DE60112305D1 - Verfahren zur herstellung amlodipinmaleat - Google Patents

Verfahren zur herstellung amlodipinmaleat

Info

Publication number
DE60112305D1
DE60112305D1 DE60112305T DE60112305T DE60112305D1 DE 60112305 D1 DE60112305 D1 DE 60112305D1 DE 60112305 T DE60112305 T DE 60112305T DE 60112305 T DE60112305 T DE 60112305T DE 60112305 D1 DE60112305 D1 DE 60112305D1
Authority
DE
Germany
Prior art keywords
amlodipinmaleat
preparing
preparing amlodipinmaleat
Prior art date
Legal status (The legal status 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 status listed.)
Revoked
Application number
DE60112305T
Other languages
English (en)
Other versions
DE60112305T2 (de
Inventor
Frantisek Picha
Pavel Slanina
Bernardus Benneker
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Pfizer Ltd
Original Assignee
Pfizer Ltd
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=29740325&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=DE60112305(D1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Pfizer Ltd filed Critical Pfizer Ltd
Application granted granted Critical
Publication of DE60112305D1 publication Critical patent/DE60112305D1/de
Publication of DE60112305T2 publication Critical patent/DE60112305T2/de
Anticipated expiration legal-status Critical
Revoked legal-status Critical Current

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4422—1,4-Dihydropyridines, e.g. nifedipine, nicardipine
    • 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
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • 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
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/80—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
    • C07D211/84—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members 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
    • C07D211/90—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
DE60112305T 2000-12-29 2001-08-15 Verfahren zur herstellung amlodipinmaleat Revoked DE60112305T2 (de)

Applications Claiming Priority (6)

Application Number Priority Date Filing Date Title
US25861200P 2000-12-29 2000-12-29
US258612P 2000-12-29
US80934301A 2001-03-16 2001-03-16
US809343 2001-03-16
PCT/NL2001/000607 WO2002053542A1 (en) 2000-12-29 2001-08-15 Process for making amlodipine maleate
BE2001/0709A BE1014452A6 (nl) 2000-12-29 2001-11-05 Werkwijze voor het maken van amlodipinemaleaat.

Publications (2)

Publication Number Publication Date
DE60112305D1 true DE60112305D1 (de) 2005-09-01
DE60112305T2 DE60112305T2 (de) 2006-05-24

Family

ID=29740325

Family Applications (2)

Application Number Title Priority Date Filing Date
DE60112305T Revoked DE60112305T2 (de) 2000-12-29 2001-08-15 Verfahren zur herstellung amlodipinmaleat
DE20115704U Ceased DE20115704U1 (de) 2000-12-29 2001-09-25 Amlodipinmaleat mit hoher Reinheit

Family Applications After (1)

Application Number Title Priority Date Filing Date
DE20115704U Ceased DE20115704U1 (de) 2000-12-29 2001-09-25 Amlodipinmaleat mit hoher Reinheit

Country Status (25)

Country Link
US (2) US6600047B2 (de)
EP (1) EP1309555B1 (de)
CN (1) CN1272319C (de)
AP (1) AP2003002820A0 (de)
AT (3) ATE300520T1 (de)
BE (1) BE1014452A6 (de)
BR (1) BR0116557A (de)
CA (1) CA2433288C (de)
DE (2) DE60112305T2 (de)
DK (3) DK1309555T3 (de)
ES (1) ES2243553T3 (de)
FI (1) FI6788U1 (de)
HK (2) HK1055965A1 (de)
HR (1) HRP20030526A2 (de)
IL (1) IL156692A0 (de)
IS (1) IS6834A (de)
MA (1) MA25984A1 (de)
MX (1) MXPA03005885A (de)
NO (1) NO20032518L (de)
NZ (1) NZ526506A (de)
PL (1) PL362660A1 (de)
PT (1) PT1309555E (de)
RS (1) RS53403A (de)
SI (1) SI1309555T1 (de)
WO (1) WO2002053542A1 (de)

Families Citing this family (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6653481B2 (en) * 2000-12-29 2003-11-25 Synthon Bv Process for making amlodipine
EP1309558A1 (de) * 2000-12-29 2003-05-14 Synthon Licensing, Ltd. Aspartat-derivat von amlodipine als kalzium-kanal antagonist
MXPA03005882A (es) * 2000-12-29 2005-04-19 Pfizer Ltd Derivado amida de amlodipina.
CA2433193C (en) * 2000-12-29 2006-01-31 Pfizer Limited Amide derivative of amlodipine
EP1309555B1 (de) 2000-12-29 2005-07-27 Pfizer Limited Verfahren zur herstellung amlodipinmaleat
US20030027848A1 (en) * 2001-06-15 2003-02-06 Anne Billotte Stabilized formulations
GB0114709D0 (en) * 2001-06-15 2001-08-08 Pfizer Ltd Stabilised formulations of amlodipine maleate
US20030180354A1 (en) * 2001-10-17 2003-09-25 Dr. Reddy's Laboratories Limited Amlodipine maleate formulations
KR100496436B1 (ko) 2002-07-30 2005-06-20 씨제이 주식회사 암로디핀의 유기산염
KR100538641B1 (ko) * 2002-07-30 2005-12-22 씨제이 주식회사 암로디핀의 유기산염
KR100467669B1 (ko) 2002-08-21 2005-01-24 씨제이 주식회사 암로디핀의 유기산염
AU2003253460A1 (en) * 2002-09-19 2004-04-08 Cj Corporation Crystalline organic acid salt of amlodipine
EP1407773A1 (de) * 2002-10-08 2004-04-14 Council of Scientific and Industrial Research Verfahren zur Herstellung von s(-)Amlodipin-Salzen
US20040072879A1 (en) * 2002-10-10 2004-04-15 Dr. Reddy's Laboratories Limited Crystalline 2-[(2-aminoethoxy)methyl]-4-(2-chlorophenyl)-3-ethoxycarbonyl-5-methoxycarbonyl-6-methyl-1,4-dihydropyridine maleate salt (Amlodipine)
WO2004058711A1 (en) * 2002-12-30 2004-07-15 Eos Eczacibasi Ozgun Kimyasal Urunler Sanayi Ve Ticaret A.S. Isolation of dihydropyridine derivative and preparation salts thereof
WO2005023769A1 (en) * 2003-09-04 2005-03-17 Cipla Limited Process for the preparation of amlodipine salts
BRPI0416648A2 (pt) * 2003-11-20 2009-01-13 Council Scient Ind Res processo para a preparaÇço de sais quirais farmaceuticamente aceitÁveis de amlodipina
US20060030602A1 (en) * 2004-03-16 2006-02-09 Sepracor Inc. (S)-amlodipine malate
PT2404906E (pt) * 2006-11-02 2015-11-02 Millennium Pharm Inc Métodos de sintetizar sais farmacêuticos de um inibidor de fator xa
KR100843400B1 (ko) * 2006-11-14 2008-07-04 씨제이제일제당 (주) 결정성 ｓ-(-)-암로디핀 말레익산 염 무수물 및 이의제조방법
US20090062352A1 (en) * 2007-08-29 2009-03-05 Protia, Llc Deuterium-enriched amlodipine
CN102344409B (zh) * 2011-07-20 2013-04-03 海南锦瑞制药股份有限公司 一种氨氯地平晶体、其与贝那普利药用组合物及制备方法
CN102382041B (zh) * 2011-12-02 2016-01-20 东北制药集团股份有限公司 一种马来酸氨氯地平的制备方法
CN103044314A (zh) * 2013-01-06 2013-04-17 先声药业有限公司 马来酸氨氯地平的制备方法
CN104529877A (zh) * 2015-01-22 2015-04-22 华东理工常熟研究院有限公司 氨氯地平-癸酸离子液体及其制备方法和用途
ES2886067T3 (es) 2016-10-07 2021-12-16 Silvergate Pharmaceuticals Inc Formulaciones de amlodipina
CN108358833A (zh) * 2018-03-15 2018-08-03 上海峰林生物科技有限公司 一种马来酸氨氯地平的合成工艺
US10799453B2 (en) 2018-04-11 2020-10-13 Silvergate Pharmaceuticals, Inc. Amlodipine formulations
CN109651236A (zh) * 2019-01-24 2019-04-19 浙江尖峰药业有限公司 门冬氨酸氨氯地平的晶型及其制备和应用

Family Cites Families (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4294969A (en) * 1979-01-29 1981-10-13 Merck & Co., Inc. Process for producing 2-bromo-3,5-disubstituted pyridines
CS228917B2 (en) * 1981-03-14 1984-05-14 Pfizer Method of preparing substituted derivatives of 1,4-dihydropyridine
DK161312C (da) 1982-03-11 1991-12-09 Pfizer Analogifremgangsmaade til fremstilling af 2-aminoalkoxymethyl-4-phenyl-6-methyl-1,4-dihydropyridin-3,5-dicarboxylsyreestere eller syreadditionssalte deraf samt phthalimidoderivater til anvendelse som udgangsmateriale ved fremgangsmaaden
GR851819B (de) * 1984-08-17 1985-11-26 Wyeth John & Brother Ltd
IT1201454B (it) * 1985-08-19 1989-02-02 Boehringer Biochemia Srl 1,4-diidropiridine-2-sostituite
GB8608335D0 (en) 1986-04-04 1986-05-08 Pfizer Ltd Pharmaceutically acceptable salts
FR2602231B1 (fr) * 1986-08-04 1988-10-28 Adir Nouveaux derives de la dihydro-1,4 pyridine, leurs procedes de preparation et les compositions pharmaceutiques qui les contiennent
US4983740A (en) 1986-08-04 1991-01-08 Adir Et Compagnie Process for 1,4-dihydropyridine compounds
GB8710493D0 (en) 1987-05-02 1987-06-03 Pfizer Ltd Dihydropyridines
US5155120A (en) 1991-01-14 1992-10-13 Pfizer Inc Method for treating congestive heart failure
WO1993006082A1 (en) 1991-09-13 1993-04-01 Merck & Co., Inc. Process for the preparation of 4-substituted-1,4-dihydropyridines
US5389654A (en) 1992-11-26 1995-02-14 Lek, Tovarna, Farmacevtskih In Kemicnih . . . 3-ethyl 5-methyl(±)2-[2-(N-tritylamino)ethoxymethyl]-4-(2-chlorophenyl)-1,4-dihydro-6-methyl-6-methyl-3,5-pyridinedicarboxylate
HU221810B1 (hu) 1997-08-12 2003-01-28 EGIS Gyógyszergyár Rt. Eljárás amlodipin-bezilát előállítására és az eljárás intermedierjei
ZA9810320B (en) 1997-11-14 2000-05-11 Gea Farmaceutisk Fabrik As Process for the preparation of 1,4-dihydropyridines and novel compounds of use for such purpose.
ZA9810319B (en) * 1997-11-14 2000-05-11 Gea Farmaceutisk Fabrik As Process for the preparation of acetal derivatives of 1,4-dihydropyridines, novel acetal derivatives and the use of the acetal derivatives for the preparation of other 1,4-dihydropyridines.
PL189666B1 (pl) * 1998-04-09 2005-09-30 Adamed Sp Z Oo Sposób otrzymywania benzenosulfonianu amlodypiny
GB9812413D0 (en) 1998-06-10 1998-08-05 Glaxo Group Ltd Compound and its use
ES2151850B1 (es) 1998-10-26 2001-08-16 Esteve Quimica Sa Intermedio para la sintesis de amlodipino para su obtencion y utilizacion correspondiente.
GB9827431D0 (en) 1998-12-11 1999-02-03 Smithkline Beecham Plc Novel compound
GB9827387D0 (en) 1998-12-11 1999-02-03 Smithkline Beecham Plc Novel process
CA2433193C (en) * 2000-12-29 2006-01-31 Pfizer Limited Amide derivative of amlodipine
CA2433181C (en) * 2000-12-29 2005-11-22 Pfizer Limited Amlodipine hemifumarate
EP1309558A1 (de) * 2000-12-29 2003-05-14 Synthon Licensing, Ltd. Aspartat-derivat von amlodipine als kalzium-kanal antagonist
WO2002053539A1 (en) * 2000-12-29 2002-07-11 Pfizer Limited Amlodipine hemimaleate
EP1309555B1 (de) * 2000-12-29 2005-07-27 Pfizer Limited Verfahren zur herstellung amlodipinmaleat

Also Published As

Publication number Publication date
FI6788U1 (fi) 2005-09-14
IS6834A (is) 2003-05-30
PT1309555E (pt) 2005-10-31
DK200300344U4 (da) 2005-09-09
BE1014452A6 (nl) 2003-10-07
CA2433288A1 (en) 2002-07-11
ES2243553T3 (es) 2005-12-01
HRP20030526A2 (en) 2005-06-30
DK200300345U3 (da) 2004-03-12
BR0116557A (pt) 2003-10-28
AT7110U2 (de) 2004-10-25
NO20032518L (no) 2003-06-26
DK200300344U1 (da) 2003-12-12
SI1309555T1 (sl) 2005-12-31
US6600047B2 (en) 2003-07-29
HK1055965A1 (en) 2004-01-30
NO20032518D0 (no) 2003-06-04
DK1309555T3 (da) 2005-10-24
MXPA03005885A (es) 2005-04-19
NZ526506A (en) 2004-11-26
US20020086888A1 (en) 2002-07-04
CA2433288C (en) 2006-06-13
EP1309555B1 (de) 2005-07-27
CN1505614A (zh) 2004-06-16
IL156692A0 (en) 2004-01-04
CN1272319C (zh) 2006-08-30
AT7109U3 (de) 2005-05-25
ATE300520T1 (de) 2005-08-15
DE60112305T2 (de) 2006-05-24
RS53403A (en) 2006-10-27
AT7110U9 (de) 2004-11-25
MA25984A1 (fr) 2003-12-31
FIU20030476U0 (fi) 2003-12-17
HK1064671A1 (en) 2005-02-04
EP1309555A1 (de) 2003-05-14
US20030199559A1 (en) 2003-10-23
DE20115704U1 (de) 2002-02-14
PL362660A1 (en) 2004-11-02
AT7109U2 (de) 2004-10-25
WO2002053542A1 (en) 2002-07-11
AT7110U3 (de) 2005-05-25
AP2003002820A0 (en) 2003-06-30

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Legal Events

Date Code Title Description
8363 Opposition against the patent
8331 Complete revocation