ES2069446T3 - Preparacion de hidrocloruro de ranitidina en forma 1. - Google Patents
Preparacion de hidrocloruro de ranitidina en forma 1.Info
- Publication number
- ES2069446T3 ES2069446T3 ES93304182T ES93304182T ES2069446T3 ES 2069446 T3 ES2069446 T3 ES 2069446T3 ES 93304182 T ES93304182 T ES 93304182T ES 93304182 T ES93304182 T ES 93304182T ES 2069446 T3 ES2069446 T3 ES 2069446T3
- Authority
- ES
- Spain
- Prior art keywords
- hypochloride
- ranitidine
- preparation
- solvent
- prepared
- 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.)
- Expired - Lifetime
Links
- 229960001520 ranitidine hydrochloride Drugs 0.000 title 1
- GGWBHVILAJZWKJ-KJEVSKRMSA-N ranitidine hydrochloride Chemical compound [H+].[Cl-].[O-][N+](=O)\C=C(/NC)NCCSCC1=CC=C(CN(C)C)O1 GGWBHVILAJZWKJ-KJEVSKRMSA-N 0.000 title 1
- WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Chemical compound Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 abstract 4
- VMXUWOKSQNHOCA-LCYFTJDESA-N ranitidine Chemical compound [O-][N+](=O)/C=C(/NC)NCCSCC1=CC=C(CN(C)C)O1 VMXUWOKSQNHOCA-LCYFTJDESA-N 0.000 abstract 3
- 229960000620 ranitidine Drugs 0.000 abstract 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- 239000013078 crystal Substances 0.000 abstract 1
- 238000002425 crystallisation Methods 0.000 abstract 1
- 230000008025 crystallization Effects 0.000 abstract 1
- GGWBHVILAJZWKJ-UHFFFAOYSA-N dimethyl-[[5-[2-[[1-(methylamino)-2-nitroethenyl]amino]ethylsulfanylmethyl]furan-2-yl]methyl]azanium;chloride Chemical compound Cl.[O-][N+](=O)C=C(NC)NCCSCC1=CC=C(CN(C)C)O1 GGWBHVILAJZWKJ-UHFFFAOYSA-N 0.000 abstract 1
- 239000012458 free base Substances 0.000 abstract 1
- 239000012046 mixed solvent Substances 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 239000011877 solvent mixture Substances 0.000 abstract 1
- YXFVVABEGXRONW-CNRUNOGKSA-N tritiomethylbenzene Chemical compound [3H]CC1=CC=CC=C1 YXFVVABEGXRONW-CNRUNOGKSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/38—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D307/52—Radicals substituted by nitrogen atoms not forming part of a nitro radical
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Furan Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Saccharide Compounds (AREA)
Abstract
SE PREPARA HIPOCLORURO DE RANITIDINA DE FORMA PURA 1 POR UN PROCESO DE CRISTALIZACION DE UNA SOLUCION DE HIPOCLORURO DE RANITINA EN UN SOLVENTE MEZCLADO QUE COMPRENDE 1 PARTE POR VOLUMEN DE AL MENOS UN ALCANOL INFERIOR TAL COMO UN ETANOL Y 1 20 PARTES POR VOLUMEN DE UN HIDROCARBURO AROMATICO C6-C10 TAL COMO TOLUENO, Y EN PRESENCIA DE CRISTALES DE SEMILLAS DE HIPOCLORURO DE RANITIDINA DE FORMA PURA !. EN EL PROCESO PREFERIDO DE ACUERDO CON LA INVENCION, EL HIPOCLORURO DE RANITIDINA SE PREPARA IN SITU EN LA MEZCLA DE SOLVENTE AÑADIENDO ACIDO HIDROCLORICO A UNA SOLUCION DE LA BASE LIBRE EN LA MEZCLA DE SOLVENTE, EN PRESENCIA DE CRISTALES DE SEMILLAS.
Applications Claiming Priority (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/041,354 US5338871A (en) | 1991-12-20 | 1993-04-01 | Preparation of form 1 ranitidine hydrochloride |
EP93304182A EP0626381B1 (en) | 1993-04-01 | 1993-05-28 | Preparation of form 1 ranitidine hydrochloride |
CA002099530A CA2099530C (en) | 1993-04-01 | 1993-07-02 | Preparation of form 1 ranitidine hydrochloride |
AU41794/93A AU674006B2 (en) | 1993-04-01 | 1993-07-06 | Preparation of form 1 ranitidine hydrochloride |
HU9301980A HU214334B (hu) | 1993-04-01 | 1993-07-08 | Eljárás ranitidin-hidroklorid 1 kristályformájának előállítására |
ZA934995A ZA934995B (en) | 1993-04-01 | 1993-07-12 | Preparation of form 1 ranitidine hydrochloride |
NZ260551A NZ260551A (en) | 1993-04-01 | 1994-05-18 | Preparation of form 1 ranitidine hcl crystals |
Publications (1)
Publication Number | Publication Date |
---|---|
ES2069446T3 true ES2069446T3 (es) | 1995-05-01 |
Family
ID=27560579
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES93304182T Expired - Lifetime ES2069446T3 (es) | 1993-04-01 | 1993-05-28 | Preparacion de hidrocloruro de ranitidina en forma 1. |
Country Status (11)
Country | Link |
---|---|
US (1) | US5338871A (es) |
EP (1) | EP0626381B1 (es) |
AT (1) | ATE119894T1 (es) |
AU (1) | AU674006B2 (es) |
CA (1) | CA2099530C (es) |
DE (1) | DE69300088T2 (es) |
DK (1) | DK0626381T3 (es) |
ES (1) | ES2069446T3 (es) |
HU (1) | HU214334B (es) |
NZ (1) | NZ260551A (es) |
ZA (1) | ZA934995B (es) |
Families Citing this family (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4341310A1 (de) * | 1993-12-03 | 1995-06-08 | Hexal Pharma Gmbh | Tablette oder Kapsel mit einem Gehalt an stabilem Ranitidinhydrochlorid Form 1 |
CA2120874E (en) * | 1994-04-08 | 2002-01-08 | Keshava Murthy | Form of form 1 ranitidine |
US5670671A (en) * | 1994-04-08 | 1997-09-23 | Brantford Chemicals Inc. | Process for the production of an improved form of form 1 ranitidine |
NZ272054A (en) * | 1994-05-13 | 1996-05-28 | Ranbaxy Lab Ltd | Process for producing form 1 ranitidine hydrochloride |
IN181699B (es) * | 1994-05-13 | 1998-09-05 | Ranbaxy Lab Ltd | |
DE69504156T2 (de) * | 1994-06-24 | 1998-12-24 | Ranbaxy Laboratories, Ltd., New Delhi | Verfahren zur Herstellung von Ranitidinhydrochlorid in der Kristallform 1 |
WO1996019232A1 (en) * | 1994-12-19 | 1996-06-27 | Lauteral Limited | Combinations of ranitidine hydrochloride-form 1 and bismuth compounds |
US5663381A (en) * | 1995-04-21 | 1997-09-02 | Hexal Pharmaceuticals, Inc. | Process for preparing form 1 ranitidine hydrochloride |
US5686588A (en) * | 1995-08-16 | 1997-11-11 | Yoo; Seo Hong | Amine acid salt compounds and process for the production thereof |
DE69739561D1 (de) | 1996-06-13 | 2009-10-15 | Sumitomo Chemical Co | Piperidin Derivative als Zwischenprodukte zur Herstellung von Paroxetine und Verfahren zu ihrer Herstellung |
US20020151729A1 (en) * | 1997-02-26 | 2002-10-17 | Cheng Wen J. | Novel process for the preparation of form 1 ranitidine hydrochloride |
IE990387A1 (en) * | 1998-06-17 | 2000-12-13 | Russinsky Ltd | A ranitidine base water adduct |
IT1317858B1 (it) | 2000-02-29 | 2003-07-15 | Pharmexcel S R L | Allomorfo del cloridrato dell'isomero z di derivato dialchilamminofurano, procedimento per la sua produzione e composizione |
DE102006015960A1 (de) * | 2006-04-04 | 2007-10-11 | Qiagen Gmbh | Gemisch reversibel inhibierter Enzyme |
JP2013533866A (ja) * | 2010-06-17 | 2013-08-29 | ドクター レディズ ラボラトリーズ リミテッド | 3−アミノピペリジンジヒドロクロリドの単一の鏡像異性体を調製するための方法 |
WO2015155297A1 (en) | 2014-04-11 | 2015-10-15 | Sanovel Ilac Sanayi Ve Ticaret A.S. | Pharmaceutical combinations of dabigatran and h2-receptor antagonists |
WO2015169957A1 (en) | 2014-05-09 | 2015-11-12 | Sanovel Ilac Sanayi Ve Ticaret A.S. | Pharmaceutical combinations of rivaroxaban and h2-receptor antagonists |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA1181084A (en) * | 1980-01-08 | 1985-01-15 | Glaxo Group Limited | Process for the preparation of a furan derivative |
GB2084580B (en) * | 1980-10-01 | 1984-07-04 | Glaxo Group Ltd | Aminoalkyl furan derivative |
IL63968A (en) * | 1980-10-01 | 1985-10-31 | Glaxo Group Ltd | Form 2 ranitidine hydrochloride,its preparation and pharmaceutical compositions containing it |
DE3211127C1 (de) * | 1982-03-26 | 1983-08-11 | Degussa Ag, 6000 Frankfurt | Verfahren zur Gewinnung von S-(Carboxymethyl)-(R)-cystein und S-(Carboxymethyl)-(S)-cystein |
US4613688A (en) * | 1982-04-02 | 1986-09-23 | Showa Denko Kabushiki Kaisha | Optical resolution process for DL-cysteine |
JPH0730064B2 (ja) * | 1989-08-17 | 1995-04-05 | 協和醗酵工業株式会社 | フラン誘導体 |
-
1993
- 1993-04-01 US US08/041,354 patent/US5338871A/en not_active Expired - Fee Related
- 1993-05-28 AT AT93304182T patent/ATE119894T1/de not_active IP Right Cessation
- 1993-05-28 ES ES93304182T patent/ES2069446T3/es not_active Expired - Lifetime
- 1993-05-28 DK DK93304182.4T patent/DK0626381T3/da active
- 1993-05-28 EP EP93304182A patent/EP0626381B1/en not_active Expired - Lifetime
- 1993-05-28 DE DE69300088T patent/DE69300088T2/de not_active Expired - Fee Related
- 1993-07-02 CA CA002099530A patent/CA2099530C/en not_active Expired - Fee Related
- 1993-07-06 AU AU41794/93A patent/AU674006B2/en not_active Ceased
- 1993-07-08 HU HU9301980A patent/HU214334B/hu not_active IP Right Cessation
- 1993-07-12 ZA ZA934995A patent/ZA934995B/xx unknown
-
1994
- 1994-05-18 NZ NZ260551A patent/NZ260551A/en unknown
Also Published As
Publication number | Publication date |
---|---|
AU674006B2 (en) | 1996-12-05 |
ATE119894T1 (de) | 1995-04-15 |
ZA934995B (en) | 1994-02-11 |
HU9301980D0 (en) | 1993-09-28 |
DE69300088T2 (de) | 1995-08-31 |
HUT68736A (en) | 1995-04-27 |
EP0626381A1 (en) | 1994-11-30 |
CA2099530C (en) | 2002-10-08 |
NZ260551A (en) | 1995-02-24 |
HU214334B (hu) | 1998-03-02 |
EP0626381B1 (en) | 1995-03-15 |
CA2099530A1 (en) | 1995-01-03 |
AU4179493A (en) | 1995-01-27 |
DE69300088D1 (de) | 1995-04-20 |
DK0626381T3 (da) | 1995-10-02 |
US5338871A (en) | 1994-08-16 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
ES2069446T3 (es) | Preparacion de hidrocloruro de ranitidina en forma 1. | |
NO20026094L (no) | Kondenserte azepinderivater og deres anvendelse som antidiuretiske midler | |
ECSP034691A (es) | Inhibidores de piridina de metaloproteinasas de la matriz | |
NO20042031L (no) | Syntese av syklosporin analoger | |
ES2054872T3 (es) | Nuevos derivados de acido bencimidazolin-2-oxo-1-carboxilico utiles como antagonistas de los receptores 5-ht. | |
MXPA03004920A (es) | Pirimidinas inhibidoras de metaloproteinasas de matriz. | |
CA2432578A1 (en) | Quinazolone derivatives as alpha 1a/b adrenergic receptor antagonists | |
ES2159491A1 (es) | Base cristalina de citalopram | |
GB0115515D0 (en) | Oxytocin agonisys | |
ES2058265T3 (es) | Piperidinas antagonistas de opiaceos. | |
ES2199696A1 (es) | Mezclas de estabilizantes | |
ES2046671T3 (es) | Un procedimiento para la preparacion de tetrahidroimidazo(1,4)benzodiazepin-2-tionas. | |
WO2001092392A3 (en) | Stabilizer mixtures | |
KR950032183A (ko) | 글루코피라노사이드 벤조티오펜 | |
JPS6431727A (en) | Dissolution of argininamide and drug composition containing argininamides | |
TW231289B (en) | Preparation of form 1 ranitidine hydrochloride | |
GT199800198A (es) | Formatermodinamicamenteestabledelacido(r)-3-[[(4-fluorofenil)sulfonil]amino]-1,2,3,4-tetrahidro-9h-carbazol-9-propanoico(ramatroban ). | |
ES2136198T3 (es) | Composiciones rectales que contienen odansetron en forma de su base libre. | |
ES2114231T3 (es) | Procedimiento para la produccion de una sal de adicion de acido del isomero z de un compuesto de trifeniletileno. | |
HUP0202865A2 (hu) | Eljárás 2-cianopiridin-származékok előállítására | |
KR910004652A (ko) | 5-α-환원 효소억제제로서의 3-치환된 니트로-스테로이드 유도체 | |
AR032341A1 (es) | N-(2-metansulfonil-etil)-n-hidroxiformamidas, su uso en la produccion de medicamentos, composiciones farmaceuticas que las contienen, procedimiento para preparar dichos compuestos e intermediarios para su preparacion | |
CO5070688A1 (es) | Procedimiento para la cristalizacion de un derivado tetrahidropiridina, a las nuevas formas cristalinas asi obtenidas y a las composiciones farmaceuticas que contienen | |
MX9306821A (es) | Derivados de carboxamida. | |
YU32904A (sh) | Novi analog ciklosporina za formiranje mikroemulzionih prekoncentrata |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FG2A | Definitive protection |
Ref document number: 626381 Country of ref document: ES |