Engineering & Computer Science (AREA)
Medicinal Chemistry (AREA)
Veterinary Medicine (AREA)
Life Sciences & Earth Sciences (AREA)
Pharmacology & Pharmacy (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Chemical Kinetics & Catalysis (AREA)
Cardiology (AREA)
General Chemical & Material Sciences (AREA)
Animal Behavior & Ethology (AREA)
General Health & Medical Sciences (AREA)
Public Health (AREA)
Heart & Thoracic Surgery (AREA)
Hospice & Palliative Care (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Peptides Or Proteins (AREA)
Indole Compounds (AREA)
Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

SK1457-2002A 2000-04-11 2001-04-10 Spôsob syntézy esterov N-[(S)-1-karboxybutyl]-(S)-alanínu a ich použitie pri syntéze perindoprilu SK287067B6 (sk)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
FR0004610A FR2807430B1 (fr)	2000-04-11	2000-04-11	Nouveau procede de synthese des esters de la n-[(s)-1- carboxybutyl]-(s)-alanine et application a la synthese du perindopril
PCT/FR2001/001088 WO2001056972A1 (fr)	2000-04-11	2001-04-10	Nouveau procede de synthese des esters de la n-[(s)-1-carboxybutyl]-(s)-alanine et application a la synthese du perindopril

Publications (2)

Publication Number	Publication Date
SK14572002A3 SK14572002A3 (sk)	2003-02-04
SK287067B6 true SK287067B6 (sk)	2009-11-05

Family

ID=8849107

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SK1457-2002A SK287067B6 (sk)	2000-04-11	2001-04-10	Spôsob syntézy esterov N-[(S)-1-karboxybutyl]-(S)-alanínu a ich použitie pri syntéze perindoprilu

Country Status (35)

Country	Link
US (1)	US6774259B2 (es)
EP (1)	EP1272454B1 (es)
JP (1)	JP3872344B2 (es)
KR (1)	KR100520700B1 (es)
CN (1)	CN1176903C (es)
AP (1)	AP1417A (es)
AR (1)	AR027782A1 (es)
AT (1)	ATE362913T1 (es)
AU (2)	AU5046701A (es)
BG (1)	BG65833B1 (es)
BR (1)	BR0109963A (es)
CA (1)	CA2405466C (es)
CY (1)	CY1106720T1 (es)
CZ (1)	CZ302603B6 (es)
DE (1)	DE60128554T2 (es)
DK (1)	DK1272454T3 (es)
EA (1)	EA004265B1 (es)
EE (1)	EE05030B1 (es)
ES (1)	ES2287114T3 (es)
FR (1)	FR2807430B1 (es)
GE (1)	GEP20063798B (es)
HR (1)	HRP20020887B1 (es)
HU (1)	HU229189B1 (es)
ME (1)	ME00442B (es)
MX (1)	MXPA02009888A (es)
NO (1)	NO327970B1 (es)
NZ (1)	NZ521846A (es)
OA (1)	OA12246A (es)
PL (1)	PL346553A1 (es)
PT (1)	PT1272454E (es)
RS (1)	RS50240B (es)
SK (1)	SK287067B6 (es)
UA (1)	UA72040C2 (es)
WO (1)	WO2001056972A1 (es)
ZA (1)	ZA200207689B (es)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR2807037B1 (fr) *	2000-03-31	2002-05-10	Adir	NOUVEAU PROCEDE DE SYNTHESE DES ESTERS DE LA N-[(s)-1- CARBOXYBUTYL]-(S)-ALANINE ET APPLICATION A LA SYNTHESE DU PERINDOPRIL
FR2827860B1 (fr)	2001-07-24	2004-12-10	Servier Lab	Nouveau procede de synthese de derives de l'acide (2s, 3as, 7as)-1-[(s)-alanyl]-octahydro-1h-indole-2-carboxyline et application a la synthese du perindopril
ATE395913T1 (de)	2003-02-28	2008-06-15	Servier S A Lab	Verfahren zur herstellung von perindopril
SI1362845T1 (sl) *	2003-09-01	2010-01-29	Servier Lab	Nov postopek za pripravo estrov n((s)-1-karboksibutil)-(s)-alanina in uporaba za sintezo perindoprila
EP1400531B1 (fr) *	2003-09-30	2006-01-04	Les Laboratoires Servier	Procédé de synthèse de la N-[(S)-1-carbéthoxybutyl]-(S)-alanine et application à la synthèse du perindopril
PT1403278E (pt) *	2003-09-30	2005-09-30	Servier Lab	Processo de sintese da n-((s)-1-carbetoxibutil)-(s)-alanina e aplicacao a sintese do perindopril
HRP20161602T1 (hr) *	2004-03-29	2016-12-30	Les Laboratoires Servier	Postupak priprave čvrstog farmaceutskog pripravka
SI21800A (sl)	2004-05-14	2005-12-31	Krka, Tovarna Zdravil, D.D., Novo Mesto	Nov postopek sinteze perindoprila
EP1792896A1 (en)	2005-12-01	2007-06-06	KRKA, tovarna zdravil, d.d., Novo mesto	Process for the preparation of perindopril and salts thereof
FI126564B (fi)	2011-02-28	2017-02-15	Andritz Oy	Menetelmä ja laitteisto meesan polttamiseksi
CN107098949B (zh) *	2017-04-20	2021-03-16	上药东英（江苏）药业有限公司	一种制备培哚普利叔丁胺盐的绿色合成新工艺

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR2503155A2 (fr) *	1980-10-02	1982-10-08	Science Union & Cie	Nouveaux imino diacides substitues, leurs procedes de preparation et leur emploi comme inhibiteur d'enzyme
US4344949A (en) *	1980-10-03	1982-08-17	Warner-Lambert Company	Substituted acyl derivatives of 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acids
US4296110A (en) *	1980-10-28	1981-10-20	E. I. Du Pont De Nemours And Company	Antihypertensive I-substituted cyclic lactam-2-carboxylic acids
US4503043A (en) *	1981-12-07	1985-03-05	Warner-Lambert Company	Substituted acyl derivatives of octahydro-1H-isoindole-1-carboxylic acids
FR2620700B1 (fr) *	1987-09-17	1990-06-01	Adir	Procede de synthese d'alpha amino acides n alkyles et leurs esters. application a la synthese de carboxyalkyl dipeptides
FR2620699B1 (fr) *	1987-09-17	1990-06-01	Adir	Procede de synthese d'alpha amino acides n alkyles et de leurs esters. application a la synthese de carboxyalkyl dipeptides
FR2620709B1 (fr) *	1987-09-17	1990-09-07	Adir	Procede de synthese industrielle du perindopril et de ses principaux intermediaires de synthese

2000
- 2000-04-11 FR FR0004610A patent/FR2807430B1/fr not_active Expired - Fee Related
2001
- 2001-03-20 PL PL01346553A patent/PL346553A1/xx not_active Application Discontinuation
- 2001-03-30 HU HU0101337A patent/HU229189B1/hu not_active IP Right Cessation
- 2001-04-09 AR ARP010101670A patent/AR027782A1/es not_active Application Discontinuation
- 2001-04-10 NZ NZ521846A patent/NZ521846A/en not_active IP Right Cessation
- 2001-04-10 AP APAP/P/2002/002639A patent/AP1417A/en active
- 2001-04-10 PT PT01923776T patent/PT1272454E/pt unknown
- 2001-04-10 KR KR10-2002-7013604A patent/KR100520700B1/ko not_active Expired - Fee Related
- 2001-04-10 AU AU5046701A patent/AU5046701A/xx active Pending
- 2001-04-10 US US10/257,239 patent/US6774259B2/en not_active Expired - Lifetime
- 2001-04-10 JP JP2001556822A patent/JP3872344B2/ja not_active Expired - Fee Related
- 2001-04-10 BR BR0109963-9A patent/BR0109963A/pt not_active Application Discontinuation
- 2001-04-10 ME MEP-2008-671A patent/ME00442B/me unknown
- 2001-04-10 RS YU76702A patent/RS50240B/sr unknown
- 2001-04-10 MX MXPA02009888A patent/MXPA02009888A/es active IP Right Grant
- 2001-04-10 CA CA002405466A patent/CA2405466C/fr not_active Expired - Fee Related
- 2001-04-10 HR HR20020887A patent/HRP20020887B1/xx not_active IP Right Cessation
- 2001-04-10 CN CNB018079210A patent/CN1176903C/zh not_active Expired - Fee Related
- 2001-04-10 ES ES01923776T patent/ES2287114T3/es not_active Expired - Lifetime
- 2001-04-10 OA OA1200200313A patent/OA12246A/en unknown
- 2001-04-10 SK SK1457-2002A patent/SK287067B6/sk not_active IP Right Cessation
- 2001-04-10 AT AT01923776T patent/ATE362913T1/de active
- 2001-04-10 DE DE60128554T patent/DE60128554T2/de not_active Expired - Lifetime
- 2001-04-10 GE GEAP20016688A patent/GEP20063798B/en unknown
- 2001-04-10 CZ CZ20023323A patent/CZ302603B6/cs not_active IP Right Cessation
- 2001-04-10 EP EP01923776A patent/EP1272454B1/fr not_active Expired - Lifetime
- 2001-04-10 WO PCT/FR2001/001088 patent/WO2001056972A1/fr not_active Ceased
- 2001-04-10 DK DK01923776T patent/DK1272454T3/da active
- 2001-04-10 EA EA200201049A patent/EA004265B1/ru not_active IP Right Cessation
- 2001-04-10 AU AU2001250467A patent/AU2001250467B2/en not_active Ceased
- 2001-04-10 EE EEP200200586A patent/EE05030B1/xx not_active IP Right Cessation
- 2001-10-04 UA UA2002118916A patent/UA72040C2/uk unknown
2002
- 2002-09-25 ZA ZA200207689A patent/ZA200207689B/xx unknown
- 2002-10-04 NO NO20024811A patent/NO327970B1/no not_active IP Right Cessation
- 2002-11-04 BG BG107250A patent/BG65833B1/bg unknown
2007
- 2007-07-12 CY CY20071100924T patent/CY1106720T1/el unknown

Also Published As

Publication number	Publication date
YU76702A (sh)	2006-05-25
GEP20063798B (en)	2006-04-25
CA2405466A1 (fr)	2001-08-09
EA200201049A1 (ru)	2003-02-27
CN1422245A (zh)	2003-06-04
HU229189B1 (hu)	2013-09-30
PL346553A1 (en)	2001-09-10
HRP20020887B1 (en)	2011-03-31
ZA200207689B (en)	2003-09-25
HK1053300A1 (en)	2003-10-17
CZ20023323A3 (cs)	2003-01-15
CA2405466C (fr)	2005-02-15
EE05030B1 (et)	2008-06-16
HRP20020887A2 (en)	2004-02-29
AR027782A1 (es)	2003-04-09
AU2001250467B2 (en)	2005-02-17
EP1272454B1 (fr)	2007-05-23
ME00442B (me)	2011-10-10
WO2001056972A1 (fr)	2001-08-09
SK14572002A3 (sk)	2003-02-04
JP3872344B2 (ja)	2007-01-24
BG65833B1 (bg)	2010-02-26
DE60128554D1 (de)	2007-07-05
KR20020093902A (ko)	2002-12-16
EA004265B1 (ru)	2004-02-26
CY1106720T1 (el)	2012-05-23
JP2003521530A (ja)	2003-07-15
AP1417A (en)	2005-05-24
EE200200586A (et)	2004-04-15
BR0109963A (pt)	2003-08-05
RS50240B (sr)	2009-07-15
CZ302603B6 (cs)	2011-08-03
DK1272454T3 (da)	2007-09-17
ES2287114T3 (es)	2007-12-16
US6774259B2 (en)	2004-08-10
CN1176903C (zh)	2004-11-24
ATE362913T1 (de)	2007-06-15
DE60128554T2 (de)	2008-02-21
AP2002002639A0 (en)	2002-09-30
PT1272454E (pt)	2007-08-01
KR100520700B1 (ko)	2005-10-17
OA12246A (en)	2003-12-08
FR2807430A1 (fr)	2001-10-12
FR2807430B1 (fr)	2002-05-17
NO20024811L (no)	2002-10-04
MXPA02009888A (es)	2004-09-06
UA72040C2 (en)	2005-01-17
NZ521846A (en)	2004-07-30
HUP0101337A3 (en)	2002-11-28
EP1272454A1 (fr)	2003-01-08
HU0101337D0 (en)	2001-06-28
AU5046701A (en)	2001-08-14
HUP0101337A2 (hu)	2001-11-28
NO20024811D0 (no)	2002-10-04
NO327970B1 (no)	2009-11-02
BG107250A (bg)	2003-06-30
US20030109743A1 (en)	2003-06-12

Publication	Publication Date	Title
SK286921B6 (sk)	2009-07-06	Spôsob syntézy perindoprilu a jeho farmaceuticky prijateľných solí
SK287067B6 (sk)	2009-11-05	Spôsob syntézy esterov N-[(S)-1-karboxybutyl]-(S)-alanínu a ich použitie pri syntéze perindoprilu
US6818788B2 (en)	2004-11-16	Method for synthesis of n-[(s)-1-carboxybutyl]-(s)-alanine esters and use in synthesis of perindopril
HK1053300B (en)	2005-04-01	Method for synthesis of n-[(s)-1-carboxybutyl]-(s)-alanine esters and use in synthesis of perindopril

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